Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26259 |
| ensemblid | ENSG00000174989.13 |
| hgncid | 13597 |
| symbol | FBXW8 |
| name | F-box and WD repeat domain containing 8 |
| refseq_nuc | NM_153348.3 |
| refseq_prot | NP_699179.2 |
| ensembl_nuc | ENST00000652555.1 |
| ensembl_prot | ENSP00000498999.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 116910950 |
| end | 117031148 |
| strand | + |
| ver | v1.2 |
| region | chr12:116910950-117031148 |
| region5000 | chr12:116905950-117036148 |
| regionname0 | FBXW8_chr12_116910950_117031148 |
| regionname5000 | FBXW8_chr12_116905950_117036148 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 598 | 138 | 20 | 23 | 62 | 4 | 28 | 39 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0002 | 1/0 | 598 | 93 | 35 | 9 | 39 | 2 | 7 | 32 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0003 | 0/0 | 598 | 32 | 29 | 1 | 0 | 0 | 2 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0004 | 0/0 | 598 | 12 | 0 | 0 | 12 | 0 | 0 | 8 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0005 | 0/0 | 598 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0006 | 0/0 | 598 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0007 | 0/0 | 72 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(67): Show |
chr12 | 116905950 | 117036148 |
| a0008 | 0/0 | 598 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0009 | 0/0 | 598 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0010 | 0/0 | 598 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0011 | 0/0 | 598 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| a0012 | 0/0 | 598 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | MDDYS others(593): Show |
chr12 | 116905950 | 117036148 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1794 | 129 | 20 | 18 | 62 | 4 | 24 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0001c0006 | 0/0 | 1794 | 6 | 0 | 5 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0001c0009 | 0/0 | 1794 | 3 | 0 | 0 | 0 | 0 | 3 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0002c0002 | 0/0 | 1794 | 86 | 34 | 7 | 37 | 1 | 7 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0002c0008 | 0/0 | 1794 | 4 | 1 | 2 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0002c0011 | 0/0 | 1794 | 2 | 0 | 0 | 2 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0002c0013 | 1/0 | 1794 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0003c0003 | 0/0 | 1794 | 24 | 21 | 1 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0003c0005 | 0/0 | 1794 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0003c0020 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0003c0021 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0004c0004 | 0/0 | 1794 | 12 | 0 | 0 | 12 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0005c0007 | 0/0 | 1794 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0005c0017 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0006c0010 | 0/0 | 1794 | 2 | 1 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0007c0012 | 0/0 | 1775 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1770): Show |
chr12 | 116905950 | 117036148 | ||
| a0008c0018 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0009c0016 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0010c0019 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0011c0015 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 | ||
| a0012c0014 | 0/0 | 1794 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | ATGGA others(1789): Show |
chr12 | 116905950 | 117036148 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4861 | 69 | 9 | 10 | 37 | 3 | 9 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0003 | 0/0 | 4861 | 34 | 8 | 6 | 15 | 1 | 4 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0004 | 0/0 | 4859 | 16 | 0 | 0 | 8 | 0 | 8 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4854): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0014 | 0/0 | 4861 | 2 | 0 | 0 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0015 | 0/0 | 4861 | 2 | 0 | 1 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0025 | 0/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0031 | 0/0 | 4861 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0032 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0033 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4853): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0034 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0001t0035 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0006t0001 | 0/0 | 4861 | 6 | 0 | 5 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0001c0009t0001 | 0/0 | 4861 | 3 | 0 | 0 | 0 | 0 | 3 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0001 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0002 | 0/0 | 4861 | 54 | 19 | 3 | 30 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0005 | 0/0 | 4859 | 10 | 0 | 2 | 3 | 1 | 4 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4854): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0008 | 0/0 | 4861 | 6 | 5 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0009 | 0/0 | 4871 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4866): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0011 | 0/0 | 4858 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4853): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0016 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0022 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0024 | 0/0 | 4861 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0026 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0027 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0028 | 0/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0002t0030 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0008t0002 | 0/0 | 4861 | 4 | 1 | 2 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0011t0002 | 0/0 | 4861 | 2 | 0 | 0 | 2 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0002c0013t0001 | 1/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0001 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0003 | 0/0 | 4861 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0006 | 0/0 | 4861 | 8 | 8 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0010 | 0/0 | 4861 | 5 | 3 | 0 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0011 | 0/0 | 4858 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4853): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0012 | 0/0 | 4861 | 3 | 3 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0019 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0021 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0003t0029 | 0/0 | 4861 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0005t0002 | 0/0 | 4861 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0020t0020 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0003c0021t0017 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0004c0004t0001 | 0/0 | 4861 | 12 | 0 | 0 | 12 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0005c0007t0002 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0005c0007t0007 | 0/0 | 4861 | 5 | 5 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0005c0017t0007 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0006c0010t0013 | 0/0 | 4861 | 2 | 1 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0007c0012t0018 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4834): Show |
chr12 | 116905950 | 117036148 |
| a0008c0018t0002 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0009c0016t0003 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0010c0019t0003 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0011c0015t0003 | 0/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| a0012c0014t0023 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | CCGGC others(4856): Show |
chr12 | 116905950 | 117036148 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0014g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0014g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0015g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0025g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0031g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0032g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0033g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0034g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0035g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0009t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0009t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0009t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0009g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0011g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0016g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0022g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0024g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0026g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0027g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0028g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0030g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0008t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0008t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0008t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0008t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0011t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0011t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0013t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0019g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0021g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0029g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0020t0020g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0021t0017g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0017t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0006c0010t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0006c0010t0013g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0007c0012t0018g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0008c0018t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0009c0016t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0010c0019t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0011c0015t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0012c0014t0023g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0201 | EUR | GBR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00323 | hp1 | a0002 | c0002 | t0005 | g0094 | EUR | FIN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00423 | hp2 | a0004 | c0004 | t0001 | g0255 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00438 | hp1 | a0004 | c0004 | t0001 | g0256 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00642 | hp1 | a0001 | c0006 | t0001 | g0183 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00642 | hp2 | a0002 | c0002 | t0005 | g0101 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00741 | hp1 | a0003 | c0003 | t0029 | g0018 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00741 | hp2 | a0001 | c0006 | t0001 | g0245 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01074 | hp1 | a0006 | c0010 | t0013 | g0109 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01106 | hp1 | a0002 | c0002 | t0008 | g0137 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01106 | hp2 | a0001 | c0006 | t0001 | g0270 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01168 | hp1 | a0001 | c0006 | t0001 | g0224 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01175 | hp1 | a0002 | c0002 | t0024 | g0065 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01256 | hp2 | a0002 | c0002 | t0005 | g0100 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01258 | hp2 | a0001 | c0001 | t0015 | g0220 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01261 | hp1 | a0002 | c0008 | t0002 | g0070 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01261 | hp2 | a0001 | c0001 | t0031 | g0049 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0133 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01358 | hp2 | a0001 | c0006 | t0001 | g0284 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01884 | hp1 | a0003 | c0003 | t0012 | g0020 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01884 | hp2 | a0005 | c0017 | t0007 | g0027 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0135 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01891 | hp2 | a0003 | c0003 | t0011 | g0011 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02027 | hp1 | a0004 | c0004 | t0001 | g0267 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02055 | hp1 | a0001 | c0001 | t0032 | g0046 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02055 | hp2 | a0007 | c0012 | t0018 | g0012 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02135 | hp2 | a0004 | c0004 | t0001 | g0280 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02145 | hp1 | a0003 | c0003 | t0019 | g0024 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02145 | hp2 | a0005 | c0007 | t0007 | g0023 