Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80254 |
| ensemblid | ENSG00000182923.20 |
| hgncid | 25815 |
| symbol | CEP63 |
| name | centrosomal protein 63 |
| refseq_nuc | NM_001353108.3 |
| refseq_prot | NP_001340037.1 |
| ensembl_nuc | ENST00000675561.1 |
| ensembl_prot | ENSP00000502085.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 134486057 |
| end | 134565031 |
| strand | + |
| ver | v1.2 |
| region | chr3:134486057-134565031 |
| region5000 | chr3:134481057-134570031 |
| regionname0 | CEP63_chr3_134486057_134565031 |
| regionname5000 | CEP63_chr3_134481057_134570031 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 703 | 230 | 80 | 34 | 75 | 9 | 31 | 62 | CEP63_chr3_134481057_134570031 | CEP63 | MEALL others(698): Show |
chr3 | 134481057 | 134570031 |
| a0002 | 0/1 | 703 | 85 | 4 | 18 | 52 | 4 | 6 | 41 | CEP63_chr3_134481057_134570031 | CEP63 | MEALL others(698): Show |
chr3 | 134481057 | 134570031 |
| a0003 | 0/0 | 703 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | MEALL others(698): Show |
chr3 | 134481057 | 134570031 |
| a0004 | 0/0 | 703 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | MEALL others(698): Show |
chr3 | 134481057 | 134570031 |
| a0005 | 0/0 | 703 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | MEALL others(698): Show |
chr3 | 134481057 | 134570031 |
| a0006 | 0/0 | 703 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | MEALL others(698): Show |
chr3 | 134481057 | 134570031 |
| a0007 | 0/0 | 703 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | MEALL others(698): Show |
chr3 | 134481057 | 134570031 |
| a0008 | 0/0 | 703 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | MEALL others(698): Show |
chr3 | 134481057 | 134570031 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2109 | 167 | 68 | 22 | 50 | 6 | 20 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0001c0003 | 0/0 | 2109 | 59 | 12 | 12 | 22 | 2 | 11 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0001c0004 | 0/0 | 2109 | 3 | 0 | 0 | 3 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0001c0010 | 0/0 | 2109 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0002c0002 | 0/1 | 2109 | 82 | 4 | 18 | 49 | 4 | 6 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0002c0005 | 0/0 | 2109 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0002c0011 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0003c0006 | 0/0 | 2109 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0004c0007 | 0/0 | 2109 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0005c0013 | 0/0 | 2109 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0006c0012 | 0/0 | 2109 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0007c0008 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 | ||
| a0008c0009 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | ATGGA others(2104): Show |
chr3 | 134481057 | 134570031 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5779 | 36 | 21 | 4 | 1 | 2 | 8 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0002 | 0/0 | 5779 | 57 | 18 | 10 | 24 | 1 | 4 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0004 | 0/0 | 5779 | 25 | 0 | 0 | 17 | 1 | 7 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0005 | 0/0 | 5779 | 9 | 0 | 0 | 8 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0006 | 0/0 | 5779 | 8 | 2 | 4 | 0 | 2 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0007 | 0/0 | 5780 | 4 | 4 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5775): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0009 | 0/0 | 5779 | 4 | 3 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0010 | 0/0 | 5779 | 3 | 3 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0011 | 0/0 | 5779 | 3 | 3 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0012 | 0/0 | 5779 | 3 | 2 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0013 | 1/0 | 5779 | 3 | 2 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0014 | 0/0 | 5779 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0015 | 0/0 | 5779 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0017 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0018 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0019 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0020 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0021 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0024 | 0/0 | 5780 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5775): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0025 | 0/0 | 5780 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5775): Show |
chr3 | 134481057 | 134570031 |
| a0001c0001t0029 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0003t0001 | 0/0 | 5779 | 12 | 11 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0003t0003 | 0/0 | 5779 | 40 | 0 | 8 | 21 | 2 | 9 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0003t0008 | 0/0 | 5779 | 4 | 0 | 2 | 0 | 0 | 2 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0003t0023 | 0/0 | 5779 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0003t0027 | 0/0 | 5779 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0003t0028 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0004t0003 | 0/0 | 5779 | 3 | 0 | 0 | 3 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0001c0010t0001 | 0/0 | 5779 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0002c0002t0001 | 0/1 | 5779 | 80 | 4 | 18 | 47 | 4 | 6 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0002c0002t0022 | 0/0 | 5779 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0002c0002t0026 | 0/0 | 5794 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5789): Show |
chr3 | 134481057 | 134570031 |
| a0002c0005t0001 | 0/0 | 5779 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0002c0011t0001 | 0/0 | 5779 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0003c0006t0001 | 0/0 | 5779 | 2 | 1 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0004c0007t0003 | 0/0 | 5779 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0005c0013t0007 | 0/0 | 5780 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5775): Show |
chr3 | 134481057 | 134570031 |
| a0006c0012t0016 | 0/0 | 5779 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0007c0008t0003 | 0/0 | 5779 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| a0008c0009t0001 | 0/0 | 5779 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | GTTCA others(5774): Show |
chr3 | 134481057 | 134570031 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0012g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0013g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0014g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0015g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0015g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0017g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0018g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0019g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0020g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0021g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0024g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0025g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0001t0029g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0008g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0008g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0023g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0027g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0003t0028g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0004t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0001c0010t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0022g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0002t0026g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0002c0011t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0003c0006t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0003c0006t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0004c0007t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0005c0013t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0006c0012t0016g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0007c0008t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| a0008c0009t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0095 | EUR | GBR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0272 | EUR | GBR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | GBR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | GBR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00280 | hp1 | a0004 | c0007 | t0003 | g0186 | EUR | FIN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | FIN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0271 | EUR | FIN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00323 | hp2 | a0001 | c0010 | t0001 | g0290 | EUR | FIN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00423 | hp1 | a0001 | c0004 | t0003 | g0190 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00733 | hp1 | a0001 | c0003 | t0003 | g0155 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00735 | hp2 | a0001 | c0003 | t0027 | g0163 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0250 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0204 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01081 | hp1 | a0001 | c0003 | t0003 | g0205 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0261 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0311 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01106 | hp1 | a0001 | c0003 | t0003 | g0172 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01106 | hp2 | a0001 | c0001 | t0014 | g0033 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01109 | hp1 | a0003 | c0006 | t0001 | g0222 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01109 | hp2 | a0005 | c0013 | t0007 | g0112 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01169 | hp1 | a0001 | c0001 | t0015 | g0144 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0073 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0213 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01192 | hp2 | a0001 | c0003 | t0003 | g0154 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0097 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0228 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01256 | hp2 | a0001 | c0003 | t0008 | g0007 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01258 | hp2 | a0001 | c0003 | t0008 | g0007 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0082 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0297 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0296 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0282 | EUR | IBS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0187 | EUR | IBS | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0087 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0086 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0169 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02015 | hp1 | a0001 | c0003 | t0003 | g0165 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0105 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0183 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02071 | hp2 | a0001 | c0003 | t0023 | g0173 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0134 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | CDX | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0174 | EAS | CDX | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0091 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0194 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0090 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02523 | hp1 | a0001 | c0003 | t0003 | g0191 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | KHV | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0117 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0099 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0162 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02622 | hp1 | a0001 | c0001 | t0021 | g0108 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02630 | hp2 | a0001 | c0003 | t0028 | g0164 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0034 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02683 | hp2 | a0001 | c0003 | t0003 | g0179 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0236 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02698 | hp2 | a0001 | c0003 | t0003 | g0197 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02717 | hp1 | a0001 | c0001 | t0024 | g0113 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02735 | hp2 | a0001 | c0003 | t0003 | g0160 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02738 | hp1 | a0001 | c0003 | t0008 | g0199 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02738 | hp2 | a0006 | c0012 | t0016 | g0093 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02818 | hp1 | a0001 | c0001 | t0025 | g0119 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02818 | hp2 | a0003 | c0006 | t0001 | g0220 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0032 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0111 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0049 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0106 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0141 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0088 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0094 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03491 | hp2 | a0001 | c0003 | t0003 | g0170 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03492 | hp1 | a0001 | c0003 | t0003 | g0171 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | MSL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0045 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03669 | hp2 | a0001 | c0003 | t0008 | g0180 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0121 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03704 | hp2 | a0001 | c0003 | t0003 | g0175 | SAS | PJL | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0177 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0280 | SAS | BEB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04204 | hp1 | a0001 | c0003 | t0003 | g0176 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0043 | SAS | STU | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | CHB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | CHB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0115 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18947 | hp1 | a0007 | c0008 | t0003 | g0182 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18949 | hp2 | a0002 | c0005 | t0001 | g0159 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18950 | hp1 | a0002 | c0005 | t0001 | g0178 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18951 | hp1 | a0001 | c0003 | t0003 | g0181 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0167 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18966 | hp2 | a0002 | c0002 | t0022 | g0246 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0156 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18986 | hp2 | a0001 | c0003 | t0003 | g0188 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0203 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18998 | hp2 | a0001 | c0003 | t0003 | g0195 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18999 | hp1 | a0001 | c0003 | t0003 | g0185 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19000 | hp2 | a0001 | c0004 | t0003 | g0192 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19003 | hp2 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19010 | hp2 | a0001 | c0003 | t0003 | g0184 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19030 | hp1 | a0001 | c0001 | t0020 | g0092 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19043 | hp1 | a0001 | c0001 | t0029 | g0136 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19043 | hp2 | a0008 | c0009 | t0001 | g0135 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19060 | hp1 | a0002 | c0011 | t0001 | g0294 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19065 | hp1 | a0001 | c0003 | t0003 | g0158 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19076 | hp1 | a0001 | c0003 | t0003 | g0200 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0166 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19082 | hp2 | a0002 | c0002 | t0026 | g0304 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19083 | hp2 | a0001 | c0004 | t0003 | g0193 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19085 | hp1 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19091 | hp2 | a0001 | c0003 | t0003 | g0201 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | YRI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0030 | AFR | ASW | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | ASW | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0245 | EUR | TSI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0080 | EUR | TSI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0081 | EUR | TSI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20805 | hp2 | a0001 | c0003 | t0003 | g0161 | EUR | TSI | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01123 | hp1 | a0001 | c0003 | t0003 | g0168 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG01123 | hp2 | a0001 | c0001 | t0012 | g0107 | AMR | CLM | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02109 | hp1 | a0001 | c0001 | t0019 | g0061 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0098 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0109 | AFR | ACB | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0110 | AFR | USA | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0145 | AFR | USA | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | USA | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | USA | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | LWK | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0291 | REF | REF | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0048 | REF | REF | CEP63_chr3_134481057_134570031 | CEP63 | chr3 | 134481057 | 134570031 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134537268 | G | C | 1 | a0004 | 1 | HG00280.hp1 | missense_variant&splice_region_variant | MODERATE | c.555G>C | p.Gln185His | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/15 | 726/5779 | 555/2112 | 185/703 | chr3 | 134537268 | |||
| chr3:134546264 | C | G | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.905C>G | p.Thr302Ser | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/15 | 1076/5779 | 905/2112 | 302/703 | chr3 | 134546264 | |||
| chr3:134549149 | C | A | 1 | a0003 | 2 | HG01109.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.1155C>A | p.Asn385Lys | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/15 | 1326/5779 | 1155/2112 | 385/703 | chr3 | 134549149 | |||
| chr3:134550200 | C | A | 1 | a0007 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.1320C>A | p.Asp440Glu | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/15 | 1491/5779 | 1320/2112 | 440/703 | chr3 | 134550200 | |||
| chr3:134559181 | A | T | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1705A>T | p.Ile569Leu | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/15 | 1876/5779 | 1705/2112 | 569/703 | chr3 | 134559181 | |||
| chr3:134559308 | C | T | 1 | a0006 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1832C>T | p.Ser611Phe | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/15 | 2003/5779 | 1832/2112 | 611/703 | chr3 | 134559308 | |||
| chr3:134559428 | C | T | 1 | a0002 | 84 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(81): Show |
missense_variant&splice_region_variant | MODERATE | c.1952C>T | p.Ser651Leu | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/15 | 2123/5779 | 1952/2112 | 651/703 | chr3 | 134559428 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134507127 | T | C | 6 | a0001c0003 a0001c0004 a0002c0005 others(3): Show |
67 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(64): Show |
synonymous_variant | LOW | c.63T>C | p.Cys21Cys | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/15 | 234/5779 | 63/2112 | 21/703 | chr3 | 134507127 | |||
| chr3:134545597 | C | A | 1 | a0001c0004 | 3 | HG00423.hp1 NA19000.hp2 NA19083.hp2 |
synonymous_variant | LOW | c.567C>A | p.Val189Val | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/15 | 738/5779 | 567/2112 | 189/703 | chr3 | 134545597 | |||
| chr3:134547380 | G | A | 1 | a0001c0010 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.975G>A | p.Gly325Gly | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/15 | 1146/5779 | 975/2112 | 325/703 | chr3 | 134547380 | |||
| chr3:134550146 | G | A | 1 | a0002c0011 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.1266G>A | p.Gln422Gln | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/15 | 1437/5779 | 1266/2112 | 422/703 | chr3 | 134550146 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134486068 | C | T | 1 | a0001c0001t0029 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-160C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/15 | chr3 | 134486068 | |||||||
| chr3:134486144 | C | G | 1 | a0001c0001t0009 | 4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-84C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/15 | 9177 | chr3 | 134486144 | ||||||
| chr3:134561553 | T | A | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*18T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 18 | chr3 | 134561553 | ||||||
| chr3:134561696 | A | G | 2 | a0001c0003t0027 a0001c0003t0028 |
2 | HG00735.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*161A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 161 | chr3 | 134561696 | ||||||
| chr3:134561943 | TACCTGGA others(7): Show |
T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*411_*424delCTGGAT others(8): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 411 | INFO_REALIGN_3_PRIME | chr3 | 134561943 | |||||
| chr3:134562055 | A | T | 1 | a0001c0003t0028 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*520A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 520 | chr3 | 134562055 | ||||||
| chr3:134562076 | C | CT | 4 | a0001c0001t0007 a0001c0001t0024 a0001c0001t0025 others(1): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*542dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 543 | INFO_REALIGN_3_PRIME | chr3 | 134562076 | |||||
| chr3:134562106 | G | T | 27 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(24): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*571G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 571 | chr3 | 134562106 | ||||||
| chr3:134562193 | A | G | 1 | a0001c0003t0023 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*658A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 658 | chr3 | 134562193 | ||||||
| chr3:134562232 | G | A | 1 | a0006c0012t0016 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 697 | chr3 | 134562232 | ||||||
| chr3:134562409 | T | A | 2 | a0001c0001t0014 a0001c0001t0017 |
3 | HG01106.hp2 HG02647.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*874T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 874 | chr3 | 134562409 | ||||||
| chr3:134562500 | C | T | 1 | a0001c0001t0025 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 965 | chr3 | 134562500 | ||||||
| chr3:134562689 | C | T | 1 | a0001c0001t0006 | 8 | HG01175.hp1 HG01261.hp1 HG01346.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1154C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1154 | chr3 | 134562689 | ||||||
| chr3:134562884 | C | T | 4 | a0001c0001t0007 a0001c0001t0024 a0001c0001t0025 others(1): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1349C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1349 | chr3 | 134562884 | ||||||
| chr3:134562977 | T | C | 1 | a0001c0001t0018 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1442 | chr3 | 134562977 | ||||||
| chr3:134563020 | C | T | 8 | a0001c0003t0003 a0001c0003t0008 a0001c0003t0023 others(5): Show |
52 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1485C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1485 | chr3 | 134563020 | ||||||