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02148 | hp1 | a0002 | c0008 | t0002 | g0067 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | CDX | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | CDX | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02257 | hp1 | a0002 | c0002 | t0008 | g0069 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02257 | hp2 | a0003 | c0005 | t0002 | g0059 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02258 | hp1 | a0001 | c0001 | t0033 | g0248 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02258 | hp2 | a0002 | c0002 | t0011 | g0082 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02280 | hp1 | a0002 | c0002 | t0009 | g0062 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02280 | hp2 | a0005 | c0007 | t0007 | g0002 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02572 | hp1 | a0003 | c0003 | t0010 | g0016 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02572 | hp2 | a0003 | c0003 | t0010 | g0013 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0093 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02602 | hp2 | a0001 | c0006 | t0001 | g0271 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02615 | hp1 | a0003 | c0003 | t0006 | g0008 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02615 | hp2 | a0003 | c0021 | t0017 | g0005 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02622 | hp2 | a0002 | c0002 | t0008 | g0136 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0098 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02647 | hp1 | a0005 | c0007 | t0007 | g0025 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0145 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02698 | hp1 | a0001 | c0009 | t0001 | g0246 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02698 | hp2 | a0001 | c0001 | t0014 | g0162 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0089 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0087 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02723 | hp2 | a0003 | c0003 | t0006 | g0004 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02738 | hp1 | a0002 | c0002 | t0005 | g0064 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02738 | hp2 | a0002 | c0002 | t0028 | g0063 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02886 | hp1 | a0003 | c0003 | t0006 | g0006 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02886 | hp2 | a0002 | c0002 | t0009 | g0001 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02897 | hp2 | a0003 | c0003 | t0010 | g0014 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02922 | hp1 | a0003 | c0005 | t0002 | g0058 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02965 | hp2 | a0002 | c0002 | t0009 | g0060 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02970 | hp1 | a0002 | c0002 | t0027 | g0140 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02970 | hp2 | a0003 | c0003 | t0012 | g0021 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0132 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0161 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03017 | hp2 | a0001 | c0001 | t0025 | g0273 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03041 | hp2 | a0005 | c0007 | t0007 | g0002 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0106 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03130 | hp2 | a0002 | c0002 | t0009 | g0001 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0150 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03195 | hp1 | a0003 | c0005 | t0002 | g0055 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03195 | hp2 | a0002 | c0002 | t0009 | g0061 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03209 | hp1 | a0003 | c0003 | t0006 | g0004 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03209 | hp2 | a0003 | c0020 | t0020 | g0081 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0283 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03225 | hp2 | a0003 | c0003 | t0012 | g0022 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03239 | hp2 | a0003 | c0003 | t0010 | g0017 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03453 | hp1 | a0003 | c0003 | t0003 | g0192 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0099 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03486 | hp1 | a0001 | c0001 | t0035 | g0175 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03486 | hp2 | a0003 | c0003 | t0021 | g0007 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03490 | hp1 | a0002 | c0002 | t0005 | g0134 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03516 | hp1 | a0009 | c0016 | t0003 | g0029 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03516 | hp2 | a0002 | c0002 | t0011 | g0147 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03540 | hp1 | a0002 | c0002 | t0008 | g0110 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03540 | hp2 | a0003 | c0003 | t0006 | g0152 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03579 | hp1 | a0010 | c0019 | t0003 | g0193 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0040 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0122 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0042 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03710 | hp2 | a0003 | c0003 | t0010 | g0019 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03942 | hp1 | a0002 | c0002 | t0005 | g0103 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03942 | hp2 | a0001 | c0009 | t0001 | g0187 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04228 | hp1 | a0011 | c0015 | t0003 | g0196 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18522 | hp1 | a0005 | c0007 | t0002 | g0026 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18522 | hp2 | a0002 | c0002 | t0009 | g0001 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | CHB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0166 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18906 | hp2 | a0006 | c0010 | t0013 | g0108 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18949 | hp2 | a0012 | c0014 | t0023 | g0078 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18956 | hp2 | a0004 | c0004 | t0001 | g0178 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18965 | hp2 | a0004 | c0004 | t0001 | g0260 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18967 | hp1 | a0002 | c0011 | t0002 | g0130 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18967 | hp2 | a0004 | c0004 | t0001 | g0160 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18975 | hp1 | a0002 | c0002 | t0005 | g0092 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18980 | hp1 | a0002 | c0002 | t0005 | g0107 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18993 | hp1 | a0001 | c0001 | t0034 | g0172 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18994 | hp1 | a0002 | c0002 | t0030 | g0128 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18994 | hp2 | a0004 | c0004 | t0001 | g0254 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18997 | hp2 | a0004 | c0004 | t0001 | g0281 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19005 | hp1 | a0004 | c0004 | t0001 | g0249 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19005 | hp2 | a0002 | c0011 | t0002 | g0142 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19030 | hp1 | a0005 | c0007 | t0007 | g0028 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19030 | hp2 | a0002 | c0002 | t0022 | g0097 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0104 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19058 | hp2 | a0002 | c0002 | t0026 | g0071 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19068 | hp2 | a0004 | c0004 | t0001 | g0258 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19080 | hp1 | a0002 | c0002 | t0016 | g0112 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19080 | hp2 | a0002 | c0002 | t0005 | g0124 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19090 | hp1 | a0004 | c0004 | t0001 | g0185 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19240 | hp1 | a0003 | c0003 | t0006 | g0153 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20129 | hp1 | a0003 | c0003 | t0011 | g0010 | AFR | ASW | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20129 | hp2 | a0003 | c0005 | t0002 | g0056 | AFR | ASW | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20805 | hp2 | a0002 | c0008 | t0002 | g0068 | EUR | TSI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20905 | hp1 | a0001 | c0009 | t0001 | g0250 | SAS | GIH | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20905 | hp2 | a0002 | c0002 | t0005 | g0149 | SAS | GIH | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02109 | hp1 | a0008 | c0018 | t0002 | g0015 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0091 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02486 | hp1 | a0003 | c0005 | t0002 | g0054 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02559 | hp2 | a0002 | c0002 | t0008 | g0083 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03471 | hp1 | a0003 | c0003 | t0006 | g0151 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03471 | hp2 | a0002 | c0002 | t0008 | g0111 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | USA | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0105 | AFR | USA | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18955 | hp2 | a0001 | c0001 | t0015 | g0261 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | USA | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20300 | hp2 | a0003 | c0003 | t0006 | g0009 | AFR | USA | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA21309 | hp1 | a0003 | c0005 | t0002 | g0057 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA21309 | hp2 | a0002 | c0008 | t0002 | g0066 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0158 | REF | REF | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| homoSapiens | grch38p0 | a0002 | c0013 | t0001 | g0102 | REF | REF | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116911140 | CGGGCTCG others(12): Show |
C | 1 | a0007 | 1 | HG02055.hp2 | frameshift_variant | HIGH | c.110_128delGGCGGCCG others(11): Show |
p.Arg37fs | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 198/4861 | 110/1797 | 37/598 | INFO_REALIGN_3_PRIME | chr12 | 116911140 | ||
| chr12:116911209 | C | G | 9 | a0001 a0003 a0004 others(6): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(190): Show |
missense_variant | MODERATE | c.172C>G | p.Arg58Gly | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 260/4861 | 172/1797 | 58/598 | chr12 | 116911209 | |||
| chr12:116945515 | G | A | 6 | a0001 a0004 a0005 others(3): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
missense_variant | MODERATE | c.575G>A | p.Arg192Gln | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/11 | 663/4861 | 575/1797 | 192/598 | chr12 | 116945515 | |||
| chr12:116949660 | A | G | 1 | a0005 | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
missense_variant | MODERATE | c.631A>G | p.Thr211Ala | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/11 | 719/4861 | 631/1797 | 211/598 | chr12 | 116949660 | |||
| chr12:116985235 | G | A | 1 | a0008 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.865G>A | p.Gly289Arg | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/11 | 953/4861 | 865/1797 | 289/598 | chr12 | 116985235 | |||
| chr12:117010353 | C | T | 1 | a0009 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1270C>T | p.Arg424Cys | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/11 | 1358/4861 | 1270/1797 | 424/598 | chr12 | 117010353 | |||
| chr12:117027419 | A | G | 2 | a0006 a0010 |
3 | HG01074.hp1 HG03579.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1567A>G | p.Ser523Gly | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/11 | 1655/4861 | 1567/1797 | 523/598 | chr12 | 117027419 | |||
| chr12:117027459 | C | T | 1 | a0004 | 12 | HG00423.hp2 HG00438.hp1 HG02027.hp1 others(9): Show |
missense_variant | MODERATE | c.1607C>T | p.Thr536Met | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/11 | 1695/4861 | 1607/1797 | 536/598 | chr12 | 117027459 | |||
| chr12:117027468 | G | A | 1 | a0011 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1616G>A | p.Arg539Gln | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/11 | 1704/4861 | 1616/1797 | 539/598 | chr12 | 117027468 | |||
| chr12:117028032 | C | T | 1 | a0012 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1657C>T | p.Arg553Trp | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1745/4861 | 1657/1797 | 553/598 | chr12 | 117028032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116911163 | C | A | 1 | a0002c0008 | 4 | HG01261.hp1 HG02148.hp1 NA20805.hp2 others(1): Show |
synonymous_variant | LOW | c.126C>A | p.Gly42Gly | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 214/4861 | 126/1797 | 42/598 | chr12 | 116911163 | |||
| chr12:116911271 | C | T | 1 | a0003c0021 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.234C>T | p.Asp78Asp | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 322/4861 | 234/1797 | 78/598 | chr12 | 116911271 | |||
| chr12:116911340 | G | A | 1 | a0003c0005 | 6 | HG02257.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
synonymous_variant | LOW | c.303G>A | p.Gln101Gln | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 391/4861 | 303/1797 | 101/598 | chr12 | 116911340 | |||
| chr12:116985264 | C | T | 1 | a0003c0020 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.894C>T | p.His298His | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/11 | 982/4861 | 894/1797 | 298/598 | chr12 | 116985264 | |||
| chr12:116985400 | C | T | 1 | a0005c0017 | 1 | HG01884.hp2 | splice_region_variant&synonymous_variant | LOW | c.1030C>T | p.Leu344Leu | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/11 | 1118/4861 | 1030/1797 | 344/598 | chr12 | 116985400 | |||
| chr12:117024273 | C | T | 1 | a0002c0011 | 2 | NA18967.hp1 NA19005.hp2 |
synonymous_variant | LOW | c.1494C>T | p.Ser498Ser | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/11 | 1582/4861 | 1494/1797 | 498/598 | chr12 | 117024273 | |||
| chr12:117028046 | C | T | 1 | a0001c0009 | 3 | HG02698.hp1 HG03942.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.1671C>T | p.Arg557Arg | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1759/4861 | 1671/1797 | 557/598 | chr12 | 117028046 | |||
| chr12:117028052 | T | C | 19 | a0001c0001 a0001c0009 a0002c0002 others(16): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
synonymous_variant | LOW | c.1677T>C | p.Tyr559Tyr | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1765/4861 | 1677/1797 | 559/598 | chr12 | 117028052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116910966 | C | T | 1 | a0002c0002t0009 | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-72C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 72 | chr12 | 116910966 | ||||||
| chr12:117028176 | T | C | 38 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0025 others(35): Show |
188 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*4T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 4 | chr12 | 117028176 | ||||||
| chr12:117028307 | C | T | 1 | a0002c0002t0030 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*135C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 135 | chr12 | 117028307 | ||||||
| chr12:117028462 | G | A | 1 | a0002c0002t0016 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 290 | chr12 | 117028462 | ||||||
| chr12:117028466 | C | T | 2 | a0003c0003t0010 a0003c0003t0029 |
6 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*294C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 294 | chr12 | 117028466 | ||||||
| chr12:117028468 | C | T | 1 | a0002c0002t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 296 | chr12 | 117028468 | ||||||
| chr12:117028695 | G | A | 2 | a0001c0001t0031 a0001c0001t0032 |
2 | HG01261.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*523G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 523 | chr12 | 117028695 | ||||||
| chr12:117028757 | T | C | 4 | a0002c0002t0011 a0003c0003t0011 a0003c0021t0017 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*585T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 585 | chr12 | 117028757 | ||||||
| chr12:117029004 | A | G | 1 | a0003c0003t0029 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 832 | chr12 | 117029004 | ||||||
| chr12:117029116 | A | G | 1 | a0002c0002t0027 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*944A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 944 | chr12 | 117029116 | ||||||
| chr12:117029162 | C | G | 1 | a0001c0001t0035 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*990C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 990 | chr12 | 117029162 | ||||||
| chr12:117029212 | C | G | 1 | a0001c0001t0032 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1040C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1040 | chr12 | 117029212 | ||||||
| chr12:117029255 | C | T | 1 | a0007c0012t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1083C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1083 | chr12 | 117029255 | ||||||
| chr12:117029311 | T | A | 2 | a0003c0003t0019 a0003c0020t0020 |
2 | HG02145.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1139 | chr12 | 117029311 | ||||||
| chr12:117029320 | G | A | 4 | a0003c0003t0006 a0003c0003t0010 a0003c0003t0021 others(1): Show |
15 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1148G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1148 | chr12 | 117029320 | ||||||
| chr12:117029394 | A | G | 5 | a0002c0002t0011 a0003c0003t0011 a0003c0003t0012 others(2): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1222A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1222 | chr12 | 117029394 | ||||||
| chr12:117029409 | ACT | A | 1 | a0002c0002t0005 | 10 | HG00323.hp1 HG00642.hp2 HG01256.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1242_*1243delCT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1242 | INFO_REALIGN_3_PRIME | chr12 | 117029409 | |||||
| chr12:117029460 | T | TGGGGCTG others(3): Show |
1 | a0002c0002t0009 | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1296_*1305dupGGAG others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1306 | INFO_REALIGN_3_PRIME | chr12 | 117029460 | |||||
| chr12:117029478 | T | G | 1 | a0001c0001t0014 | 2 | HG02698.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1306T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1306 | chr12 | 117029478 | ||||||
| chr12:117029567 | G | A | 29 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(26): Show |
129 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1395G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1395 | chr12 | 117029567 | ||||||
| chr12:117029635 | C | T | 1 | a0002c0002t0008 | 6 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1463C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1463 | chr12 | 117029635 | ||||||
| chr12:117029700 | C | T | 1 | a0002c0002t0024 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1528C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1528 | chr12 | 117029700 | ||||||
| chr12:117030136 | C | T | 1 | a0003c0020t0020 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1964 | chr12 | 117030136 | ||||||
| chr12:117030260 | C | T | 1 | a0012c0014t0023 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2088 | chr12 | 117030260 | ||||||
| chr12:117030306 | G | A | 1 | a0006c0010t0013 | 2 | HG01074.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2134G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2134 | chr12 | 117030306 | ||||||
| chr12:117030463 | TTC | T | 1 | a0001c0001t0004 | 16 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2298_*2299delTC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2298 | INFO_REALIGN_3_PRIME | chr12 | 117030463 | |||||
| chr12:117030534 | A | G | 1 | a0002c0002t0022 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2362A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2362 | chr12 | 117030534 | ||||||
| chr12:117030541 | G | A | 1 | a0002c0002t0030 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2369G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2369 | chr12 | 117030541 | ||||||
| chr12:117030547 | A | T | 1 | a0001c0001t0034 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2375 | chr12 | 117030547 | ||||||
| chr12:117030562 | C | G | 29 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(26): Show |
129 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2390C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2390 | chr12 | 117030562 | ||||||
| chr12:117030600 | C | T | 1 | a0001c0001t0015 | 2 | HG01258.hp2 NA18955.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2428C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2428 | chr12 | 117030600 | ||||||
| chr12:117030630 | G | C | 1 | a0003c0003t0021 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2458G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2458 | chr12 | 117030630 | ||||||
| chr12:117030668 | G | A | 1 | a0003c0020t0020 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2496G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2496 | chr12 | 117030668 | ||||||
| chr12:117030751 | T | G | 2 | a0003c0003t0010 a0003c0003t0029 |
6 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2579T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2579 | chr12 | 117030751 | ||||||
| chr12:117030958 | CCTT | C | 4 | a0001c0001t0033 a0002c0002t0011 a0003c0003t0011 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2790_*2792delCTT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2790 | INFO_REALIGN_3_PRIME | chr12 | 117030958 | |||||
| chr12:117030993 | C | T | 3 | a0002c0002t0008 a0005c0007t0007 a0005c0017t0007 |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2821C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2821 | chr12 | 117030993 | ||||||
| chr12:117031068 | A | G | 37 | a0001c0001t0003 a0001c0001t0004 a0002c0002t0002 others(34): Show |
187 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*2896A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2896 | chr12 | 117031068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116911670 | A | G | 131 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0001g0164 others(128): Show |
131 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.318+315A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116911670 | |||||||
| chr12:116912052 | A | G | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+697A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912052 | |||||||
| chr12:116912062 | G | C | 22 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+707G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912062 | |||||||
| chr12:116912171 | GT | G | 161 | a0001c0001t0001g0048 a0001c0001t0001g0159 a0001c0001t0001g0164 others(158): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.318+831delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912171 | ||||||
| chr12:116912171 | GTT | G | 11 | a0001c0001t0001g0157 a0001c0001t0003g0154 a0001c0001t0003g0155 others(8): Show |
12 | HG01884.hp2 HG02040.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.318+830_318+831del others(2): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912171 | ||||||
| chr12:116912183 | T | C | 22 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+828T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912183 | |||||||
| chr12:116912336 | C | G | 1 | a0003c0003t0001g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.318+981C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912336 | |||||||
| chr12:116912377 | A | G | 1 | a0002c0002t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.318+1022A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912377 | |||||||
| chr12:116912432 | C | T | 1 | a0002c0002t0005g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.318+1077C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912432 | |||||||
| chr12:116912450 | TC | T | 3 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 |
3 | HG02630.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.318+1096delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912450 | |||||||
| chr12:116912451 | C | CT | 13 | a0002c0002t0002g0076 a0002c0002t0002g0077 a0002c0002t0002g0079 others(10): Show |
15 | HG00323.hp1 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.318+1117dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912451 | ||||||
| chr12:116912451 | C | CTT | 13 | a0003c0003t0006g0006 a0003c0003t0006g0009 a0003c0003t0010g0013 others(10): Show |
13 | HG00741.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.318+1116_318+1117d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912451 | ||||||
| chr12:116912451 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.318+1096C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912451 | |||||||
| chr12:116912451 | CT | C | 148 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(145): Show |
149 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.318+1117delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912451 | ||||||
| chr12:116912615 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.318+1260C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912615 | |||||||
| chr12:116912664 | T | C | 1 | a0009c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.318+1309T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912664 | |||||||
| chr12:116912714 | C | T | 155 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.318+1359C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912714 | |||||||
| chr12:116912724 | A | G | 1 | a0002c0002t0011g0147 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.318+1369A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912724 | |||||||
| chr12:116912755 | G | T | 3 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0007c0012t0018g0012 |
3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.318+1400G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912755 | |||||||
| chr12:116912777 | T | A | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+1422T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912777 | |||||||