| chr3:134563035 | G | A | 1 | a0001c0001t0017 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1500G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1500 | chr3 | 134563035 | ||||||
| chr3:134563046 | T | C | 2 | a0001c0001t0014 a0001c0001t0017 |
3 | HG01106.hp2 HG02647.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1511T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1511 | chr3 | 134563046 | ||||||
| chr3:134563139 | A | T | 1 | a0001c0001t0015 | 2 | HG01169.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1604A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1604 | chr3 | 134563139 | ||||||
| chr3:134563169 | T | C | 1 | a0001c0001t0010 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1634T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1634 | chr3 | 134563169 | ||||||
| chr3:134563437 | T | G | 27 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(24): Show |
214 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*1902T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 1902 | chr3 | 134563437 | ||||||
| chr3:134563564 | A | G | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(5): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*2029A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2029 | chr3 | 134563564 | ||||||
| chr3:134563642 | C | T | 2 | a0001c0001t0010 a0001c0001t0024 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2107C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2107 | chr3 | 134563642 | ||||||
| chr3:134563914 | T | C | 1 | a0001c0003t0008 | 4 | HG01256.hp2 HG01258.hp2 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2379T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2379 | chr3 | 134563914 | ||||||
| chr3:134563954 | C | G | 26 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(23): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*2419C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2419 | chr3 | 134563954 | ||||||
| chr3:134563963 | C | G | 2 | a0001c0001t0012 a0001c0001t0021 |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2428C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2428 | chr3 | 134563963 | ||||||
| chr3:134564015 | A | T | 1 | a0001c0001t0011 | 3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2480A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2480 | chr3 | 134564015 | ||||||
| chr3:134564106 | T | C | 2 | a0001c0001t0011 a0001c0001t0019 |
4 | HG02109.hp1 HG02559.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2571T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2571 | chr3 | 134564106 | ||||||
| chr3:134564337 | A | C | 1 | a0001c0001t0004 | 25 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2802A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2802 | chr3 | 134564337 | ||||||
| chr3:134564409 | C | A | 1 | a0001c0001t0005 | 9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2874C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2874 | chr3 | 134564409 | ||||||
| chr3:134564474 | T | C | 1 | a0001c0001t0020 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2939T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 2939 | chr3 | 134564474 | ||||||
| chr3:134564576 | G | GATGCTGG others(22): Show |
1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3044_*3045insCTGG others(25): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3045 | INFO_REALIGN_3_PRIME | chr3 | 134564576 | |||||
| chr3:134564582 | A | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3047A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3047 | chr3 | 134564582 | ||||||
| chr3:134564587 | C | G | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3052C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3052 | chr3 | 134564587 | ||||||
| chr3:134564590 | C | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3055C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3055 | chr3 | 134564590 | ||||||
| chr3:134564635 | C | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3100C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3100 | chr3 | 134564635 | ||||||
| chr3:134564642 | G | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3107G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3107 | chr3 | 134564642 | ||||||
| chr3:134564653 | T | C | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3118T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3118 | chr3 | 134564653 | ||||||
| chr3:134564670 | T | G | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3135T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3135 | chr3 | 134564670 | ||||||
| chr3:134564673 | G | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3138G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3138 | chr3 | 134564673 | ||||||
| chr3:134564674 | A | G | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3139A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3139 | chr3 | 134564674 | ||||||
| chr3:134564683 | T | A | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3148T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3148 | chr3 | 134564683 | ||||||
| chr3:134564686 | A | C | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3151A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3151 | chr3 | 134564686 | ||||||
| chr3:134564693 | A | G | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3158A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3158 | chr3 | 134564693 | ||||||
| chr3:134564694 | G | T | 1 | a0002c0002t0026 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3159G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3159 | chr3 | 134564694 | ||||||
| chr3:134564706 | T | C | 1 | a0001c0001t0012 | 3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3171T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 15/15 | 3171 | chr3 | 134564706 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:134486207 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.-26+5C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486207 | |||||||
| chr3:134486229 | G | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-26+27G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486229 | |||||||
| chr3:134486371 | C | G | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-26+169C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486371 | |||||||
| chr3:134486385 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(208): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-26+183C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486385 | |||||||
| chr3:134486389 | C | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(208): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-26+187C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486389 | |||||||
| chr3:134486587 | C | T | 1 | a0001c0001t0004g0102 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-26+385C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486587 | |||||||
| chr3:134486603 | ACCTT | A | 196 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(193): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-26+406_-26+409del others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134486603 | ||||||
| chr3:134486620 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-26+418A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486620 | |||||||
| chr3:134486970 | G | C | 1 | a0001c0001t0002g0009 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-26+768G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134486970 | |||||||
| chr3:134487078 | A | G | 191 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(188): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-26+876A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487078 | |||||||
| chr3:134487115 | A | G | 3 | a0001c0001t0004g0094 a0001c0001t0004g0095 a0001c0001t0004g0096 |
3 | HG00099.hp1 HG02683.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-26+913A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487115 | |||||||
| chr3:134487207 | G | C | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-26+1005G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487207 | |||||||
| chr3:134487227 | A | G | 191 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(188): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-26+1025A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487227 | |||||||
| chr3:134487474 | G | T | 1 | a0002c0002t0001g0311 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-26+1272G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487474 | |||||||
| chr3:134487569 | A | G | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-26+1367A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487569 | |||||||
| chr3:134487574 | A | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+1372A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487574 | |||||||
| chr3:134487886 | T | C | 205 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(202): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-26+1684T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487886 | |||||||
| chr3:134487907 | T | C | 205 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(202): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-26+1705T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487907 | |||||||
| chr3:134487920 | A | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-26+1718A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487920 | |||||||
| chr3:134487954 | A | G | 1 | a0006c0012t0016g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-26+1752A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134487954 | |||||||
| chr3:134488003 | G | A | 214 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(211): Show |
219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-26+1801G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488003 | |||||||
| chr3:134488151 | C | T | 1 | a0002c0002t0001g0308 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-26+1949C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488151 | |||||||
| chr3:134488235 | G | A | 191 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(188): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-26+2033G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488235 | |||||||
| chr3:134488274 | T | C | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+2072T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488274 | |||||||
| chr3:134488292 | C | A | 84 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(81): Show |
86 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.-26+2090C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488292 | |||||||
| chr3:134488424 | T | G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26+2222T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488424 | |||||||
| chr3:134488616 | A | G | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 |
3 | HG00280.hp2 HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-26+2414A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488616 | |||||||
| chr3:134488745 | G | A | 7 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 others(4): Show |
7 | HG01123.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26+2543G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488745 | |||||||
| chr3:134488801 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG01891.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-26+2599C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488801 | |||||||
| chr3:134488837 | GTTAA | G | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26+2640_-26+2643d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134488837 | ||||||
| chr3:134488844 | A | T | 53 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 others(50): Show |
54 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-26+2642A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488844 | |||||||
| chr3:134488877 | G | A | 5 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(2): Show |
5 | NA18941.hp2 NA18955.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+2675G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134488877 | |||||||
| chr3:134489158 | C | CA | 20 | a0001c0001t0001g0211 a0001c0001t0001g0216 a0001c0001t0002g0015 others(17): Show |
20 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26+2978dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134489158 | ||||||
| chr3:134489158 | CA | C | 25 | a0001c0001t0004g0089 a0001c0001t0005g0128 a0001c0001t0007g0114 others(22): Show |
25 | HG01069.hp1 HG01081.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.-26+2978delA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134489158 | ||||||
| chr3:134489285 | C | T | 1 | a0001c0001t0012g0105 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-26+3083C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489285 | |||||||
| chr3:134489290 | A | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(202): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-26+3088A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489290 | |||||||
| chr3:134489325 | G | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(208): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-26+3123G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489325 | |||||||
| chr3:134489377 | G | T | 5 | a0001c0003t0001g0006 a0001c0003t0001g0150 a0001c0003t0001g0151 others(2): Show |
6 | HG00741.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+3175G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489377 | |||||||
| chr3:134489595 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-26+3393G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489595 | |||||||
| chr3:134489649 | A | G | 2 | a0001c0001t0021g0108 a0002c0002t0001g0303 |
2 | HG02622.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-26+3447A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134489649 | |||||||
| chr3:134490010 | A | C | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-26+3808A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490010 | |||||||
| chr3:134490021 | C | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+3819C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490021 | |||||||
| chr3:134490024 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0300 others(1): Show |
5 | HG00609.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+3822A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490024 | |||||||
| chr3:134490183 | A | T | 4 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 others(1): Show |
4 | HG02559.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+3981A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490183 | |||||||
| chr3:134490193 | C | G | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-26+3991C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490193 | |||||||
| chr3:134490347 | C | T | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+4145C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490347 | |||||||
| chr3:134490407 | T | G | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+4205T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490407 | |||||||
| chr3:134490460 | A | G | 2 | a0002c0002t0001g0297 a0002c0002t0001g0298 |
2 | HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-26+4258A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490460 | |||||||
| chr3:134490575 | G | GT | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+4376dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134490575 | ||||||
| chr3:134490647 | T | TCCCATAA others(8): Show |
200 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(197): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.-26+4458_-26+4472d others(17): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134490647 | ||||||
| chr3:134490700 | A | G | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-26+4498A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134490700 | |||||||
| chr3:134491114 | A | G | 26 | a0001c0001t0002g0017 a0001c0001t0002g0064 a0001c0001t0002g0065 others(23): Show |
27 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25-4182A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491114 | |||||||
| chr3:134491156 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-25-4140A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491156 | |||||||
| chr3:134491341 | A | G | 202 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(199): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-25-3955A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491341 | |||||||
| chr3:134491391 | G | A | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-25-3905G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491391 | |||||||
| chr3:134491407 | A | G | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-25-3889A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491407 | |||||||
| chr3:134491544 | A | G | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25-3752A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491544 | |||||||
| chr3:134491766 | G | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-3530G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491766 | |||||||
| chr3:134491881 | G | C | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-3415G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134491881 | |||||||
| chr3:134492070 | C | CT | 187 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(184): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-25-3205dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134492070 | ||||||
| chr3:134492070 | C | CTT | 18 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0005g0121 others(15): Show |
18 | HG02738.hp1 HG02809.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25-3206_-25-3205d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134492070 | ||||||
| chr3:134492070 | CT | C | 10 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0004g0019 others(7): Show |
10 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-3205delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134492070 | ||||||
| chr3:134492077 | T | C | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-25-3219T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492077 | |||||||
| chr3:134492166 | C | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-25-3130C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492166 | |||||||
| chr3:134492194 | C | G | 202 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(199): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-25-3102C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492194 | |||||||
| chr3:134492211 | C | T | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25-3085C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492211 | |||||||
| chr3:134492222 | C | T | 202 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(199): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-25-3074C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492222 | |||||||
| chr3:134492435 | A | G | 4 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0099 others(1): Show |
4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-2861A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492435 | |||||||
| chr3:134492480 | C | CTACT | 217 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(214): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-25-2816_-25-2815i others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492480 | |||||||
| chr3:134492572 | CT | C | 17 | a0001c0001t0002g0015 a0001c0001t0002g0021 a0001c0001t0002g0022 others(14): Show |
17 | HG00738.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-25-2707delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134492572 | ||||||
| chr3:134492604 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-25-2692A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492604 | |||||||
| chr3:134492807 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-25-2489C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492807 | |||||||
| chr3:134492865 | A | T | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-25-2431A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492865 | |||||||
| chr3:134492998 | C | T | 3 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0020g0092 |
3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-25-2298C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134492998 | |||||||
| chr3:134493030 | A | G | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-2266A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493030 | |||||||
| chr3:134493173 | C | T | 1 | a0001c0003t0003g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-25-2123C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493173 | |||||||
| chr3:134493216 | A | C | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-2080A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493216 | |||||||
| chr3:134493275 | C | T | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-2021C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493275 | |||||||
| chr3:134493284 | G | A | 1 | a0001c0001t0024g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-25-2012G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493284 | |||||||
| chr3:134493614 | A | C | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-1682A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493614 | |||||||
| chr3:134493684 | T | C | 217 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(214): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-25-1612T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493684 | |||||||
| chr3:134493744 | C | T | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-1552C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134493744 | |||||||
| chr3:134494048 | T | G | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-1248T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494048 | |||||||
| chr3:134494092 | A | ATATT | 37 | a0001c0001t0002g0009 a0001c0001t0002g0016 a0001c0001t0002g0021 others(34): Show |
38 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-25-1166_-25-1163d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | ||||||
| chr3:134494092 | A | ATATTTAT others(1): Show |
11 | a0001c0001t0002g0017 a0001c0001t0002g0029 a0001c0001t0002g0067 others(8): Show |
11 | HG01175.hp1 HG02074.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-1170_-25-1163d others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | ||||||
| chr3:134494092 | A | ATATTTAT others(5): Show |
1 | a0001c0001t0002g0066 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-25-1174_-25-1163d others(14): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | ||||||
| chr3:134494092 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-25-1204A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494092 | |||||||
| chr3:134494092 | ATATT | A | 14 | a0001c0001t0001g0221 a0001c0001t0001g0299 a0001c0001t0009g0097 others(11): Show |
14 | HG00609.hp2 HG01243.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25-1166_-25-1163d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | ||||||
| chr3:134494092 | ATATTTAT others(1): Show |
A | 192 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(189): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-25-1170_-25-1163d others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | ||||||
| chr3:134494092 | ATATTTAT others(13): Show |
A | 8 | a0001c0001t0005g0120 a0001c0001t0005g0122 a0001c0001t0005g0123 others(5): Show |
8 | NA18940.hp2 NA18951.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-1182_-25-1163d others(22): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494092 | ||||||
| chr3:134494201 | C | T | 1 | a0001c0003t0003g0196 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-25-1095C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494201 | |||||||
| chr3:134494228 | A | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-25-1068A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494228 | |||||||
| chr3:134494252 | C | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-25-1044C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494252 | |||||||
| chr3:134494281 | A | C | 1 | a0006c0012t0016g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-25-1015A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494281 | |||||||
| chr3:134494281 | AT | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-1001delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494281 | ||||||
| chr3:134494286 | T | TC | 3 | a0001c0001t0001g0129 a0001c0003t0027g0163 a0001c0003t0028g0164 |
3 | HG00735.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-25-1010_-25-1009i others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494286 | |||||||
| chr3:134494338 | ACTC | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0301 |
3 | HG03490.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-25-955_-25-953del others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 134494338 | ||||||
| chr3:134494533 | G | C | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-25-763G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494533 | |||||||
| chr3:134494614 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0028 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-25-682A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494614 | |||||||
| chr3:134494696 | C | T | 220 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(217): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-25-600C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494696 | |||||||
| chr3:134494714 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-25-582G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494714 | |||||||
| chr3:134494823 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-25-473A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494823 | |||||||
| chr3:134494869 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-25-427C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134494869 | |||||||
| chr3:134495055 | T | G | 286 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(283): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.-25-241T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495055 | |||||||
| chr3:134495077 | C | T | 1 | a0001c0003t0003g0195 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-25-219C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495077 | |||||||
| chr3:134495078 | G | A | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-218G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495078 | |||||||
| chr3:134495090 | T | A | 1 | a0001c0003t0003g0165 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-25-206T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495090 | |||||||
| chr3:134495095 | A | C | 10 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(7): Show |
12 | HG00558.hp1 HG02083.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25-201A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495095 | |||||||
| chr3:134495124 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-25-172T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495124 | |||||||
| chr3:134495139 | T | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-25-157T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495139 | |||||||
| chr3:134495200 | T | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-25-96T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 1/14 | chr3 | 134495200 | |||||||
| chr3:134495732 | C | G | 1 | a0001c0001t0002g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.44+368C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134495732 | |||||||
| chr3:134495879 | A | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+515A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134495879 | |||||||
| chr3:134496080 | A | T | 1 | a0001c0001t0002g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.44+716A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496080 | |||||||
| chr3:134496174 | A | G | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+810A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496174 | |||||||
| chr3:134496199 | A | AT | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.44+838dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496199 | ||||||
| chr3:134496210 | A | G | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.44+846A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496210 | |||||||
| chr3:134496431 | A | AG | 58 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(55): Show |
61 | HG00140.hp2 HG00738.hp2 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.44+1078dupG | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496431 | ||||||
| chr3:134496431 | AG | A | 24 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(21): Show |
24 | HG01109.hp2 HG01123.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.44+1078delG | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496431 | ||||||
| chr3:134496431 | AGG | A | 186 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(183): Show |
191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.44+1077_44+1078del others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496431 | ||||||
| chr3:134496434 | G | C | 3 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0020g0092 |
3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.44+1070G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496434 | |||||||
| chr3:134496440 | G | C | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+1076G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496440 | |||||||
| chr3:134496441 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.44+1077G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496441 | |||||||
| chr3:134496607 | G | T | 4 | a0001c0003t0003g0191 a0001c0004t0003g0190 a0001c0004t0003g0192 others(1): Show |
4 | HG00423.hp1 HG02523.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+1243G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496607 | |||||||
| chr3:134496632 | A | G | 1 | a0002c0002t0001g0298 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.44+1268A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496632 | |||||||
| chr3:134496651 | A | G | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.44+1287A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134496651 | |||||||
| chr3:134496922 | A | AT | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.44+1559dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496922 | ||||||
| chr3:134496923 | T | TC | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+1566dupC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134496923 | ||||||
| chr3:134497029 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.44+1665C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497029 | |||||||
| chr3:134497139 | G | A | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.44+1775G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497139 | |||||||
| chr3:134497297 | G | T | 217 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(214): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.44+1933G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497297 | |||||||
| chr3:134497367 | A | G | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+2003A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497367 | |||||||
| chr3:134497479 | C | T | 1 | a0001c0001t0004g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.44+2115C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497479 | |||||||
| chr3:134497496 | C | G | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG01891.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.44+2132C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497496 | |||||||
| chr3:134497511 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.44+2147A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497511 | |||||||
| chr3:134497555 | A | C | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.44+2191A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497555 | |||||||
| chr3:134497739 | A | ATT | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+2384_44+2385dup others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134497739 | ||||||
| chr3:134497801 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0286 others(11): Show |
15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+2437A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497801 | |||||||
| chr3:134497835 | C | G | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+2471C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497835 | |||||||
| chr3:134497933 | G | A | 7 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+2569G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134497933 | |||||||
| chr3:134498066 | G | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+2702G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134498066 | |||||||
| chr3:134498230 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.44+2866C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134498230 | |||||||
| chr3:134498555 | C | G | 1 | a0001c0001t0015g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.44+3191C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134498555 | |||||||
| chr3:134498683 | C | T | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+3319C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134498683 | |||||||
| chr3:134499051 | T | C | 1 | a0003c0006t0001g0222 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.44+3687T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499051 | |||||||
| chr3:134499062 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0286 others(11): Show |
15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+3698A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499062 | |||||||
| chr3:134499076 | C | T | 2 | a0002c0002t0001g0297 a0002c0002t0001g0298 |
2 | HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.44+3712C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499076 | |||||||
| chr3:134499110 | T | C | 4 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+3746T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499110 | |||||||
| chr3:134499316 | A | C | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.44+3952A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499316 | |||||||
| chr3:134499320 | T | G | 3 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0020g0092 |
3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.44+3956T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499320 | |||||||
| chr3:134499622 | G | T | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44+4258G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499622 | |||||||
| chr3:134499711 | A | G | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44+4347A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499711 | |||||||
| chr3:134499715 | T | C | 217 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(214): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.44+4351T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499715 | |||||||
| chr3:134499820 | C | CT | 20 | a0001c0001t0001g0139 a0001c0001t0002g0009 a0001c0001t0004g0295 others(17): Show |
20 | HG01123.hp2 HG01168.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.44+4477dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134499820 | ||||||
| chr3:134499820 | C | CTT | 158 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(155): Show |
162 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.44+4476_44+4477dup others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134499820 | ||||||
| chr3:134499820 | C | CTTT | 29 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0216 others(26): Show |
30 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.44+4475_44+4477dup others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134499820 | ||||||
| chr3:134499820 | CT | C | 19 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0022 others(16): Show |
19 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.44+4477delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134499820 | ||||||
| chr3:134499855 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.44+4491G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499855 | |||||||
| chr3:134499961 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0018g0030 |
2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.44+4597T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134499961 | |||||||
| chr3:134500024 | C | T | 1 | a0001c0001t0004g0020 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.44+4660C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500024 | |||||||
| chr3:134500031 | G | T | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.44+4667G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500031 | |||||||
| chr3:134500045 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.44+4681C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500045 | |||||||
| chr3:134500103 | G | A | 1 | a0001c0003t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.44+4739G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500103 | |||||||
| chr3:134500150 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.44+4786G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500150 | |||||||
| chr3:134500159 | A | G | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.44+4795A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500159 | |||||||
| chr3:134500177 | C | T | 220 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(217): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.44+4813C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500177 | |||||||
| chr3:134500292 | T | C | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+4928T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500292 | |||||||
| chr3:134500332 | C | T | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+4968C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500332 | |||||||
| chr3:134500335 | G | A | 286 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(283): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.44+4971G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500335 | |||||||
| chr3:134500398 | ACATGTGA others(3): Show |
A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+5041_44+5050del others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134500398 | ||||||
| chr3:134500444 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.44+5080C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500444 | |||||||
| chr3:134500477 | G | A | 2 | a0002c0002t0001g0224 a0002c0002t0001g0225 |
2 | HG00544.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.44+5113G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500477 | |||||||
| chr3:134500482 | G | A | 1 | a0001c0001t0002g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.44+5118G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500482 | |||||||
| chr3:134500506 | T | C | 26 | a0001c0001t0002g0017 a0001c0001t0002g0064 a0001c0001t0002g0065 others(23): Show |
27 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.44+5142T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500506 | |||||||
| chr3:134500805 | GT | G | 5 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(2): Show |
5 | HG01109.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+5450delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134500805 | ||||||
| chr3:134500862 | T | C | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.44+5498T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134500862 | |||||||
| chr3:134500977 | T | TA | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.44+5614dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134500977 | ||||||
| chr3:134501016 | A | T | 5 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(2): Show |
5 | HG01109.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+5652A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501016 | |||||||
| chr3:134501151 | C | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.44+5787C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501151 | |||||||
| chr3:134501182 | T | C | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+5818T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501182 | |||||||
| chr3:134501216 | A | G | 7 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+5852A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501216 | |||||||
| chr3:134501277 | C | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-5832C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501277 | |||||||
| chr3:134501284 | C | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45-5825C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501284 | |||||||
| chr3:134501405 | A | G | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45-5704A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501405 | |||||||
| chr3:134501479 | A | T | 1 | a0004c0007t0003g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.45-5630A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501479 | |||||||
| chr3:134501570 | A | AT | 212 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0131 others(209): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.45-5530dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134501570 | ||||||
| chr3:134501954 | T | C | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-5155T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501954 | |||||||
| chr3:134501997 | G | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-5112G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134501997 | |||||||
| chr3:134502024 | G | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-5085G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502024 | |||||||
| chr3:134502163 | G | T | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-4946G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502163 | |||||||
| chr3:134502283 | G | GT | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
97 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.45-4817dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134502283 | ||||||
| chr3:134502401 | A | G | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-4708A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502401 | |||||||
| chr3:134502597 | C | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-4512C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502597 | |||||||
| chr3:134502960 | A | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0289 a0001c0010t0001g0290 |
3 | HG00323.hp2 HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.45-4149A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502960 | |||||||
| chr3:134502981 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.45-4128A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134502981 | |||||||
| chr3:134503100 | C | CT | 200 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(197): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.45-3989dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134503100 | ||||||
| chr3:134503100 | C | CTT | 20 | a0001c0001t0002g0029 a0001c0001t0005g0120 a0001c0001t0005g0121 others(17): Show |
20 | HG01884.hp1 HG02559.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.45-3990_45-3989dup others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134503100 | ||||||
| chr3:134503130 | C | T | 3 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0020g0092 |
3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.45-3979C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503130 | |||||||
| chr3:134503250 | C | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-3859C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503250 | |||||||
| chr3:134503294 | C | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.45-3815C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503294 | |||||||
| chr3:134503319 | A | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-3790A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503319 | |||||||
| chr3:134503437 | G | T | 1 | a0001c0001t0024g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45-3672G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503437 | |||||||
| chr3:134503526 | G | C | 1 | a0001c0003t0001g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45-3583G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503526 | |||||||
| chr3:134503604 | T | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-3505T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503604 | |||||||
| chr3:134503665 | G | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-3444G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503665 | |||||||
| chr3:134503739 | C | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-3370C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503739 | |||||||
| chr3:134503840 | G | GTTTCATT others(14): Show |
1 | a0001c0001t0021g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.45-3265_45-3264ins others(21): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134503840 | ||||||
| chr3:134503840 | G | GTTTCCAT others(15): Show |
200 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(197): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.45-3264_45-3263ins others(22): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134503840 | ||||||
| chr3:134503869 | C | T | 1 | a0002c0002t0001g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.45-3240C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503869 | |||||||
| chr3:134503880 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-3229A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134503880 | |||||||
| chr3:134504003 | G | C | 1 | a0001c0003t0001g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45-3106G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504003 | |||||||
| chr3:134504113 | CT | C | 83 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(80): Show |
85 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.45-2984delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134504113 | ||||||
| chr3:134504115 | T | C | 1 | a0001c0001t0013g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.45-2994T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504115 | |||||||
| chr3:134504127 | G | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-2982G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504127 | |||||||
| chr3:134504160 | T | G | 1 | a0002c0002t0001g0298 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.45-2949T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504160 | |||||||
| chr3:134504169 | C | G | 217 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(214): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.45-2940C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504169 | |||||||
| chr3:134504176 | G | C | 217 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(214): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.45-2933G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504176 | |||||||
| chr3:134504208 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.45-2901G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504208 | |||||||
| chr3:134504256 | A | AT | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-2847dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134504256 | ||||||
| chr3:134504375 | C | G | 26 | a0001c0001t0002g0017 a0001c0001t0002g0064 a0001c0001t0002g0065 others(23): Show |
27 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.45-2734C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504375 | |||||||
| chr3:134504453 | A | G | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.45-2656A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504453 | |||||||
| chr3:134504457 | G | C | 1 | a0001c0003t0003g0167 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.45-2652G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504457 | |||||||
| chr3:134504475 | A | G | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-2634A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504475 | |||||||
| chr3:134504594 | G | A | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-2515G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504594 | |||||||