| chr12:116912778 | A | C | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+1423A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912778 | |||||||
| chr12:116913020 | G | A | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+1665G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913020 | |||||||
| chr12:116913118 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318+1763C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913118 | |||||||
| chr12:116913170 | T | C | 22 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+1815T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913170 | |||||||
| chr12:116913180 | C | CA | 22 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+1827dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116913180 | ||||||
| chr12:116913458 | T | C | 1 | a0002c0002t0002g0053 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.318+2103T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913458 | |||||||
| chr12:116913722 | C | G | 1 | a0002c0002t0001g0146 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.318+2367C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913722 | |||||||
| chr12:116913744 | G | A | 1 | a0003c0005t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.318+2389G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913744 | |||||||
| chr12:116913769 | T | C | 22 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+2414T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913769 | |||||||
| chr12:116913828 | G | C | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2473G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913828 | |||||||
| chr12:116913830 | A | C | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2475A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913830 | |||||||
| chr12:116913832 | C | A | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2477C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913832 | |||||||
| chr12:116913833 | T | G | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2478T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913833 | |||||||
| chr12:116913836 | T | G | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2481T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913836 | |||||||
| chr12:116913838 | C | G | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2483C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913838 | |||||||
| chr12:116913839 | A | T | 1 | a0004c0004t0001g0160 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2484A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913839 | |||||||
| chr12:116914034 | G | A | 22 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+2679G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914034 | |||||||
| chr12:116914293 | T | C | 6 | a0003c0005t0002g0054 a0003c0005t0002g0055 a0003c0005t0002g0056 others(3): Show |
6 | HG02257.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+2938T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914293 | |||||||
| chr12:116914342 | G | A | 7 | a0003c0003t0019g0024 a0005c0007t0002g0026 a0005c0007t0007g0002 others(4): Show |
8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+2987G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914342 | |||||||
| chr12:116914484 | G | A | 2 | a0001c0001t0014g0161 a0001c0001t0014g0162 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.318+3129G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914484 | |||||||
| chr12:116914542 | C | T | 7 | a0003c0003t0019g0024 a0005c0007t0002g0026 a0005c0007t0007g0002 others(4): Show |
8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+3187C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914542 | |||||||
| chr12:116914572 | C | CA | 139 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0164 others(136): Show |
142 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.318+3238dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116914572 | ||||||
| chr12:116914572 | C | CAA | 43 | a0001c0001t0001g0159 a0001c0001t0001g0169 a0001c0001t0001g0170 others(40): Show |
43 | HG00544.hp2 HG00642.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.318+3237_318+3238d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116914572 | ||||||
| chr12:116914572 | C | CAAA | 8 | a0001c0001t0003g0163 a0001c0001t0004g0031 a0001c0001t0004g0032 others(5): Show |
8 | HG00544.hp1 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+3236_318+3238d others(5): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116914572 | ||||||
| chr12:116914594 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318+3239G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914594 | |||||||
| chr12:116914752 | G | A | 155 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.318+3397G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914752 | |||||||
| chr12:116914779 | G | T | 7 | a0003c0003t0019g0024 a0005c0007t0002g0026 a0005c0007t0007g0002 others(4): Show |
8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+3424G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914779 | |||||||
| chr12:116915041 | A | G | 1 | a0002c0002t0002g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.318+3686A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915041 | |||||||
| chr12:116915105 | C | T | 1 | a0004c0004t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.318+3750C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915105 | |||||||
| chr12:116915214 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.318+3859G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915214 | |||||||
| chr12:116915432 | A | G | 162 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(159): Show |
163 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.318+4077A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915432 | |||||||
| chr12:116915640 | C | CT | 42 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(39): Show |
43 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.318+4313dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915640 | C | CTT | 18 | a0002c0002t0002g0076 a0002c0002t0002g0077 a0002c0002t0002g0079 others(15): Show |
18 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.318+4312_318+4313d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915640 | C | CTTT | 7 | a0003c0003t0006g0008 a0003c0003t0006g0009 a0003c0005t0002g0054 others(4): Show |
7 | HG02257.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+4311_318+4313d others(5): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915640 | CTTTT | C | 10 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0188 others(7): Show |
10 | HG01261.hp2 HG02135.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.318+4310_318+4313d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915640 | CTTTTT | C | 77 | a0001c0001t0001g0048 a0001c0001t0001g0159 a0001c0001t0001g0164 others(74): Show |
77 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.318+4309_318+4313d others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915640 | CTTTTTT | C | 20 | a0001c0001t0001g0157 a0001c0001t0001g0169 a0001c0001t0001g0170 others(17): Show |
20 | HG00423.hp1 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.318+4308_318+4313d others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915640 | CTTTTTTT | C | 55 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(52): Show |
56 | HG00140.hp2 HG00544.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.318+4307_318+4313d others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915640 | CTTTTTTT others(5): Show |
C | 1 | a0003c0003t0012g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.318+4302_318+4313d others(14): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915640 | CTTTTTTT others(9): Show |
C | 1 | a0002c0002t0002g0080 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.318+4298_318+4313d others(18): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | ||||||
| chr12:116915675 | T | TA | 22 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+4321dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915675 | ||||||
| chr12:116915689 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.318+4334G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915689 | |||||||
| chr12:116915737 | T | C | 22 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+4382T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915737 | |||||||
| chr12:116915911 | G | A | 197 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(194): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.318+4556G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915911 | |||||||
| chr12:116916099 | A | C | 7 | a0003c0003t0019g0024 a0005c0007t0002g0026 a0005c0007t0007g0002 others(4): Show |
8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+4744A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916099 | |||||||
| chr12:116916229 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG00323.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.318+4874G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916229 | |||||||
| chr12:116916288 | A | T | 1 | a0002c0002t0016g0112 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.318+4933A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916288 | |||||||
| chr12:116916462 | G | C | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.318+5107G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916462 | |||||||
| chr12:116916534 | G | T | 1 | a0003c0003t0001g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.318+5179G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916534 | |||||||
| chr12:116916627 | G | C | 16 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(13): Show |
16 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+5272G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916627 | |||||||
| chr12:116916630 | G | C | 1 | a0001c0001t0004g0038 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.318+5275G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916630 | |||||||
| chr12:116916889 | C | CGT | 8 | a0001c0001t0001g0174 a0002c0002t0002g0079 a0002c0002t0002g0144 others(5): Show |
8 | HG02257.hp2 HG02922.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+5556_318+5557d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916889 | ||||||
| chr12:116916889 | C | T | 1 | a0003c0003t0006g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.318+5534C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916889 | |||||||
| chr12:116916889 | CGT | C | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.318+5556_318+5557d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916889 | ||||||
| chr12:116916907 | T | TGA | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.318+5553_318+5554i others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916907 | ||||||
| chr12:116916909 | T | A | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.318+5554T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916909 | |||||||
| chr12:116916909 | T | TGA | 10 | a0003c0003t0010g0017 a0003c0003t0010g0019 a0003c0003t0019g0024 others(7): Show |
11 | HG00741.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.318+5555_318+5556i others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916909 | ||||||
| chr12:116916911 | T | A | 25 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(22): Show |
27 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.318+5556T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916911 | |||||||
| chr12:116916911 | T | TGAGA | 54 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(51): Show |
54 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.318+5569_318+5572d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | ||||||
| chr12:116916911 | T | TGTGA | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.318+5557_318+5558i others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | ||||||
| chr12:116916911 | T | TGTGAGAG others(1): Show |
14 | a0001c0001t0001g0048 a0001c0001t0001g0171 a0001c0001t0001g0173 others(11): Show |
14 | HG00621.hp1 HG02071.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+5557_318+5558i others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | ||||||
| chr12:116916911 | T | TGTGTGAG others(1): Show |
75 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0169 others(72): Show |
75 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.318+5557_318+5558i others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | ||||||
| chr12:116916911 | T | TGTGTGTG others(3): Show |
9 | a0001c0001t0001g0159 a0001c0001t0001g0189 a0001c0001t0001g0225 others(6): Show |
9 | HG00323.hp2 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+5557_318+5558i others(12): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | ||||||
| chr12:116916913 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.318+5558A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916913 | |||||||
| chr12:116916954 | C | T | 1 | a0003c0003t0010g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.318+5599C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916954 | |||||||