| chr3:134504706 | G | GC | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.45-2401dupC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134504706 | ||||||
| chr3:134504721 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-2388G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504721 | |||||||
| chr3:134504766 | C | G | 4 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-2343C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504766 | |||||||
| chr3:134504846 | C | G | 1 | a0002c0002t0001g0275 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.45-2263C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504846 | |||||||
| chr3:134504888 | T | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.45-2221T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504888 | |||||||
| chr3:134504966 | C | G | 11 | a0001c0001t0002g0074 a0001c0001t0002g0083 a0001c0001t0002g0084 others(8): Show |
12 | HG00140.hp2 HG01099.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-2143C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134504966 | |||||||
| chr3:134505023 | C | T | 3 | a0001c0001t0004g0039 a0001c0001t0013g0087 a0001c0001t0013g0088 |
3 | HG01884.hp1 HG02155.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.45-2086C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505023 | |||||||
| chr3:134505076 | A | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45-2033A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505076 | |||||||
| chr3:134505264 | T | A | 10 | a0002c0002t0001g0103 a0002c0002t0001g0210 a0002c0002t0001g0227 others(7): Show |
10 | HG00558.hp2 HG01255.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-1845T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505264 | |||||||
| chr3:134505322 | G | A | 2 | a0001c0003t0003g0188 a0001c0003t0003g0195 |
2 | NA18986.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.45-1787G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505322 | |||||||
| chr3:134505330 | T | G | 1 | a0002c0002t0001g0235 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.45-1779T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505330 | |||||||
| chr3:134505395 | G | A | 5 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0168 others(2): Show |
5 | HG00733.hp1 HG01123.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-1714G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505395 | |||||||
| chr3:134505399 | G | C | 5 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(2): Show |
5 | NA18941.hp2 NA18955.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-1710G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505399 | |||||||
| chr3:134505551 | C | T | 1 | a0002c0002t0001g0274 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.45-1558C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505551 | |||||||
| chr3:134505595 | G | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45-1514G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505595 | |||||||
| chr3:134505595 | G | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-1514G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505595 | |||||||
| chr3:134505659 | T | C | 1 | a0002c0002t0001g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.45-1450T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505659 | |||||||
| chr3:134505966 | C | T | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-1143C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134505966 | |||||||
| chr3:134506060 | T | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-1049T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506060 | |||||||
| chr3:134506402 | C | T | 3 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0020g0092 |
3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.45-707C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506402 | |||||||
| chr3:134506564 | G | T | 9 | a0002c0002t0001g0213 a0002c0002t0001g0217 a0002c0002t0001g0269 others(6): Show |
9 | HG00099.hp2 HG00323.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-545G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506564 | |||||||
| chr3:134506753 | C | G | 1 | a0001c0003t0003g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.45-356C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506753 | |||||||
| chr3:134506843 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.45-266G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506843 | |||||||
| chr3:134506873 | A | G | 262 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(259): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.45-236A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134506873 | |||||||
| chr3:134506918 | C | CA | 36 | a0001c0001t0001g0142 a0001c0001t0001g0286 a0001c0001t0001g0309 others(33): Show |
36 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.45-166dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134506918 | ||||||
| chr3:134506918 | CA | C | 20 | a0001c0001t0002g0076 a0001c0001t0004g0001 a0001c0001t0004g0039 others(17): Show |
22 | HG01069.hp2 HG01109.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.45-166delA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134506918 | ||||||
| chr3:134506918 | CAA | C | 10 | a0001c0001t0004g0089 a0001c0001t0005g0120 a0001c0001t0005g0125 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-167_45-166delAA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 134506918 | ||||||
| chr3:134507063 | C | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45-46C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 2/14 | chr3 | 134507063 | |||||||
| chr3:134507317 | C | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.222+31C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134507317 | |||||||
| chr3:134507636 | C | T | 2 | a0001c0001t0002g0067 a0001c0001t0002g0071 |
2 | NA18939.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.222+350C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134507636 | |||||||
| chr3:134507991 | G | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+705G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134507991 | |||||||
| chr3:134508074 | A | C | 1 | a0001c0001t0002g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.222+788A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508074 | |||||||
| chr3:134508258 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+972G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508258 | |||||||
| chr3:134508260 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.222+974G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508260 | |||||||
| chr3:134508410 | C | A | 7 | a0001c0003t0003g0170 a0001c0003t0003g0171 a0001c0003t0003g0172 others(4): Show |
7 | HG00280.hp1 HG01069.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+1124C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508410 | |||||||
| chr3:134508450 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+1164A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508450 | |||||||
| chr3:134508464 | G | T | 7 | a0001c0003t0003g0170 a0001c0003t0003g0171 a0001c0003t0003g0172 others(4): Show |
7 | HG00280.hp1 HG01069.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+1178G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508464 | |||||||
| chr3:134508667 | C | T | 1 | a0001c0003t0003g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.222+1381C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508667 | |||||||
| chr3:134508802 | C | A | 1 | a0001c0003t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+1516C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134508802 | |||||||
| chr3:134508971 | C | CT | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+1698dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134508971 | ||||||
| chr3:134509101 | G | T | 1 | a0001c0001t0004g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+1815G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509101 | |||||||
| chr3:134509196 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.222+1910G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509196 | |||||||
| chr3:134509340 | C | G | 16 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0021 others(13): Show |
16 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.222+2054C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509340 | |||||||
| chr3:134509357 | G | A | 1 | a0001c0001t0006g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+2071G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509357 | |||||||
| chr3:134509477 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.222+2191A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509477 | |||||||
| chr3:134509691 | C | A | 4 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0099 others(1): Show |
4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+2405C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509691 | |||||||
| chr3:134509786 | A | G | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.222+2500A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509786 | |||||||
| chr3:134509787 | A | G | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.222+2501A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509787 | |||||||
| chr3:134509934 | G | A | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+2648G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134509934 | |||||||
| chr3:134510131 | T | C | 1 | a0001c0001t0004g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.222+2845T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510131 | |||||||
| chr3:134510187 | T | C | 11 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
11 | HG01169.hp1 HG02630.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+2901T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510187 | |||||||
| chr3:134510253 | G | A | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+2967G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510253 | |||||||
| chr3:134510375 | A | G | 5 | a0001c0003t0001g0006 a0001c0003t0001g0150 a0001c0003t0001g0151 others(2): Show |
6 | HG00741.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+3089A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510375 | |||||||
| chr3:134510400 | G | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.222+3114G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510400 | |||||||
| chr3:134510563 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.222+3277G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510563 | |||||||
| chr3:134510570 | C | T | 1 | a0001c0003t0003g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.222+3284C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510570 | |||||||
| chr3:134510701 | G | A | 3 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0020g0092 |
3 | HG01884.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.222+3415G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510701 | |||||||
| chr3:134510794 | C | CTGG | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+3509_222+3511d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134510794 | ||||||
| chr3:134510830 | G | T | 1 | a0001c0001t0002g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.222+3544G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510830 | |||||||
| chr3:134510898 | C | G | 2 | a0002c0002t0001g0233 a0002c0002t0001g0234 |
2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.222+3612C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510898 | |||||||
| chr3:134510898 | C | T | 2 | a0001c0001t0013g0087 a0001c0001t0013g0088 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.222+3612C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134510898 | |||||||
| chr3:134510973 | A | AT | 209 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(206): Show |
214 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.222+3699dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134510973 | ||||||
| chr3:134511024 | C | G | 220 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(217): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.222+3738C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511024 | |||||||
| chr3:134511172 | A | G | 2 | a0002c0002t0001g0212 a0002c0002t0001g0267 |
2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.222+3886A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511172 | |||||||
| chr3:134511324 | T | C | 1 | a0002c0002t0001g0274 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.222+4038T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511324 | |||||||
| chr3:134511362 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.222+4076T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511362 | |||||||
| chr3:134511392 | A | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+4106A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511392 | |||||||
| chr3:134511535 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.222+4249C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511535 | |||||||
| chr3:134511604 | C | T | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+4318C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511604 | |||||||
| chr3:134511662 | T | C | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+4376T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511662 | |||||||
| chr3:134511704 | G | C | 1 | a0001c0001t0002g0009 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.222+4418G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511704 | |||||||
| chr3:134511861 | A | G | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.222+4575A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511861 | |||||||
| chr3:134511969 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+4683A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134511969 | |||||||
| chr3:134512152 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.222+4866C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512152 | |||||||
| chr3:134512164 | A | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.222+4878A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512164 | |||||||
| chr3:134512215 | CTG | C | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+4932_222+4933d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134512215 | ||||||
| chr3:134512223 | A | G | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.222+4937A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512223 | |||||||
| chr3:134512409 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.222+5123T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512409 | |||||||
| chr3:134512606 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.222+5320C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512606 | |||||||
| chr3:134512689 | A | G | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+5403A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134512689 | |||||||
| chr3:134513088 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.222+5802C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513088 | |||||||
| chr3:134513281 | A | G | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+5995A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513281 | |||||||
| chr3:134513373 | C | T | 2 | a0001c0001t0002g0101 a0001c0001t0020g0092 |
2 | HG03654.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.222+6087C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513373 | |||||||
| chr3:134513412 | T | C | 2 | a0002c0002t0001g0282 a0002c0002t0001g0292 |
2 | HG01516.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.222+6126T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513412 | |||||||
| chr3:134513486 | A | T | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.222+6200A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513486 | |||||||
| chr3:134513497 | A | G | 84 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(81): Show |
86 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.222+6211A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513497 | |||||||
| chr3:134513508 | A | G | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(87): Show |
95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.222+6222A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513508 | |||||||
| chr3:134513554 | C | A | 308 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.222+6268C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513554 | |||||||
| chr3:134513586 | CATT | C | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+6305_222+6307d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134513586 | ||||||
| chr3:134513624 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+6338A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513624 | |||||||
| chr3:134513735 | G | A | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.222+6449G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513735 | |||||||
| chr3:134513805 | A | G | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+6519A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513805 | |||||||
| chr3:134513825 | A | G | 1 | a0006c0012t0016g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.222+6539A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513825 | |||||||
| chr3:134513998 | C | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+6712C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134513998 | |||||||
| chr3:134514078 | C | G | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.222+6792C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514078 | |||||||
| chr3:134514146 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.222+6860G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514146 | |||||||
| chr3:134514250 | A | G | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.222+6964A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514250 | |||||||
| chr3:134514307 | A | G | 1 | a0001c0001t0014g0033 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.222+7021A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514307 | |||||||
| chr3:134514396 | G | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.222+7110G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514396 | |||||||
| chr3:134514569 | T | C | 1 | a0001c0001t0006g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.222+7283T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514569 | |||||||
| chr3:134514623 | GA | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+7341delA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134514623 | ||||||
| chr3:134514752 | C | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+7466C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134514752 | |||||||
| chr3:134515503 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+8217C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134515503 | |||||||
| chr3:134515514 | C | T | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.222+8228C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134515514 | |||||||
| chr3:134515543 | G | A | 2 | a0001c0003t0027g0163 a0001c0003t0028g0164 |
2 | HG00735.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.222+8257G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134515543 | |||||||
| chr3:134515994 | G | A | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.222+8708G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134515994 | |||||||
| chr3:134516129 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+8843C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516129 | |||||||
| chr3:134516279 | A | G | 1 | a0002c0002t0001g0273 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.222+8993A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516279 | |||||||
| chr3:134516319 | G | A | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.222+9033G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516319 | |||||||
| chr3:134516323 | T | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+9037T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516323 | |||||||
| chr3:134516476 | C | A | 1 | a0002c0002t0001g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.222+9190C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516476 | |||||||
| chr3:134516503 | G | A | 8 | a0001c0003t0001g0006 a0001c0003t0001g0141 a0001c0003t0001g0146 others(5): Show |
9 | HG00741.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+9217G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516503 | |||||||
| chr3:134516749 | C | T | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.222+9463C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516749 | |||||||
| chr3:134516750 | A | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0286 others(11): Show |
15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.222+9464A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516750 | |||||||
| chr3:134516762 | A | C | 12 | a0001c0001t0001g0211 a0001c0001t0001g0221 a0001c0001t0001g0263 others(9): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.222+9476A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516762 | |||||||
| chr3:134516884 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.222+9598C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516884 | |||||||
| chr3:134516948 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+9662A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134516948 | |||||||
| chr3:134517128 | G | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.222+9842G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517128 | |||||||
| chr3:134517233 | C | G | 1 | a0001c0001t0004g0044 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.222+9947C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517233 | |||||||
| chr3:134517464 | C | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.222+10178C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517464 | |||||||
| chr3:134517602 | C | T | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.222+10316C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517602 | |||||||
| chr3:134517607 | C | T | 80 | a0002c0002t0001g0002 a0002c0002t0001g0103 a0002c0002t0001g0209 others(77): Show |
82 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.222+10321C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517607 | |||||||
| chr3:134517617 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.222+10331G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134517617 | |||||||
| chr3:134518230 | A | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+10944A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518230 | |||||||
| chr3:134518261 | C | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.222+10975C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518261 | |||||||
| chr3:134518354 | A | G | 303 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.222+11068A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518354 | |||||||
| chr3:134518395 | C | T | 1 | a0001c0003t0003g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.222+11109C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518395 | |||||||
| chr3:134518430 | A | C | 303 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.222+11144A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518430 | |||||||
| chr3:134518871 | C | T | 1 | a0001c0001t0004g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.222+11585C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518871 | |||||||
| chr3:134518875 | A | C | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+11589A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518875 | |||||||
| chr3:134518915 | G | GA | 5 | a0001c0001t0004g0044 a0001c0001t0012g0105 a0001c0001t0012g0106 others(2): Show |
5 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+11635dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134518915 | ||||||
| chr3:134518937 | A | C | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+11651A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134518937 | |||||||
| chr3:134519024 | A | AC | 11 | a0001c0001t0002g0058 a0001c0001t0004g0044 a0001c0001t0005g0120 others(8): Show |
11 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.222+11745dupC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134519024 | ||||||
| chr3:134519158 | C | T | 1 | a0002c0002t0001g0103 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.222+11872C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519158 | |||||||
| chr3:134519381 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(3): Show |
6 | HG00738.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+12095G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519381 | |||||||
| chr3:134519392 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.222+12106C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519392 | |||||||
| chr3:134519425 | C | T | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+12139C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519425 | |||||||
| chr3:134519430 | G | A | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.222+12144G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519430 | |||||||
| chr3:134519431 | G | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.222+12145G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519431 | |||||||
| chr3:134519434 | G | A | 2 | a0002c0002t0001g0241 a0002c0002t0001g0293 |
2 | NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.222+12148G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519434 | |||||||
| chr3:134519499 | G | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.222+12213G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519499 | |||||||
| chr3:134519564 | A | T | 1 | a0001c0001t0004g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+12278A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519564 | |||||||
| chr3:134519911 | T | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.223-11934T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134519911 | |||||||
| chr3:134520017 | G | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-11828G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520017 | |||||||
| chr3:134520062 | T | G | 1 | a0001c0001t0002g0069 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.223-11783T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520062 | |||||||
| chr3:134520122 | A | C | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.223-11723A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520122 | |||||||
| chr3:134520186 | C | T | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.223-11659C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520186 | |||||||
| chr3:134520293 | A | T | 1 | a0001c0001t0018g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.223-11552A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520293 | |||||||
| chr3:134520349 | T | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.223-11496T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520349 | |||||||
| chr3:134520559 | C | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0062 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.223-11286C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520559 | |||||||
| chr3:134520594 | G | C | 1 | a0002c0002t0001g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.223-11251G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520594 | |||||||
| chr3:134520675 | A | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.223-11170A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520675 | |||||||
| chr3:134520702 | G | T | 2 | a0001c0001t0014g0032 a0001c0001t0014g0033 |
2 | HG01106.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.223-11143G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520702 | |||||||
| chr3:134520734 | A | G | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-11111A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520734 | |||||||
| chr3:134520760 | T | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-11085T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520760 | |||||||
| chr3:134520926 | A | G | 5 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0168 others(2): Show |
5 | HG00733.hp1 HG01123.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-10919A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134520926 | |||||||
| chr3:134521446 | TC | T | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.223-10394delC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134521446 | ||||||
| chr3:134521451 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.223-10394C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521451 | |||||||
| chr3:134521572 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-10273C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521572 | |||||||
| chr3:134521707 | C | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223-10138C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521707 | |||||||
| chr3:134521777 | C | T | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-10068C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521777 | |||||||
| chr3:134521792 | A | C | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.223-10053A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521792 | |||||||
| chr3:134521928 | G | C | 2 | a0002c0002t0001g0242 a0002c0002t0001g0243 |
2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.223-9917G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134521928 | |||||||
| chr3:134522397 | TGAAA | T | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.223-9444_223-9441d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134522397 | ||||||
| chr3:134522468 | A | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.223-9377A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522468 | |||||||
| chr3:134522535 | G | A | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-9310G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522535 | |||||||
| chr3:134522726 | T | A | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.223-9119T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522726 | |||||||
| chr3:134522865 | C | T | 1 | a0002c0002t0001g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.223-8980C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522865 | |||||||
| chr3:134522986 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0062 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.223-8859C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134522986 | |||||||
| chr3:134523030 | C | T | 1 | a0001c0003t0003g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.223-8815C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523030 | |||||||
| chr3:134523060 | T | C | 1 | a0001c0003t0003g0168 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.223-8785T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523060 | |||||||
| chr3:134523179 | T | G | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(87): Show |
95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.223-8666T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523179 | |||||||
| chr3:134523209 | T | A | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.223-8636T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523209 | |||||||
| chr3:134523292 | G | A | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.223-8553G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523292 | |||||||
| chr3:134523314 | C | T | 5 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(2): Show |
5 | HG01109.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-8531C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523314 | |||||||
| chr3:134523341 | C | A | 2 | a0001c0003t0003g0185 a0001c0003t0023g0173 |
2 | HG02071.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.223-8504C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523341 | |||||||
| chr3:134523460 | G | T | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-8385G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523460 | |||||||
| chr3:134523543 | A | G | 2 | a0001c0001t0002g0029 a0001c0001t0018g0030 |
2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.223-8302A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523543 | |||||||
| chr3:134523594 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.223-8251A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523594 | |||||||
| chr3:134523677 | T | C | 1 | a0002c0002t0001g0308 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.223-8168T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523677 | |||||||
| chr3:134523756 | T | C | 4 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0099 others(1): Show |
4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-8089T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523756 | |||||||
| chr3:134523821 | G | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223-8024G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523821 | |||||||
| chr3:134523982 | G | A | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.223-7863G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523982 | |||||||
| chr3:134523996 | A | G | 2 | a0001c0001t0007g0116 a0001c0001t0007g0117 |
2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.223-7849A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134523996 | |||||||
| chr3:134524033 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.223-7812T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524033 | |||||||
| chr3:134524116 | A | G | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.223-7729A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524116 | |||||||
| chr3:134524247 | C | G | 9 | a0002c0002t0001g0226 a0002c0002t0001g0237 a0002c0002t0001g0240 others(6): Show |
9 | HG01081.hp2 HG01346.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-7598C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524247 | |||||||
| chr3:134524505 | T | C | 11 | a0001c0001t0002g0074 a0001c0001t0002g0083 a0001c0001t0002g0084 others(8): Show |
12 | HG00140.hp2 HG01099.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.223-7340T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524505 | |||||||
| chr3:134524522 | A | G | 1 | a0001c0003t0003g0194 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.223-7323A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524522 | |||||||
| chr3:134524623 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-7222C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524623 | |||||||
| chr3:134524702 | G | A | 1 | a0001c0003t0003g0184 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.223-7143G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524702 | |||||||
| chr3:134524965 | C | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
5 | NA18972.hp1 NA18981.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-6880C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134524965 | |||||||
| chr3:134525009 | C | T | 1 | a0001c0001t0021g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223-6836C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525009 | |||||||
| chr3:134525072 | C | T | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-6773C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525072 | |||||||
| chr3:134525127 | C | T | 1 | a0007c0008t0003g0182 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.223-6718C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525127 | |||||||
| chr3:134525193 | C | T | 4 | a0002c0002t0001g0218 a0002c0002t0001g0259 a0002c0002t0001g0275 others(1): Show |
4 | HG00609.hp1 NA18940.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-6652C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525193 | |||||||
| chr3:134525313 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-6532G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525313 | |||||||
| chr3:134525410 | A | G | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.223-6435A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525410 | |||||||
| chr3:134525548 | T | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-6297T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525548 | |||||||
| chr3:134525717 | G | A | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.223-6128G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525717 | |||||||
| chr3:134525858 | C | T | 4 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0099 others(1): Show |
4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-5987C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525858 | |||||||
| chr3:134525882 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.223-5963C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134525882 | |||||||
| chr3:134526117 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.223-5728G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526117 | |||||||
| chr3:134526149 | C | T | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.223-5696C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526149 | |||||||
| chr3:134526259 | G | A | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.223-5586G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526259 | |||||||
| chr3:134526272 | G | C | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223-5573G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526272 | |||||||
| chr3:134526318 | T | A | 81 | a0001c0001t0001g0008 a0002c0002t0001g0002 a0002c0002t0001g0103 others(78): Show |
84 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.223-5527T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526318 | |||||||
| chr3:134526434 | C | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223-5411C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526434 | |||||||
| chr3:134526459 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.223-5386C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526459 | |||||||
| chr3:134526486 | C | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG01496.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.223-5359C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526486 | |||||||
| chr3:134526536 | G | A | 1 | a0001c0003t0003g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.223-5309G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526536 | |||||||
| chr3:134526592 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.223-5253T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526592 | |||||||
| chr3:134526609 | C | G | 5 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(2): Show |
5 | NA18941.hp2 NA18955.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-5236C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526609 | |||||||
| chr3:134526663 | G | A | 12 | a0001c0001t0001g0211 a0001c0001t0001g0221 a0001c0001t0001g0263 others(9): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.223-5182G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526663 | |||||||
| chr3:134526870 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.223-4975G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526870 | |||||||
| chr3:134526917 | TG | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-4921delG | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134526917 | ||||||
| chr3:134526921 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.223-4924G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526921 | |||||||
| chr3:134526954 | G | T | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-4891G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134526954 | |||||||
| chr3:134527024 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-4821A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527024 | |||||||
| chr3:134527087 | T | C | 11 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(8): Show |
11 | HG01109.hp2 HG01123.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-4758T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527087 | |||||||
| chr3:134527217 | G | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.223-4628G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527217 | |||||||
| chr3:134527252 | A | T | 1 | a0002c0002t0001g0243 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.223-4593A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527252 | |||||||
| chr3:134527870 | A | AGTTCGGG others(15): Show |
2 | a0001c0003t0003g0165 a0007c0008t0003g0182 |
2 | HG02015.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.223-3974_223-3953d others(24): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134527870 | ||||||
| chr3:134527966 | T | A | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.223-3879T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527966 | |||||||
| chr3:134527967 | C | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-3878C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134527967 | |||||||
| chr3:134528361 | C | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-3484C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528361 | |||||||
| chr3:134528389 | T | C | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.223-3456T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528389 | |||||||
| chr3:134528565 | T | TGC | 19 | a0001c0001t0002g0017 a0001c0001t0002g0059 a0001c0001t0002g0064 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.223-3279_223-3278i others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528565 | ||||||
| chr3:134528567 | T | C | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(66): Show |
74 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.223-3278T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528567 | |||||||
| chr3:134528569 | C | CGT | 9 | a0001c0001t0006g0005 a0001c0001t0006g0072 a0001c0001t0006g0073 others(6): Show |
10 | HG01175.hp1 HG01261.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-3252_223-3251d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGT | 5 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-3254_223-3251d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGTGT | 68 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(65): Show |
70 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.223-3256_223-3251d others(8): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGTGTA others(7): Show |
1 | a0001c0001t0009g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.223-3270_223-3269i others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGTGTG others(1): Show |
20 | a0001c0001t0001g0149 a0001c0001t0001g0206 a0001c0001t0001g0207 others(17): Show |
20 | HG00140.hp1 HG01109.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.223-3258_223-3251d others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGTGTG others(3): Show |
88 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0286 others(85): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.223-3260_223-3251d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGTGTG others(5): Show |
13 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(10): Show |
13 | HG01081.hp2 HG01496.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.223-3262_223-3251d others(14): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGTGTG others(7): Show |
7 | a0001c0001t0001g0211 a0001c0001t0005g0122 a0001c0001t0009g0097 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-3264_223-3251d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGTGTG others(9): Show |
6 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0123 others(3): Show |
6 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.223-3266_223-3251d others(18): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | CGTGTGTG others(11): Show |
4 | a0001c0001t0005g0124 a0001c0001t0005g0127 a0001c0001t0025g0119 others(1): Show |
4 | HG02818.hp1 HG03540.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-3268_223-3251d others(20): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134528569 | ||||||
| chr3:134528569 | C | T | 84 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(81): Show |
88 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.223-3276C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528569 | |||||||
| chr3:134528594 | G | GTGTGTGT others(4): Show |
1 | a0002c0002t0001g0262 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.223-3251_223-3250i others(13): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528594 | |||||||
| chr3:134528759 | G | A | 23 | a0001c0001t0004g0001 a0001c0001t0004g0019 a0001c0001t0004g0020 others(20): Show |
25 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.223-3086G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528759 | |||||||
| chr3:134528864 | A | C | 26 | a0001c0001t0002g0017 a0001c0001t0002g0064 a0001c0001t0002g0065 others(23): Show |
27 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.223-2981A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134528864 | |||||||
| chr3:134529021 | C | A | 303 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.223-2824C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529021 | |||||||
| chr3:134529026 | A | G | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.223-2819A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529026 | |||||||
| chr3:134529168 | G | C | 303 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.223-2677G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529168 | |||||||
| chr3:134529185 | G | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-2660G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529185 | |||||||
| chr3:134529339 | C | CT | 96 | a0001c0001t0001g0305 a0001c0001t0002g0003 a0001c0001t0002g0004 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.223-2487dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529339 | ||||||
| chr3:134529339 | C | CTT | 188 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(185): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.223-2488_223-2487d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529339 | ||||||
| chr3:134529339 | C | CTTT | 7 | a0001c0001t0001g0139 a0001c0001t0001g0300 a0001c0001t0021g0108 others(4): Show |
7 | HG01099.hp2 HG02071.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2489_223-2487d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529339 | ||||||
| chr3:134529444 | G | A | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2401G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529444 | |||||||
| chr3:134529576 | A | G | 2 | a0001c0001t0015g0144 a0001c0001t0015g0145 |
2 | HG01169.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.223-2269A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529576 | |||||||
| chr3:134529604 | G | A | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.223-2241G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529604 | |||||||
| chr3:134529672 | C | A | 1 | a0002c0002t0001g0223 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.223-2173C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529672 | |||||||
| chr3:134529868 | A | AT | 228 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(225): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.223-1953dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529868 | ||||||
| chr3:134529868 | A | ATT | 44 | a0001c0001t0001g0008 a0001c0001t0001g0206 a0001c0001t0001g0207 others(41): Show |
45 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.223-1954_223-1953d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529868 | ||||||
| chr3:134529868 | A | ATTT | 11 | a0001c0001t0001g0208 a0001c0001t0001g0300 a0001c0001t0002g0028 others(8): Show |
11 | HG01891.hp1 HG03540.hp2 HG04115.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-1955_223-1953d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 134529868 | ||||||
| chr3:134529959 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-1886C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134529959 | |||||||
| chr3:134530027 | C | T | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.223-1818C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530027 | |||||||
| chr3:134530064 | G | T | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-1781G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530064 | |||||||
| chr3:134530118 | C | T | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.223-1727C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530118 | |||||||
| chr3:134530162 | C | T | 1 | a0001c0003t0001g0134 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.223-1683C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530162 | |||||||