| chr12:116916980 | C | T | 165 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(162): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.318+5625C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916980 | |||||||
| chr12:116917128 | A | G | 1 | a0001c0001t0003g0212 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.318+5773A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917128 | |||||||
| chr12:116917405 | C | T | 4 | a0003c0003t0010g0016 a0003c0003t0021g0007 a0003c0021t0017g0005 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+6050C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917405 | |||||||
| chr12:116917662 | G | A | 4 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+6307G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917662 | |||||||
| chr12:116917751 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.318+6396G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917751 | |||||||
| chr12:116917863 | G | A | 2 | a0003c0003t0010g0013 a0003c0003t0010g0014 |
2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.318+6508G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917863 | |||||||
| chr12:116917890 | G | T | 1 | a0002c0002t0002g0139 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.318+6535G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917890 | |||||||
| chr12:116917991 | C | CA | 146 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.318+6649dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116917991 | ||||||
| chr12:116918005 | C | A | 3 | a0001c0001t0001g0231 a0002c0002t0028g0063 a0003c0021t0017g0005 |
3 | HG02132.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.318+6650C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918005 | |||||||
| chr12:116918013 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.318+6658A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918013 | |||||||
| chr12:116918231 | C | A | 3 | a0002c0002t0002g0086 a0002c0002t0002g0087 a0002c0002t0002g0088 |
3 | HG02486.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.318+6876C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918231 | |||||||
| chr12:116918474 | G | A | 7 | a0003c0003t0019g0024 a0005c0007t0002g0026 a0005c0007t0007g0002 others(4): Show |
8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+7119G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918474 | |||||||
| chr12:116918508 | C | T | 1 | a0002c0002t0008g0111 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.318+7153C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918508 | |||||||
| chr12:116918535 | G | T | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+7180G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918535 | |||||||
| chr12:116918580 | A | C | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.318+7225A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918580 | |||||||
| chr12:116918739 | C | G | 1 | a0002c0002t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.318+7384C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918739 | |||||||
| chr12:116918787 | T | G | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.318+7432T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918787 | |||||||
| chr12:116918799 | A | G | 1 | a0002c0008t0002g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.318+7444A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918799 | |||||||
| chr12:116918963 | A | G | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.318+7608A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918963 | |||||||
| chr12:116918965 | G | GT | 7 | a0002c0002t0005g0064 a0002c0002t0008g0069 a0002c0002t0008g0083 others(4): Show |
7 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+7619dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116918965 | ||||||
| chr12:116919054 | A | G | 1 | a0002c0008t0002g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.318+7699A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116919054 | |||||||
| chr12:116919640 | G | A | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.318+8285G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116919640 | |||||||
| chr12:116919686 | GT | G | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.318+8334delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116919686 | ||||||
| chr12:116919819 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.319-8204A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116919819 | |||||||
| chr12:116920128 | G | A | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.319-7895G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920128 | |||||||
| chr12:116920177 | T | C | 1 | a0001c0001t0003g0194 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.319-7846T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920177 | |||||||
| chr12:116920223 | G | T | 2 | a0001c0006t0001g0271 a0001c0006t0001g0284 |
2 | HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.319-7800G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920223 | |||||||
| chr12:116920402 | G | C | 1 | a0001c0001t0025g0273 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.319-7621G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920402 | |||||||
| chr12:116920412 | A | G | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.319-7611A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920412 | |||||||
| chr12:116920485 | T | G | 1 | a0001c0001t0001g0274 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.319-7538T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920485 | |||||||
| chr12:116920576 | T | A | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-7447T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920576 | |||||||
| chr12:116920619 | C | T | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-7404C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920619 | |||||||
| chr12:116920698 | G | C | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-7325G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920698 | |||||||
| chr12:116920714 | G | A | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-7309G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920714 | |||||||
| chr12:116920720 | A | G | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.319-7303A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920720 | |||||||
| chr12:116921139 | G | A | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-6884G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921139 | |||||||
| chr12:116921227 | A | G | 2 | a0001c0006t0001g0183 a0001c0006t0001g0270 |
2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.319-6796A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921227 | |||||||
| chr12:116921278 | G | A | 1 | a0009c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.319-6745G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921278 | |||||||
| chr12:116921399 | G | A | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.319-6624G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921399 | |||||||
| chr12:116921586 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.319-6437T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921586 | |||||||
| chr12:116921631 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.319-6392C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921631 | |||||||
| chr12:116921692 | G | T | 1 | a0001c0001t0001g0278 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.319-6331G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921692 | |||||||
| chr12:116921710 | T | C | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-6313T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921710 | |||||||
| chr12:116921822 | C | CT | 53 | a0001c0001t0001g0157 a0001c0001t0001g0169 a0001c0001t0001g0181 others(50): Show |
56 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.319-6177dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116921822 | ||||||
| chr12:116921822 | CT | C | 22 | a0001c0001t0001g0184 a0001c0001t0001g0215 a0001c0001t0001g0275 others(19): Show |
23 | HG01433.hp1 HG01884.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.319-6177delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116921822 | ||||||
| chr12:116921822 | CTT | C | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-6178_319-6177d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116921822 | ||||||
| chr12:116922654 | T | G | 1 | a0001c0001t0004g0038 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.319-5369T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922654 | |||||||
| chr12:116922810 | G | GT | 9 | a0001c0001t0003g0212 a0001c0009t0001g0187 a0003c0003t0006g0009 others(6): Show |
10 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-5212dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116922810 | ||||||
| chr12:116922812 | G | GT | 4 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0279 others(1): Show |
4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.319-5203dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116922812 | ||||||
| chr12:116922812 | G | T | 183 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(180): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.319-5211G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922812 | |||||||
| chr12:116922814 | T | G | 5 | a0002c0002t0002g0003 a0002c0002t0002g0089 a0002c0002t0002g0090 others(2): Show |
6 | HG01175.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-5209T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922814 | |||||||
| chr12:116922835 | A | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-5188A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922835 | |||||||
| chr12:116922861 | T | C | 3 | a0002c0002t0005g0092 a0002c0002t0005g0107 a0002c0002t0016g0112 |
3 | NA18975.hp1 NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.319-5162T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922861 | |||||||
| chr12:116922874 | T | G | 232 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(229): Show |
234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.319-5149T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922874 | |||||||
| chr12:116922892 | T | C | 1 | a0003c0003t0021g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.319-5131T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922892 | |||||||
| chr12:116922935 | G | A | 2 | a0001c0001t0003g0148 a0009c0016t0003g0029 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-5088G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922935 | |||||||
| chr12:116923153 | C | G | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.319-4870C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923153 | |||||||
| chr12:116923261 | G | T | 2 | a0001c0001t0004g0037 a0001c0001t0004g0045 |
2 | NA18947.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.319-4762G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923261 | |||||||
| chr12:116923276 | A | AT | 13 | a0001c0001t0001g0275 a0001c0001t0001g0277 a0002c0002t0002g0086 others(10): Show |
14 | HG01884.hp1 HG02083.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.319-4736dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116923276 | ||||||
| chr12:116923287 | TA | T | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-4733delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116923287 | ||||||
| chr12:116923288 | A | T | 146 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(143): Show |
147 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.319-4735A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923288 | |||||||
| chr12:116923517 | T | G | 1 | a0002c0002t0008g0111 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.319-4506T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923517 | |||||||
| chr12:116923542 | CAG | C | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-4478_319-4477d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116923542 | ||||||
| chr12:116923551 | G | T | 1 | a0001c0001t0003g0052 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.319-4472G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923551 | |||||||
| chr12:116923717 | A | T | 12 | a0001c0001t0001g0266 a0002c0002t0002g0091 a0002c0002t0002g0131 others(9): Show |
12 | HG00609.hp1 HG01261.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.319-4306A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923717 | |||||||
| chr12:116923717 | AATTT | A | 6 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0003c0003t0006g0006 others(3): Show |
6 | HG02615.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-4289_319-4286d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116923717 | ||||||
| chr12:116923721 | T | A | 79 | a0001c0001t0001g0159 a0001c0001t0001g0216 a0001c0001t0001g0217 others(76): Show |
80 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.319-4302T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923721 | |||||||