| chr3:134530209 | C | T | 1 | a0001c0001t0005g0126 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.223-1636C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530209 | |||||||
| chr3:134530505 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.223-1340T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530505 | |||||||
| chr3:134530574 | T | C | 1 | a0001c0001t0002g0084 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.223-1271T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530574 | |||||||
| chr3:134530829 | T | C | 1 | a0002c0002t0001g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.223-1016T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530829 | |||||||
| chr3:134530927 | C | G | 194 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(191): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.223-918C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530927 | |||||||
| chr3:134530946 | C | T | 5 | a0002c0002t0001g0218 a0002c0002t0001g0259 a0002c0002t0001g0275 others(2): Show |
5 | HG00609.hp1 NA18940.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-899C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530946 | |||||||
| chr3:134530970 | G | A | 1 | a0008c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.223-875G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134530970 | |||||||
| chr3:134531057 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-788A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531057 | |||||||
| chr3:134531072 | C | T | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-773C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531072 | |||||||
| chr3:134531129 | G | A | 5 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(2): Show |
5 | NA18939.hp2 NA18999.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-716G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531129 | |||||||
| chr3:134531257 | G | T | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(87): Show |
95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.223-588G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531257 | |||||||
| chr3:134531294 | C | G | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 |
3 | HG00280.hp2 HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.223-551C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531294 | |||||||
| chr3:134531483 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.223-362C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531483 | |||||||
| chr3:134531553 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0289 a0001c0010t0001g0290 |
3 | HG00323.hp2 HG02300.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.223-292G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531553 | |||||||
| chr3:134531734 | T | C | 1 | a0001c0001t0021g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223-111T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531734 | |||||||
| chr3:134531766 | G | T | 1 | a0001c0003t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.223-79G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 3/14 | chr3 | 134531766 | |||||||
| chr3:134531969 | G | A | 8 | a0001c0001t0005g0120 a0001c0001t0005g0122 a0001c0001t0005g0123 others(5): Show |
8 | NA18940.hp2 NA18951.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+29G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134531969 | |||||||
| chr3:134532053 | A | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+113A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532053 | |||||||
| chr3:134532197 | A | G | 308 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.318+257A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532197 | |||||||
| chr3:134532326 | A | C | 1 | a0001c0001t0001g0287 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.318+386A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532326 | |||||||
| chr3:134532342 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.318+402A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532342 | |||||||
| chr3:134532540 | T | G | 13 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(10): Show |
13 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.319-238T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532540 | |||||||
| chr3:134532564 | A | T | 1 | a0002c0002t0001g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-214A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532564 | |||||||
| chr3:134532573 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.319-205A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532573 | |||||||
| chr3:134532634 | T | C | 1 | a0001c0001t0011g0110 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.319-144T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 4/14 | chr3 | 134532634 | |||||||
| chr3:134533017 | A | G | 1 | a0001c0003t0003g0179 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.441+117A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533017 | |||||||
| chr3:134533052 | C | T | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+152C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533052 | |||||||
| chr3:134533272 | C | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.441+372C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533272 | |||||||
| chr3:134533292 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.441+392A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533292 | |||||||
| chr3:134533372 | C | T | 1 | a0002c0002t0001g0242 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.441+472C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533372 | |||||||
| chr3:134533508 | A | G | 1 | a0001c0001t0024g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.441+608A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533508 | |||||||
| chr3:134533543 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.441+643T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533543 | |||||||
| chr3:134533611 | C | G | 1 | a0001c0001t0004g0019 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.441+711C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533611 | |||||||
| chr3:134533620 | C | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.441+720C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533620 | |||||||
| chr3:134533649 | G | T | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.441+749G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134533649 | |||||||
| chr3:134534412 | A | G | 2 | a0002c0002t0001g0254 a0002c0002t0001g0274 |
2 | HG00423.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.441+1512A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134534412 | |||||||
| chr3:134534755 | T | C | 13 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(10): Show |
13 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+1855T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134534755 | |||||||
| chr3:134534803 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0286 others(11): Show |
15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+1903A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134534803 | |||||||
| chr3:134534889 | T | C | 2 | a0002c0002t0001g0238 a0002c0002t0001g0245 |
2 | HG01884.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.441+1989T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134534889 | |||||||
| chr3:134535079 | A | G | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-2076A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535079 | |||||||
| chr3:134535209 | G | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1946G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535209 | |||||||
| chr3:134535340 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.442-1815C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535340 | |||||||
| chr3:134535495 | C | CT | 185 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(182): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.442-1657dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 134535495 | ||||||
| chr3:134535495 | C | CTT | 5 | a0001c0003t0001g0153 a0001c0003t0003g0170 a0001c0003t0003g0171 others(2): Show |
5 | HG00280.hp1 HG01106.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-1658_442-1657d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 134535495 | ||||||
| chr3:134535498 | TC | T | 91 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(88): Show |
96 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.442-1655delC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 134535498 | ||||||
| chr3:134535499 | C | T | 216 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(213): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.442-1656C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535499 | |||||||
| chr3:134535500 | C | T | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.442-1655C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535500 | |||||||
| chr3:134535665 | A | T | 1 | a0001c0003t0003g0161 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.442-1490A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535665 | |||||||
| chr3:134535788 | G | A | 1 | a0001c0001t0013g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442-1367G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535788 | |||||||
| chr3:134535870 | A | G | 6 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | NA18939.hp2 NA18999.hp2 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-1285A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134535870 | |||||||
| chr3:134536062 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442-1093C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536062 | |||||||
| chr3:134536147 | C | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.442-1008C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536147 | |||||||
| chr3:134536149 | A | G | 197 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(194): Show |
202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.442-1006A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536149 | |||||||
| chr3:134536153 | C | G | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(87): Show |
95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.442-1002C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536153 | |||||||
| chr3:134536189 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442-966C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536189 | |||||||
| chr3:134536300 | A | T | 1 | a0002c0002t0001g0278 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.442-855A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536300 | |||||||
| chr3:134536410 | G | C | 3 | a0001c0001t0007g0115 a0001c0001t0007g0116 a0001c0001t0007g0117 |
3 | HG02572.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-745G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536410 | |||||||
| chr3:134536457 | C | T | 4 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-698C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536457 | |||||||
| chr3:134536834 | A | T | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.442-321A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536834 | |||||||
| chr3:134536909 | T | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-246T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536909 | |||||||
| chr3:134536912 | G | T | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-243G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134536912 | |||||||
| chr3:134537091 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.442-64G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 5/14 | chr3 | 134537091 | |||||||
| chr3:134537317 | A | G | 96 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0286 others(93): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.555+49A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537317 | |||||||
| chr3:134537378 | C | T | 8 | a0002c0002t0001g0236 a0002c0002t0001g0239 a0002c0002t0001g0242 others(5): Show |
8 | HG01981.hp1 HG02698.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.555+110C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537378 | |||||||
| chr3:134537404 | C | T | 1 | a0001c0001t0005g0126 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.555+136C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537404 | |||||||
| chr3:134537628 | C | T | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.555+360C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537628 | |||||||
| chr3:134537658 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.555+390C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537658 | |||||||
| chr3:134537789 | G | A | 1 | a0001c0003t0003g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.555+521G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134537789 | |||||||
| chr3:134538058 | G | A | 3 | a0001c0001t0004g0094 a0001c0001t0004g0095 a0001c0001t0004g0096 |
3 | HG00099.hp1 HG02683.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.555+790G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538058 | |||||||
| chr3:134538198 | G | GT | 7 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0054 others(4): Show |
7 | HG00140.hp2 HG01175.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+950dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | ||||||
| chr3:134538198 | G | GTTT | 8 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(5): Show |
8 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.555+948_555+950dup others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | ||||||
| chr3:134538198 | GT | G | 29 | a0001c0001t0001g0221 a0001c0001t0001g0266 a0001c0001t0001g0286 others(26): Show |
29 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.555+950delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | ||||||
| chr3:134538198 | GTT | G | 161 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(158): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.555+949_555+950del others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | ||||||
| chr3:134538198 | GTTT | G | 10 | a0001c0001t0001g0131 a0001c0003t0001g0006 a0001c0003t0001g0140 others(7): Show |
11 | HG00741.hp1 HG02895.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+948_555+950del others(3): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538198 | ||||||
| chr3:134538328 | C | T | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.555+1060C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538328 | |||||||
| chr3:134538372 | G | T | 4 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0099 others(1): Show |
4 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+1104G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538372 | |||||||
| chr3:134538397 | A | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+1129A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538397 | |||||||
| chr3:134538474 | G | GT | 8 | a0001c0003t0003g0191 a0001c0003t0003g0196 a0001c0003t0003g0200 others(5): Show |
8 | HG00423.hp1 HG02523.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.555+1213dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538474 | ||||||
| chr3:134538517 | G | T | 2 | a0001c0001t0009g0097 a0001c0001t0009g0098 |
2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.555+1249G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538517 | |||||||
| chr3:134538529 | G | GTGTATAT others(25): Show |
1 | a0002c0002t0001g0292 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(34): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538529 | ||||||
| chr3:134538529 | G | GTGTATAT others(27): Show |
1 | a0002c0002t0001g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(36): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538529 | ||||||
| chr3:134538531 | G | GTA | 67 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0016 others(64): Show |
70 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATA | 91 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(88): Show |
93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATA | 42 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0149 others(39): Show |
45 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(8): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0299 a0001c0001t0002g0060 a0001c0001t0002g0104 others(4): Show |
7 | HG00609.hp2 HG01255.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(10): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(3): Show |
2 | a0001c0001t0009g0097 a0001c0003t0003g0204 |
2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(15): Show |
1 | a0002c0002t0001g0223 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(24): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(33): Show |
2 | a0002c0002t0001g0238 a0002c0002t0001g0243 |
2 | HG01884.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(42): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(35): Show |
3 | a0002c0002t0001g0239 a0002c0002t0001g0245 a0002c0002t0001g0252 |
3 | HG01981.hp1 NA18969.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(44): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(31): Show |
2 | a0002c0002t0001g0242 a0002c0002t0001g0280 |
2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(40): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(29): Show |
9 | a0002c0002t0001g0214 a0002c0002t0001g0241 a0002c0002t0001g0253 others(6): Show |
9 | HG00735.hp1 HG01099.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(38): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(31): Show |
1 | a0002c0002t0001g0258 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(40): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(25): Show |
1 | a0002c0002t0001g0282 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(34): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(27): Show |
1 | a0002c0002t0001g0256 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(36): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(55): Show |
2 | a0002c0002t0001g0212 a0002c0002t0001g0267 |
2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(64): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(23): Show |
2 | a0002c0002t0001g0233 a0002c0002t0001g0234 |
2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(32): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(25): Show |
31 | a0002c0002t0001g0002 a0002c0002t0001g0209 a0002c0002t0001g0215 others(28): Show |
33 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(34): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(27): Show |
13 | a0002c0002t0001g0224 a0002c0002t0001g0225 a0002c0002t0001g0244 others(10): Show |
13 | HG00544.hp1 HG00609.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.555+1264_555+1265i others(36): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(29): Show |
3 | a0002c0002t0001g0268 a0002c0002t0001g0298 a0002c0002t0022g0246 |
3 | HG01258.hp1 HG02015.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.555+1264_555+1265i others(38): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(33): Show |
1 | a0002c0002t0001g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(42): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(55): Show |
1 | a0002c0002t0001g0303 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.555+1264_555+1265i others(64): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538531 | G | GTATATAT others(27): Show |
1 | a0002c0002t0001g0251 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.555+1264_555+1265i others(36): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538531 | ||||||
| chr3:134538533 | G | A | 289 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(286): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.555+1265G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538533 | |||||||
| chr3:134538533 | G | GTA | 4 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+1285_555+1286d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538533 | ||||||
| chr3:134538533 | G | GTATA | 9 | a0001c0001t0001g0211 a0001c0001t0001g0221 a0001c0001t0001g0263 others(6): Show |
9 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+1283_555+1286d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134538533 | ||||||
| chr3:134538567 | T | A | 1 | a0001c0001t0005g0122 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.555+1299T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538567 | |||||||
| chr3:134538698 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.555+1430G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134538698 | |||||||
| chr3:134539275 | A | ATT | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+2011_555+2012d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134539275 | ||||||
| chr3:134539452 | T | A | 3 | a0001c0001t0006g0005 a0001c0001t0006g0072 a0001c0001t0006g0080 |
4 | HG01346.hp1 HG01981.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+2184T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134539452 | |||||||
| chr3:134539692 | T | TA | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+2433dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134539692 | ||||||
| chr3:134539863 | A | C | 2 | a0001c0003t0001g0134 a0001c0003t0001g0140 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.555+2595A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134539863 | |||||||
| chr3:134540004 | C | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+2736C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540004 | |||||||
| chr3:134540284 | T | G | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.555+3016T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540284 | |||||||
| chr3:134540361 | C | T | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.555+3093C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540361 | |||||||
| chr3:134540604 | T | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.555+3336T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540604 | |||||||
| chr3:134540764 | A | AT | 242 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(239): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.555+3514dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134540764 | ||||||
| chr3:134540764 | A | ATT | 7 | a0001c0001t0001g0286 a0001c0001t0005g0121 a0001c0001t0024g0113 others(4): Show |
7 | HG02056.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+3513_555+3514d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134540764 | ||||||
| chr3:134540783 | A | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.555+3515A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540783 | |||||||
| chr3:134540811 | T | C | 20 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(17): Show |
20 | HG01109.hp2 HG01123.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.555+3543T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540811 | |||||||
| chr3:134540938 | C | T | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.555+3670C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540938 | |||||||
| chr3:134540969 | A | T | 1 | a0001c0001t0024g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.555+3701A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134540969 | |||||||
| chr3:134541061 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.555+3793C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541061 | |||||||
| chr3:134541112 | C | T | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(87): Show |
95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.555+3844C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541112 | |||||||
| chr3:134541145 | T | C | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.555+3877T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541145 | |||||||
| chr3:134541199 | C | G | 6 | a0001c0003t0003g0191 a0001c0003t0003g0196 a0001c0003t0003g0200 others(3): Show |
6 | HG00423.hp1 HG02523.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+3931C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541199 | |||||||
| chr3:134541510 | C | CT | 24 | a0001c0001t0001g0265 a0001c0001t0001g0286 a0001c0001t0001g0305 others(21): Show |
24 | HG00280.hp2 HG00738.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.556-4054dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134541510 | ||||||
| chr3:134541510 | CT | C | 7 | a0001c0001t0001g0139 a0001c0001t0002g0076 a0001c0001t0002g0077 others(4): Show |
7 | HG01069.hp2 HG01516.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-4054delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134541510 | ||||||
| chr3:134541602 | G | A | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.556-3984G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541602 | |||||||
| chr3:134541655 | A | C | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-3931A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541655 | |||||||
| chr3:134541658 | C | T | 1 | a0002c0002t0001g0311 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.556-3928C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541658 | |||||||
| chr3:134541733 | G | A | 1 | a0002c0002t0001g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.556-3853G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541733 | |||||||
| chr3:134541753 | TC | T | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(87): Show |
95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.556-3831delC | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134541753 | ||||||
| chr3:134541759 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.556-3827C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541759 | |||||||
| chr3:134541843 | G | T | 1 | a0001c0001t0004g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.556-3743G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541843 | |||||||
| chr3:134541873 | A | G | 1 | a0001c0001t0004g0295 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.556-3713A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541873 | |||||||
| chr3:134541921 | A | C | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.556-3665A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541921 | |||||||
| chr3:134541972 | A | C | 53 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 others(50): Show |
54 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.556-3614A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134541972 | |||||||
| chr3:134542018 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.556-3568G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542018 | |||||||
| chr3:134542023 | G | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0031 a0001c0001t0002g0041 |
3 | HG01243.hp2 HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.556-3563G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542023 | |||||||
| chr3:134542273 | T | A | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.556-3313T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542273 | |||||||
| chr3:134542281 | C | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.556-3305C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542281 | |||||||
| chr3:134542402 | C | A | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.556-3184C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542402 | |||||||
| chr3:134542403 | A | C | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.556-3183A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542403 | |||||||
| chr3:134542500 | G | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.556-3086G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542500 | |||||||
| chr3:134542595 | T | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.556-2991T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542595 | |||||||
| chr3:134542596 | T | C | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.556-2990T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542596 | |||||||
| chr3:134542705 | C | A | 1 | a0001c0001t0024g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.556-2881C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542705 | |||||||
| chr3:134542812 | C | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.556-2774C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134542812 | |||||||
| chr3:134542940 | C | CA | 99 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(96): Show |
104 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.556-2633dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134542940 | ||||||
| chr3:134542940 | C | CAA | 192 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(189): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.556-2634_556-2633d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134542940 | ||||||
| chr3:134542940 | C | CAAA | 13 | a0001c0001t0001g0142 a0001c0001t0005g0120 a0001c0001t0005g0121 others(10): Show |
13 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.556-2635_556-2633d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134542940 | ||||||
| chr3:134543248 | A | G | 7 | a0001c0001t0004g0042 a0001c0003t0003g0166 a0001c0003t0003g0167 others(4): Show |
7 | HG02056.hp1 HG02155.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.556-2338A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543248 | |||||||
| chr3:134543406 | T | A | 1 | a0001c0003t0003g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.556-2180T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543406 | |||||||
| chr3:134543779 | C | T | 1 | a0002c0002t0001g0239 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.556-1807C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543779 | |||||||
| chr3:134543845 | AG | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.556-1740delG | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543845 | |||||||
| chr3:134543846 | G | A | 117 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(114): Show |
122 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.556-1740G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134543846 | |||||||
| chr3:134543961 | T | TA | 7 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0010g0086 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.556-1612dupA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134543961 | ||||||
| chr3:134543961 | TA | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.556-1612delA | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134543961 | ||||||
| chr3:134544055 | C | G | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-1531C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544055 | |||||||
| chr3:134544151 | G | A | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.556-1435G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544151 | |||||||
| chr3:134544248 | C | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
5 | NA18972.hp1 NA18981.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-1338C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544248 | |||||||
| chr3:134544309 | T | C | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.556-1277T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544309 | |||||||
| chr3:134544333 | T | C | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.556-1253T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544333 | |||||||
| chr3:134544414 | T | A | 1 | a0001c0003t0003g0179 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.556-1172T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544414 | |||||||
| chr3:134544511 | C | T | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.556-1075C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544511 | |||||||
| chr3:134544631 | C | G | 1 | a0002c0002t0001g0253 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.556-955C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544631 | |||||||
| chr3:134544636 | T | G | 2 | a0001c0001t0011g0109 a0001c0001t0011g0111 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.556-950T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544636 | |||||||
| chr3:134544636 | T | TGG | 177 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(174): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.556-942_556-941dup others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134544636 | ||||||
| chr3:134544696 | A | G | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.556-890A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544696 | |||||||
| chr3:134544770 | G | A | 1 | a0002c0002t0001g0228 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.556-816G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544770 | |||||||
| chr3:134544895 | C | T | 1 | a0001c0001t0024g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.556-691C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544895 | |||||||
| chr3:134544957 | C | T | 1 | a0001c0001t0006g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.556-629C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134544957 | |||||||
| chr3:134545079 | C | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-507C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545079 | |||||||
| chr3:134545080 | A | G | 308 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.556-506A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545080 | |||||||
| chr3:134545148 | C | T | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.556-438C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545148 | |||||||
| chr3:134545149 | G | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.556-437G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545149 | |||||||
| chr3:134545200 | T | C | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.556-386T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545200 | |||||||
| chr3:134545218 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0018g0030 |
2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.556-368C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545218 | |||||||
| chr3:134545350 | G | A | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.556-236G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545350 | |||||||
| chr3:134545376 | T | C | 308 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.556-210T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545376 | |||||||
| chr3:134545450 | T | C | 1 | a0001c0003t0027g0163 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.556-136T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | chr3 | 134545450 | |||||||
| chr3:134545455 | AAT | A | 294 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(291): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.556-116_556-115del others(2): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 134545455 | ||||||
| chr3:134545886 | G | A | 1 | a0001c0003t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.789+67G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134545886 | |||||||
| chr3:134545924 | C | G | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.789+105C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134545924 | |||||||
| chr3:134545966 | T | C | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.789+147T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134545966 | |||||||
| chr3:134546008 | G | A | 1 | a0002c0002t0001g0283 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.790-141G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546008 | |||||||
| chr3:134546017 | A | C | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.790-132A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546017 | |||||||
| chr3:134546038 | G | C | 1 | a0008c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.790-111G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546038 | |||||||
| chr3:134546079 | C | A | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.790-70C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546079 | |||||||
| chr3:134546081 | G | A | 8 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(5): Show |
8 | HG00738.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.790-68G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546081 | |||||||
| chr3:134546113 | G | C | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.790-36G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 7/14 | chr3 | 134546113 | |||||||
| chr3:134546365 | T | A | 4 | a0002c0002t0001g0226 a0002c0002t0001g0237 a0002c0002t0001g0240 others(1): Show |
4 | HG01346.hp2 HG01993.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.929+77T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546365 | |||||||
| chr3:134546450 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.929+162C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546450 | |||||||
| chr3:134546451 | G | C | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.929+163G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546451 | |||||||
| chr3:134546678 | A | G | 1 | a0001c0003t0003g0156 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.929+390A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546678 | |||||||
| chr3:134546846 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.930-489G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546846 | |||||||
| chr3:134546907 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.930-428C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134546907 | |||||||
| chr3:134547001 | A | G | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.930-334A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134547001 | |||||||
| chr3:134547109 | A | G | 8 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.930-226A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134547109 | |||||||
| chr3:134547282 | A | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.930-53A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134547282 | |||||||
| chr3:134547306 | G | C | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.930-29G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 8/14 | chr3 | 134547306 | |||||||
| chr3:134547479 | A | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
splice_region_variant&intron_variant | LOW | c.1067+7A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547479 | |||||||
| chr3:134547485 | A | G | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1067+13A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547485 | |||||||
| chr3:134547605 | T | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1067+133T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547605 | |||||||
| chr3:134547614 | C | CTTTTTTT others(3): Show |
1 | a0002c0002t0001g0280 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1067+148_1067+157d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(6): Show |
5 | a0001c0001t0007g0114 a0001c0001t0007g0116 a0001c0001t0007g0117 others(2): Show |
5 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067+145_1067+157d others(15): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1067+144_1067+157d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(8): Show |
3 | a0001c0003t0003g0170 a0001c0003t0003g0171 a0008c0009t0001g0135 |
3 | HG03491.hp2 HG03492.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1067+143_1067+157d others(17): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(9): Show |
53 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(50): Show |
54 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(18): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(10): Show |
26 | a0001c0001t0001g0138 a0001c0001t0001g0149 a0001c0001t0001g0207 others(23): Show |
27 | HG01496.hp2 HG01891.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(19): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(11): Show |
11 | a0001c0001t0001g0148 a0001c0001t0001g0302 a0001c0001t0029g0136 others(8): Show |
11 | HG00741.hp1 HG02145.hp2 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(20): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(12): Show |
9 | a0001c0001t0001g0287 a0001c0001t0001g0305 a0001c0001t0001g0306 others(6): Show |
9 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(21): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(13): Show |
25 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0003t0003g0203 others(22): Show |
27 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(22): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(14): Show |
32 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0286 others(29): Show |
33 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(23): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(15): Show |
22 | a0002c0002t0001g0212 a0002c0002t0001g0213 a0002c0002t0001g0231 others(19): Show |
22 | HG00323.hp1 HG00738.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(24): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(16): Show |
5 | a0001c0001t0001g0300 a0002c0002t0001g0223 a0002c0002t0001g0238 others(2): Show |
5 | HG01168.hp1 HG01884.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1067+157_1067+158i others(25): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(17): Show |
1 | a0002c0002t0001g0292 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1067+157_1067+158i others(26): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | C | CTTTTTTT others(18): Show |
1 | a0002c0002t0001g0103 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1067+157_1067+158i others(27): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | CTT | C | 8 | a0001c0001t0005g0121 a0001c0001t0005g0122 a0001c0001t0005g0123 others(5): Show |
8 | HG03704.hp1 NA18940.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067+156_1067+157d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547614 | CTTT | C | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(91): Show |
99 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1067+155_1067+157d others(5): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134547614 | ||||||
| chr3:134547634 | C | T | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1067+162C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547634 | |||||||
| chr3:134547636 | G | C | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1067+164G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547636 | |||||||
| chr3:134547691 | A | G | 1 | a0001c0001t0024g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1067+219A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547691 | |||||||
| chr3:134547916 | C | G | 1 | a0001c0001t0004g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1067+444C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134547916 | |||||||
| chr3:134548144 | G | A | 1 | a0002c0002t0022g0246 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1067+672G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548144 | |||||||
| chr3:134548259 | T | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1067+787T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548259 | |||||||
| chr3:134548523 | T | A | 1 | a0002c0002t0001g0256 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1068-539T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548523 | |||||||
| chr3:134548650 | AGTAATAC others(7): Show |
A | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1068-409_1068-396d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 134548650 | ||||||
| chr3:134548677 | A | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1068-385A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548677 | |||||||
| chr3:134548810 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1068-252A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548810 | |||||||
| chr3:134548836 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1068-226C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 9/14 | chr3 | 134548836 | |||||||
| chr3:134549207 | T | C | 1 | a0008c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1182+31T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549207 | |||||||
| chr3:134549211 | A | G | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182+35A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549211 | |||||||
| chr3:134549329 | T | A | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1182+153T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549329 | |||||||
| chr3:134549357 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1182+181C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549357 | |||||||
| chr3:134549429 | A | T | 1 | a0002c0002t0001g0256 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1182+253A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549429 | |||||||
| chr3:134549777 | A | G | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1183-286A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549777 | |||||||
| chr3:134549782 | T | C | 2 | a0002c0002t0001g0224 a0002c0002t0001g0225 |
2 | HG00544.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1183-281T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549782 | |||||||
| chr3:134549857 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1183-206G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549857 | |||||||
| chr3:134549895 | A | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1183-168A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549895 | |||||||
| chr3:134549905 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1183-158T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134549905 | |||||||
| chr3:134550059 | A | G | 2 | a0002c0002t0001g0260 a0002c0002t0001g0262 |
2 | NA19006.hp2 NA19066.hp1 |
splice_region_variant&intron_variant | LOW | c.1183-4A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 10/14 | chr3 | 134550059 | |||||||
| chr3:134550318 | T | C | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1380+58T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550318 | |||||||
| chr3:134550396 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1380+136A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550396 | |||||||
| chr3:134550543 | G | T | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1380+283G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550543 | |||||||
| chr3:134550545 | T | A | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1380+285T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550545 | |||||||
| chr3:134550547 | G | A | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1380+287G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550547 | |||||||
| chr3:134550548 | C | A | 1 | a0001c0001t0004g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1380+288C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550548 | |||||||
| chr3:134550665 | CAAGTGGG others(8): Show |
C | 2 | a0001c0003t0001g0151 a0002c0002t0001g0270 |
2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1380+409_1380+423d others(17): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134550665 | ||||||
| chr3:134550699 | G | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1380+439G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550699 | |||||||
| chr3:134550800 | G | C | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1380+540G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550800 | |||||||
| chr3:134550958 | A | T | 1 | a0008c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1380+698A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134550958 | |||||||
| chr3:134551181 | AAT | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-743_1381-742d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551181 | ||||||
| chr3:134551231 | G | A | 8 | a0001c0001t0005g0120 a0001c0001t0005g0122 a0001c0001t0005g0123 others(5): Show |
8 | NA18940.hp2 NA18951.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1381-695G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551231 | |||||||
| chr3:134551286 | A | G | 2 | a0002c0002t0001g0241 a0002c0002t0001g0293 |
2 | NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1381-640A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551286 | |||||||
| chr3:134551314 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1381-612C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551314 | |||||||
| chr3:134551505 | A | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1381-421A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551505 | |||||||
| chr3:134551519 | T | C | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-407T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551519 | |||||||