| chr12:116923725 | T | A | 10 | a0002c0002t0011g0082 a0002c0002t0011g0147 a0003c0003t0003g0192 others(7): Show |
10 | HG00741.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-4298T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923725 | |||||||
| chr12:116923729 | T | A | 5 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(2): Show |
5 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-4294T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923729 | |||||||
| chr12:116923796 | C | G | 1 | a0001c0001t0001g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.319-4227C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923796 | |||||||
| chr12:116923936 | A | G | 1 | a0002c0002t0002g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.319-4087A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923936 | |||||||
| chr12:116924117 | C | G | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3906C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924117 | |||||||
| chr12:116924143 | A | C | 184 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(181): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.319-3880A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924143 | |||||||
| chr12:116924146 | GGTTGTCC others(22): Show |
G | 161 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(158): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.319-3845_319-3817d others(31): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116924146 | ||||||
| chr12:116924210 | G | A | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3813G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924210 | |||||||
| chr12:116924285 | C | CTTTTA | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-3735_319-3734i others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116924285 | ||||||
| chr12:116924340 | G | A | 1 | a0002c0002t0002g0114 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.319-3683G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924340 | |||||||
| chr12:116924407 | G | A | 184 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(181): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.319-3616G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924407 | |||||||
| chr12:116924574 | T | C | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-3449T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924574 | |||||||
| chr12:116924648 | G | A | 181 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(178): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.319-3375G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924648 | |||||||
| chr12:116924864 | C | T | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-3159C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924864 | |||||||
| chr12:116924893 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.319-3130A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924893 | |||||||
| chr12:116925076 | TA | T | 6 | a0003c0003t0010g0016 a0003c0003t0010g0017 a0003c0003t0010g0019 others(3): Show |
6 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-2935delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116925076 | ||||||
| chr12:116925137 | G | A | 1 | a0003c0005t0002g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319-2886G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925137 | |||||||
| chr12:116925239 | T | G | 184 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(181): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.319-2784T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925239 | |||||||
| chr12:116925245 | G | A | 158 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(155): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.319-2778G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925245 | |||||||
| chr12:116925361 | G | T | 133 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.319-2662G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925361 | |||||||
| chr12:116925398 | G | A | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-2625G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925398 | |||||||
| chr12:116925502 | G | C | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.319-2521G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925502 | |||||||
| chr12:116925640 | G | A | 2 | a0002c0002t0011g0082 a0002c0002t0011g0147 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.319-2383G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925640 | |||||||
| chr12:116925652 | T | A | 152 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.319-2371T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925652 | |||||||
| chr12:116925693 | A | G | 1 | a0002c0008t0002g0067 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.319-2330A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925693 | |||||||
| chr12:116925775 | C | A | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-2248C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925775 | |||||||
| chr12:116925903 | GTA | G | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319-2118_319-2117d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116925903 | ||||||
| chr12:116925929 | C | T | 1 | a0002c0008t0002g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.319-2094C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925929 | |||||||
| chr12:116926007 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.319-2016G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926007 | |||||||
| chr12:116926026 | A | G | 154 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.319-1997A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926026 | |||||||
| chr12:116926050 | G | A | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.319-1973G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926050 | |||||||
| chr12:116926474 | G | T | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.319-1549G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926474 | |||||||
| chr12:116926630 | C | G | 5 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(2): Show |
5 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-1393C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926630 | |||||||
| chr12:116926760 | T | A | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-1263T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926760 | |||||||
| chr12:116926845 | C | A | 2 | a0001c0006t0001g0183 a0001c0006t0001g0270 |
2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.319-1178C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926845 | |||||||
| chr12:116926895 | T | C | 160 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(157): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.319-1128T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926895 | |||||||
| chr12:116927025 | G | A | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-998G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927025 | |||||||
| chr12:116927174 | A | G | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-849A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927174 | |||||||
| chr12:116927701 | G | A | 232 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(229): Show |
234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.319-322G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927701 | |||||||
| chr12:116927960 | G | A | 1 | a0001c0001t0003g0205 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.319-63G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927960 | |||||||
| chr12:116928004 | CTT | C | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-10_319-9delTT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116928004 | ||||||
| chr12:116928195 | G | A | 2 | a0001c0001t0003g0148 a0002c0002t0002g0095 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.423+68G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928195 | |||||||
| chr12:116928416 | A | G | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+289A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928416 | |||||||
| chr12:116928494 | A | G | 238 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(235): Show |
242 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.423+367A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928494 | |||||||
| chr12:116928500 | T | G | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+373T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928500 | |||||||
| chr12:116928533 | C | A | 152 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.423+406C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928533 | |||||||
| chr12:116928589 | T | C | 19 | a0001c0001t0003g0163 a0001c0001t0003g0191 a0001c0001t0003g0197 others(16): Show |
19 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.423+462T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928589 | |||||||
| chr12:116928664 | G | A | 3 | a0002c0002t0005g0092 a0002c0002t0005g0107 a0002c0002t0016g0112 |
3 | NA18975.hp1 NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.423+537G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928664 | |||||||
| chr12:116928726 | C | T | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+599C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928726 | |||||||
| chr12:116928976 | A | G | 1 | a0001c0001t0004g0036 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.423+849A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928976 | |||||||
| chr12:116929017 | C | G | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+890C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929017 | |||||||
| chr12:116929084 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.423+957G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929084 | |||||||
| chr12:116929116 | T | A | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+989T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929116 | |||||||
| chr12:116929216 | G | A | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+1089G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929216 | |||||||
| chr12:116929303 | C | T | 1 | a0003c0003t0006g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.423+1176C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929303 | |||||||
| chr12:116929425 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+1298C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929425 | |||||||
| chr12:116929494 | C | T | 3 | a0001c0001t0003g0202 a0001c0001t0003g0203 a0001c0001t0003g0214 |
3 | HG01168.hp2 HG01169.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.423+1367C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929494 | |||||||
| chr12:116929517 | G | T | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.423+1390G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929517 | |||||||
| chr12:116929543 | CT | C | 232 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(229): Show |
234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.423+1423delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116929543 | ||||||
| chr12:116929591 | A | G | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.423+1464A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929591 | |||||||
| chr12:116929679 | C | T | 1 | a0002c0002t0002g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.423+1552C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929679 | |||||||
| chr12:116929813 | T | C | 3 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0007c0012t0018g0012 |
3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423+1686T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929813 | |||||||
| chr12:116930621 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.423+2494C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116930621 | |||||||
| chr12:116930753 | C | T | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.423+2626C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116930753 | |||||||
| chr12:116930814 | A | C | 1 | a0007c0012t0018g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.423+2687A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116930814 | |||||||
| chr12:116930855 | T | C | 126 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(123): Show |
127 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.423+2728T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116930855 | |||||||
| chr12:116931011 | T | C | 2 | a0001c0001t0003g0148 a0009c0016t0003g0029 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.423+2884T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931011 | |||||||
| chr12:116931028 | G | A | 1 | a0002c0002t0008g0111 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.423+2901G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931028 | |||||||
| chr12:116931079 | G | T | 5 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(2): Show |
5 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+2952G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931079 | |||||||
| chr12:116931123 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+2996C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931123 | |||||||