| chr3:134551626 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1381-300T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551626 | |||||||
| chr3:134551724 | CAT | C | 4 | a0001c0001t0004g0102 a0001c0001t0004g0295 a0001c0001t0013g0088 others(1): Show |
4 | HG03017.hp1 HG03453.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-172_1381-171d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | ||||||
| chr3:134551724 | CATAT | C | 22 | a0001c0001t0002g0053 a0001c0001t0002g0071 a0001c0001t0002g0101 others(19): Show |
24 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1381-174_1381-171d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | ||||||
| chr3:134551724 | CATATAT | C | 65 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(62): Show |
68 | HG00140.hp2 HG00738.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.1381-176_1381-171d others(8): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | ||||||
| chr3:134551724 | CATATATA others(3): Show |
C | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1381-180_1381-171d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | ||||||
| chr3:134551724 | CATATATA others(7): Show |
C | 1 | a0002c0002t0001g0284 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1381-184_1381-171d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551724 | ||||||
| chr3:134551738 | TATATATA others(11): Show |
T | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-186_1381-169d others(20): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551738 | ||||||
| chr3:134551740 | TATATATA others(9): Show |
T | 83 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(80): Show |
85 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.1381-184_1381-169d others(18): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551740 | ||||||
| chr3:134551742 | TATATATA others(7): Show |
T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0211 a0001c0001t0001g0221 others(97): Show |
103 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1381-182_1381-169d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551742 | ||||||
| chr3:134551744 | TATATATA others(5): Show |
T | 13 | a0001c0001t0001g0216 a0001c0001t0001g0286 a0001c0001t0001g0287 others(10): Show |
13 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381-180_1381-169d others(14): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551744 | ||||||
| chr3:134551752 | T | C | 1 | a0001c0001t0005g0126 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1381-174T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551752 | |||||||
| chr3:134551754 | T | C | 16 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0036 others(13): Show |
16 | HG01106.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1381-172T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | chr3 | 134551754 | |||||||
| chr3:134551807 | G | GTA | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-108_1381-107d others(4): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 134551807 | ||||||
| chr3:134552044 | A | C | 46 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 others(43): Show |
46 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1467+32A>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552044 | |||||||
| chr3:134552092 | G | A | 1 | a0002c0002t0001g0242 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1467+80G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552092 | |||||||
| chr3:134552226 | G | A | 2 | a0001c0003t0003g0160 a0001c0003t0003g0176 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1467+214G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552226 | |||||||
| chr3:134552295 | C | G | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(87): Show |
95 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1467+283C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552295 | |||||||
| chr3:134552354 | C | G | 4 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+342C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552354 | |||||||
| chr3:134552384 | G | C | 1 | a0001c0001t0004g0019 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1467+372G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552384 | |||||||
| chr3:134552388 | A | G | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1467+376A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552388 | |||||||
| chr3:134552390 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1467+378G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552390 | |||||||
| chr3:134552432 | A | G | 1 | a0001c0001t0009g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1467+420A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552432 | |||||||
| chr3:134552750 | T | C | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1467+738T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552750 | |||||||
| chr3:134552907 | G | A | 19 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(16): Show |
19 | HG01169.hp1 HG01891.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.1467+895G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552907 | |||||||
| chr3:134552938 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1467+926C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134552938 | |||||||
| chr3:134553167 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(3): Show |
6 | NA18941.hp2 NA18955.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1467+1155G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553167 | |||||||
| chr3:134553214 | G | A | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1467+1202G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553214 | |||||||
| chr3:134553447 | A | T | 1 | a0002c0002t0001g0248 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1467+1435A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553447 | |||||||
| chr3:134553518 | G | A | 3 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0054 |
4 | NA18949.hp1 NA18960.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+1506G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553518 | |||||||
| chr3:134553566 | T | C | 1 | a0001c0003t0003g0179 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1467+1554T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553566 | |||||||
| chr3:134553660 | T | A | 16 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0021 others(13): Show |
16 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1467+1648T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553660 | |||||||
| chr3:134553716 | A | G | 1 | a0005c0013t0007g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1467+1704A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553716 | |||||||
| chr3:134553779 | A | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1467+1767A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553779 | |||||||
| chr3:134553874 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1467+1862G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553874 | |||||||
| chr3:134553930 | T | TAA | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1467+1919_1467+192 others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134553930 | ||||||
| chr3:134553941 | C | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1467+1929C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553941 | |||||||
| chr3:134553943 | A | G | 9 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG03704.hp1 NA18940.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.1467+1931A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134553943 | |||||||
| chr3:134554018 | C | G | 1 | a0002c0002t0001g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1467+2006C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554018 | |||||||
| chr3:134554023 | C | T | 1 | a0008c0009t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1467+2011C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554023 | |||||||
| chr3:134554042 | G | A | 309 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(306): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1467+2030G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554042 | |||||||
| chr3:134554066 | C | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+2054C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554066 | |||||||
| chr3:134554173 | A | G | 303 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1467+2161A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554173 | |||||||
| chr3:134554185 | A | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1467+2173A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554185 | |||||||
| chr3:134554232 | C | G | 1 | a0004c0007t0003g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1467+2220C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554232 | |||||||
| chr3:134554238 | C | A | 1 | a0002c0002t0001g0244 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1467+2226C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554238 | |||||||
| chr3:134554268 | G | A | 2 | a0001c0001t0019g0061 a0001c0001t0020g0092 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1467+2256G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554268 | |||||||
| chr3:134554304 | A | G | 191 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(188): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1467+2292A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554304 | |||||||
| chr3:134554471 | C | T | 307 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(304): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1467+2459C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554471 | |||||||
| chr3:134554485 | G | C | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+2473G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554485 | |||||||
| chr3:134554502 | C | G | 1 | a0001c0003t0001g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1467+2490C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554502 | |||||||
| chr3:134554655 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1467+2643C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554655 | |||||||
| chr3:134554684 | C | G | 1 | a0001c0003t0003g0200 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1467+2672C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554684 | |||||||
| chr3:134554904 | G | A | 1 | a0001c0001t0006g0081 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1467+2892G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134554904 | |||||||
| chr3:134555116 | C | T | 51 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 others(48): Show |
52 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1468-3026C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555116 | |||||||
| chr3:134555117 | G | A | 15 | a0001c0001t0001g0211 a0001c0001t0001g0221 a0001c0001t0001g0264 others(12): Show |
15 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1468-3025G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555117 | |||||||
| chr3:134555349 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1468-2793G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555349 | |||||||
| chr3:134555360 | A | G | 3 | a0001c0001t0011g0109 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG02559.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1468-2782A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555360 | |||||||
| chr3:134555496 | C | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1468-2646C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555496 | |||||||
| chr3:134555517 | T | C | 1 | a0001c0003t0003g0179 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1468-2625T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555517 | |||||||
| chr3:134555563 | C | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1468-2579C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555563 | |||||||
| chr3:134555646 | A | G | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG01496.hp2 HG02280.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-2496A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555646 | |||||||
| chr3:134555811 | G | A | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-2331G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555811 | |||||||
| chr3:134555855 | C | T | 303 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(300): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1468-2287C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555855 | |||||||
| chr3:134555878 | A | G | 202 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(199): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1468-2264A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555878 | |||||||
| chr3:134555969 | G | A | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1468-2173G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134555969 | |||||||
| chr3:134556068 | C | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1468-2074C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556068 | |||||||
| chr3:134556110 | T | G | 12 | a0001c0001t0001g0211 a0001c0001t0001g0221 a0001c0001t0001g0263 others(9): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468-2032T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556110 | |||||||
| chr3:134556276 | G | T | 1 | a0002c0002t0001g0228 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1468-1866G>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556276 | |||||||
| chr3:134556302 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1468-1840T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556302 | |||||||
| chr3:134556303 | A | G | 1 | a0002c0002t0001g0209 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1468-1839A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556303 | |||||||
| chr3:134556304 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1468-1838C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556304 | |||||||
| chr3:134556384 | G | A | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1468-1758G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556384 | |||||||
| chr3:134556453 | G | C | 1 | a0003c0006t0001g0222 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1468-1689G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556453 | |||||||
| chr3:134556479 | A | G | 1 | a0002c0002t0001g0103 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1468-1663A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556479 | |||||||
| chr3:134556502 | A | G | 1 | a0001c0001t0025g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1468-1640A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556502 | |||||||
| chr3:134556518 | A | T | 1 | a0001c0003t0001g0134 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1468-1624A>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556518 | |||||||
| chr3:134556605 | G | C | 9 | a0002c0002t0001g0214 a0002c0002t0001g0223 a0002c0002t0001g0238 others(6): Show |
9 | HG00735.hp1 HG01099.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1468-1537G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556605 | |||||||
| chr3:134556759 | G | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1468-1383G>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556759 | |||||||
| chr3:134556778 | G | A | 1 | a0001c0003t0003g0169 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1468-1364G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134556778 | |||||||
| chr3:134557252 | A | G | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1468-890A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557252 | |||||||
| chr3:134557376 | G | GT | 30 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0022 others(27): Show |
31 | HG00544.hp2 HG01106.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1468-738dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | G | GTTTTTTT others(2): Show |
11 | a0001c0003t0003g0155 a0001c0003t0003g0170 a0001c0003t0003g0184 others(8): Show |
12 | HG00280.hp1 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1468-746_1468-738d others(11): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | G | GTTTTTTT others(3): Show |
34 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0003t0001g0141 others(31): Show |
34 | HG00735.hp2 HG01106.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1468-747_1468-738d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | G | GTTTTTTT others(4): Show |
23 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0133 others(20): Show |
23 | HG00423.hp1 HG00741.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1468-748_1468-738d others(13): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | G | GTTTTTTT others(5): Show |
10 | a0001c0001t0001g0137 a0001c0001t0001g0148 a0001c0001t0001g0149 others(7): Show |
11 | HG02622.hp2 HG02809.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1468-749_1468-738d others(14): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | G | GTTTTTTT others(6): Show |
2 | a0001c0001t0001g0207 a0001c0003t0001g0152 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1468-750_1468-738d others(15): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | G | GTTTTTTT others(7): Show |
3 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0099 |
3 | HG01891.hp1 HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1468-751_1468-738d others(16): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1468-755_1468-738d others(20): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | GT | G | 10 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(7): Show |
12 | NA18955.hp2 NA18960.hp2 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468-738delT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | GTTTT | G | 80 | a0002c0002t0001g0002 a0002c0002t0001g0103 a0002c0002t0001g0209 others(77): Show |
82 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1468-741_1468-738d others(6): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | GTTTTTTT others(3): Show |
G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0286 others(13): Show |
17 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.1468-747_1468-738d others(12): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557376 | GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1468-748_1468-738d others(13): Show |
CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 134557376 | ||||||
| chr3:134557382 | T | G | 1 | a0001c0001t0021g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1468-760T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557382 | |||||||
| chr3:134557387 | T | G | 2 | a0002c0002t0001g0234 a0002c0002t0001g0262 |
2 | NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1468-755T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557387 | |||||||
| chr3:134557388 | T | G | 78 | a0002c0002t0001g0002 a0002c0002t0001g0103 a0002c0002t0001g0209 others(75): Show |
80 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1468-754T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557388 | |||||||
| chr3:134557404 | T | A | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1468-738T>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557404 | |||||||
| chr3:134557500 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1468-642C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557500 | |||||||
| chr3:134557623 | C | G | 1 | a0001c0001t0020g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1468-519C>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557623 | |||||||
| chr3:134557638 | A | G | 7 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468-504A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557638 | |||||||
| chr3:134557791 | G | A | 6 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(3): Show |
6 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468-351G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557791 | |||||||
| chr3:134557865 | C | A | 1 | a0001c0001t0002g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1468-277C>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557865 | |||||||
| chr3:134557963 | A | G | 1 | a0002c0002t0001g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1468-179A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 12/14 | chr3 | 134557963 | |||||||
| chr3:134558353 | A | AT | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1673+12dupT | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 134558353 | ||||||
| chr3:134558457 | A | G | 1 | a0001c0001t0007g0114 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1673+110A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558457 | |||||||
| chr3:134558459 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1673+112G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558459 | |||||||
| chr3:134558485 | A | G | 1 | a0001c0001t0024g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1673+138A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558485 | |||||||
| chr3:134558558 | A | G | 4 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1673+211A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558558 | |||||||
| chr3:134558898 | T | C | 82 | a0002c0002t0001g0002 a0002c0002t0001g0103 a0002c0002t0001g0209 others(79): Show |
84 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1674-252T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558898 | |||||||
| chr3:134558960 | T | G | 8 | a0001c0001t0005g0120 a0001c0001t0005g0122 a0001c0001t0005g0123 others(5): Show |
8 | NA18940.hp2 NA18951.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1674-190T>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 13/14 | chr3 | 134558960 | |||||||
| chr3:134559461 | T | C | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG02572.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1953+32T>C | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134559461 | |||||||
| chr3:134559761 | A | G | 1 | a0001c0001t0005g0121 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1953+332A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134559761 | |||||||
| chr3:134559803 | G | A | 1 | a0002c0002t0001g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1953+374G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134559803 | |||||||
| chr3:134559863 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1953+434G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134559863 | |||||||
| chr3:134560225 | A | G | 3 | a0001c0001t0012g0105 a0001c0001t0012g0106 a0001c0001t0012g0107 |
3 | HG01123.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1953+796A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560225 | |||||||
| chr3:134560275 | C | T | 3 | a0001c0001t0010g0086 a0001c0001t0010g0090 a0001c0001t0010g0091 |
3 | HG01891.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1953+846C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560275 | |||||||
| chr3:134560355 | A | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0009 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1953+926A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560355 | |||||||
| chr3:134560437 | C | T | 3 | a0001c0003t0008g0007 a0001c0003t0008g0180 a0001c0003t0008g0199 |
4 | HG01256.hp2 HG01258.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954-940C>T | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560437 | |||||||
| chr3:134560529 | G | A | 83 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(80): Show |
85 | HG00280.hp1 HG00423.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.1954-848G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560529 | |||||||
| chr3:134560729 | A | G | 1 | a0001c0001t0019g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1954-648A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560729 | |||||||
| chr3:134560835 | A | G | 82 | a0002c0002t0001g0002 a0002c0002t0001g0103 a0002c0002t0001g0209 others(79): Show |
84 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1954-542A>G | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134560835 | |||||||
| chr3:134561315 | G | A | 2 | a0001c0003t0003g0165 a0007c0008t0003g0182 |
2 | HG02015.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1954-62G>A | CEP63 | ENSG00000182923.20 | transcript | ENST00000675561.1 | protein_coding | 14/14 | chr3 | 134561315 |