| chr12:116931458 | C | CT | 4 | a0002c0002t0002g0129 a0002c0002t0002g0138 a0002c0011t0002g0130 others(1): Show |
4 | NA18956.hp1 NA18965.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+3334dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116931458 | ||||||
| chr12:116931480 | G | A | 5 | a0001c0006t0001g0183 a0001c0006t0001g0245 a0001c0006t0001g0270 others(2): Show |
5 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+3353G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931480 | |||||||
| chr12:116931536 | C | T | 133 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.423+3409C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931536 | |||||||
| chr12:116931640 | G | A | 236 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(233): Show |
240 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.423+3513G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931640 | |||||||
| chr12:116931667 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.423+3540A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931667 | |||||||
| chr12:116931943 | C | G | 4 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0279 others(1): Show |
4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+3816C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931943 | |||||||
| chr12:116931998 | G | C | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423+3871G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931998 | |||||||
| chr12:116932163 | G | T | 4 | a0002c0002t0002g0104 a0002c0002t0002g0105 a0002c0002t0002g0106 others(1): Show |
4 | HG01891.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+4036G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932163 | |||||||
| chr12:116932174 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.423+4047G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932174 | |||||||
| chr12:116932277 | A | G | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.423+4150A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932277 | |||||||
| chr12:116932430 | T | C | 1 | a0003c0003t0006g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.423+4303T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932430 | |||||||
| chr12:116932598 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+4471C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932598 | |||||||
| chr12:116932605 | G | A | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+4478G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932605 | |||||||
| chr12:116932610 | A | G | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+4483A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932610 | |||||||
| chr12:116932637 | G | A | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.423+4510G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932637 | |||||||
| chr12:116932766 | T | G | 8 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(5): Show |
9 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+4639T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932766 | |||||||
| chr12:116932783 | C | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+4656C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932783 | |||||||
| chr12:116932852 | A | G | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+4725A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932852 | |||||||
| chr12:116933021 | T | TA | 59 | a0001c0001t0001g0180 a0001c0001t0001g0264 a0001c0001t0001g0265 others(56): Show |
59 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.423+4902dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116933021 | ||||||
| chr12:116933021 | T | TAA | 95 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(92): Show |
95 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.423+4901_423+4902d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116933021 | ||||||
| chr12:116933021 | TA | T | 10 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(7): Show |
13 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.423+4902delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116933021 | ||||||
| chr12:116933149 | C | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+5022C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933149 | |||||||
| chr12:116933166 | C | T | 1 | a0003c0005t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.423+5039C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933166 | |||||||
| chr12:116933169 | G | C | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+5042G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933169 | |||||||
| chr12:116933282 | A | G | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.423+5155A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933282 | |||||||
| chr12:116933669 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.423+5542G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933669 | |||||||
| chr12:116933713 | A | T | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+5586A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933713 | |||||||
| chr12:116933774 | C | A | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.423+5647C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933774 | |||||||
| chr12:116933961 | T | C | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+5834T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933961 | |||||||
| chr12:116934012 | A | T | 30 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(27): Show |
30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.423+5885A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934012 | |||||||
| chr12:116934178 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.423+6051C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934178 | |||||||
| chr12:116934301 | G | A | 1 | a0002c0002t0002g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.423+6174G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934301 | |||||||
| chr12:116934315 | C | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.423+6188C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934315 | |||||||
| chr12:116934321 | G | A | 1 | a0003c0003t0006g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.423+6194G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934321 | |||||||
| chr12:116934401 | A | T | 2 | a0003c0003t0010g0013 a0003c0003t0010g0014 |
2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.423+6274A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934401 | |||||||
| chr12:116934438 | CT | C | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.423+6318delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116934438 | ||||||
| chr12:116934575 | A | C | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.423+6448A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934575 | |||||||
| chr12:116934889 | G | A | 6 | a0001c0006t0001g0183 a0001c0006t0001g0224 a0001c0006t0001g0245 others(3): Show |
6 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+6762G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934889 | |||||||
| chr12:116934955 | CCTTT | C | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.423+6830_423+6833d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116934955 | ||||||
| chr12:116935032 | T | C | 3 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0007c0012t0018g0012 |
3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423+6905T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935032 | |||||||
| chr12:116935033 | T | C | 1 | a0002c0002t0002g0135 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.423+6906T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935033 | |||||||
| chr12:116935249 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.423+7122T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935249 | |||||||
| chr12:116935785 | A | G | 39 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(36): Show |
39 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.423+7658A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935785 | |||||||
| chr12:116935789 | C | T | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.423+7662C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935789 | |||||||
| chr12:116935813 | G | A | 183 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(180): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.423+7686G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935813 | |||||||
| chr12:116935843 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.423+7716G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935843 | |||||||
| chr12:116935851 | G | T | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.423+7724G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935851 | |||||||
| chr12:116935892 | A | T | 2 | a0002c0002t0002g0079 a0002c0002t0002g0144 |
2 | NA18963.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.423+7765A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935892 | |||||||
| chr12:116935926 | G | A | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+7799G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935926 | |||||||
| chr12:116935934 | A | C | 2 | a0003c0003t0010g0016 a0008c0018t0002g0015 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.423+7807A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935934 | |||||||
| chr12:116935953 | T | C | 99 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.423+7826T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935953 | |||||||
| chr12:116936031 | GTA | G | 273 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(270): Show |
278 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.423+7909_423+7910d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116936031 | ||||||
| chr12:116936354 | A | G | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423+8227A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936354 | |||||||
| chr12:116936470 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.423+8343T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936470 | |||||||
| chr12:116936492 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.423+8365C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936492 | |||||||
| chr12:116936518 | G | A | 160 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(157): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.423+8391G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936518 | |||||||
| chr12:116936563 | G | A | 3 | a0005c0007t0007g0002 a0005c0007t0007g0023 a0005c0007t0007g0028 |
4 | HG02145.hp2 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+8436G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936563 | |||||||
| chr12:116936677 | C | T | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.423+8550C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936677 | |||||||
| chr12:116936690 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+8563C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936690 | |||||||
| chr12:116936703 | G | A | 154 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.423+8576G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936703 | |||||||
| chr12:116936829 | G | A | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-8535G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936829 | |||||||
| chr12:116936990 | G | C | 1 | a0002c0002t0026g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.424-8374G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936990 | |||||||
| chr12:116937166 | C | A | 2 | a0003c0003t0010g0016 a0008c0018t0002g0015 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.424-8198C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937166 | |||||||
| chr12:116937386 | C | T | 1 | a0001c0001t0004g0036 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.424-7978C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937386 | |||||||
| chr12:116937413 | G | A | 1 | a0001c0009t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.424-7951G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937413 | |||||||
| chr12:116937469 | A | G | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-7895A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937469 | |||||||
| chr12:116937675 | T | A | 2 | a0001c0001t0003g0163 a0011c0015t0003g0196 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.424-7689T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937675 | |||||||
| chr12:116937700 | G | A | 2 | a0001c0001t0003g0148 a0009c0016t0003g0029 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424-7664G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937700 | |||||||
| chr12:116937720 | CTA | C | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.424-7642_424-7641d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116937720 | ||||||
| chr12:116937732 | T | TCCTC | 22 | a0001c0001t0003g0190 a0002c0002t0011g0082 a0002c0002t0011g0147 others(19): Show |
23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.424-7629_424-7626d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116937732 | ||||||
| chr12:116937853 | C | CT | 160 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(157): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.424-7499dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116937853 | ||||||
| chr12:116938025 | C | A | 2 | a0001c0001t0003g0191 a0001c0001t0003g0230 |
2 | NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.424-7339C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116938025 | |||||||
| chr12:116938612 | T | G | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-6752T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116938612 | |||||||
| chr12:116938856 | G | A | 1 | a0009c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.424-6508G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116938856 | |||||||
| chr12:116938974 | G | C | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-6390G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116938974 | |||||||
| chr12:116939167 | A | G | 4 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-6197A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939167 | |||||||
| chr12:116939293 | T | C | 1 | a0009c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.424-6071T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939293 | |||||||
| chr12:116939299 | C | T | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.424-6065C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939299 | |||||||
| chr12:116939300 | G | A | 1 | a0007c0012t0018g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.424-6064G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939300 | |||||||
| chr12:116939466 | T | C | 1 | a0001c0001t0014g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.424-5898T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939466 | |||||||
| chr12:116940030 | G | A | 2 | a0003c0003t0006g0006 a0003c0003t0006g0008 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424-5334G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940030 | |||||||
| chr12:116940192 | G | C | 1 | a0001c0001t0001g0237 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424-5172G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940192 | |||||||
| chr12:116940255 | C | CT | 27 | a0001c0001t0001g0223 a0001c0001t0003g0199 a0001c0001t0003g0200 others(24): Show |
28 | HG00423.hp1 HG00741.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.424-5096dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116940255 | ||||||
| chr12:116940269 | A | T | 1 | a0001c0001t0003g0201 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.424-5095A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940269 | |||||||
| chr12:116940408 | C | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-4956C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940408 | |||||||
| chr12:116940493 | C | CT | 95 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(92): Show |
95 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.424-4858dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116940493 | ||||||
| chr12:116940506 | T | C | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-4858T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940506 | |||||||
| chr12:116940523 | TA | T | 19 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(16): Show |
19 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.424-4830delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116940523 | ||||||
| chr12:116940607 | A | T | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.424-4757A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940607 | |||||||
| chr12:116940797 | C | T | 1 | a0002c0002t0002g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.424-4567C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940797 | |||||||
| chr12:116940856 | T | C | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424-4508T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940856 | |||||||
| chr12:116940893 | C | T | 1 | a0001c0001t0003g0156 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.424-4471C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940893 | |||||||
| chr12:116941139 | C | T | 11 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(8): Show |
11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.424-4225C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941139 | |||||||
| chr12:116941245 | G | A | 1 | a0002c0008t0002g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424-4119G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941245 | |||||||
| chr12:116941293 | T | C | 1 | a0002c0002t0002g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.424-4071T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941293 | |||||||
| chr12:116941320 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424-4044G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941320 | |||||||
| chr12:116941368 | A | G | 2 | a0003c0003t0010g0016 a0008c0018t0002g0015 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.424-3996A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941368 | |||||||
| chr12:116941880 | C | G | 7 | a0001c0001t0001g0164 a0001c0001t0001g0215 a0001c0001t0001g0262 others(4): Show |
7 | HG01192.hp1 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-3484C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941880 | |||||||
| chr12:116942085 | A | G | 23 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(20): Show |
24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.424-3279A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942085 | |||||||
| chr12:116942155 | A | G | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-3209A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942155 | |||||||
| chr12:116942188 | C | A | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.424-3176C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942188 | |||||||
| chr12:116942195 | A | AT | 16 | a0001c0001t0001g0219 a0001c0001t0015g0261 a0002c0002t0011g0082 others(13): Show |
18 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.424-3155dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942195 | ||||||
| chr12:116942233 | A | C | 3 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 |
3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.424-3131A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942233 | |||||||
| chr12:116942351 | A | G | 1 | a0003c0003t0011g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.424-3013A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942351 | |||||||
| chr12:116942374 | A | AT | 169 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(166): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.424-2974dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942374 | ||||||
| chr12:116942374 | A | ATT | 16 | a0001c0001t0001g0176 a0001c0001t0001g0219 a0003c0003t0010g0013 others(13): Show |
17 | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.424-2975_424-2974d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942374 | ||||||
| chr12:116942770 | A | AT | 43 | a0002c0002t0001g0146 a0002c0002t0002g0030 a0002c0002t0002g0072 others(40): Show |
44 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.424-2569dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942770 | ||||||
| chr12:116942770 | A | ATT | 12 | a0002c0002t0002g0139 a0002c0002t0002g0141 a0002c0002t0002g0143 others(9): Show |
14 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.424-2570_424-2569d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942770 | ||||||
| chr12:116942770 | AT | A | 64 | a0001c0001t0001g0169 a0001c0001t0001g0182 a0001c0001t0001g0222 others(61): Show |
64 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.424-2569delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942770 | ||||||
| chr12:116942770 | ATT | A | 104 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(101): Show |
104 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.424-2570_424-2569d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942770 | ||||||
| chr12:116942800 | C | T | 7 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(4): Show |
7 | HG02486.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-2564C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942800 | |||||||
| chr12:116942864 | G | A | 1 | a0004c0004t0001g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.424-2500G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942864 | |||||||
| chr12:116943156 | G | A | 231 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(228): Show |
233 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.424-2208G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943156 | |||||||
| chr12:116943228 | T | A | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.424-2136T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943228 | |||||||
| chr12:116943255 | C | G | 8 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0003t0012g0020 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-2109C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943255 | |||||||
| chr12:116943320 | T | C | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424-2044T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943320 | |||||||
| chr12:116943564 | T | C | 99 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.424-1800T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943564 | |||||||
| chr12:116943841 | C | T | 2 | a0001c0001t0031g0049 a0001c0001t0032g0046 |
2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.424-1523C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943841 | |||||||
| chr12:116944056 | G | A | 30 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(27): Show |
30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.424-1308G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944056 | |||||||
| chr12:116944241 | G | A | 1 | a0002c0002t0002g0138 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.424-1123G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944241 | |||||||
| chr12:116944309 | C | G | 2 | a0003c0003t0010g0016 a0008c0018t0002g0015 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.424-1055C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944309 | |||||||
| chr12:116944485 | C | T | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.424-879C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944485 | |||||||
| chr12:116944598 | C | T | 1 | a0002c0002t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.424-766C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944598 | |||||||
| chr12:116944599 | G | A | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424-765G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944599 | |||||||
| chr12:116944691 | A | C | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.424-673A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944691 | |||||||
| chr12:116945174 | T | C | 1 | a0002c0002t0026g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.424-190T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116945174 | |||||||
| chr12:116945258 | A | G | 2 | a0002c0002t0002g0127 a0002c0002t0027g0140 |
2 | HG01975.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.424-106A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116945258 | |||||||
| chr12:116945786 | C | G | 1 | a0001c0001t0001g0247 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.588+258C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116945786 | |||||||
| chr12:116945910 | A | G | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.588+382A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116945910 | |||||||
| chr12:116946311 | A | C | 1 | a0002c0002t0002g0126 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.588+783A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946311 | |||||||
| chr12:116946357 | T | C | 30 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(27): Show |
30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.588+829T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946357 | |||||||
| chr12:116946443 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.588+915G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946443 | |||||||
| chr12:116946599 | T | A | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+1071T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946599 | |||||||
| chr12:116946604 | G | C | 153 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.588+1076G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946604 | |||||||
| chr12:116946716 | G | A | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.588+1188G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946716 | |||||||
| chr12:116946773 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.588+1245G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946773 | |||||||
| chr12:116947076 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.588+1548G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947076 | |||||||
| chr12:116947230 | G | C | 89 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(86): Show |
89 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.588+1702G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947230 | |||||||
| chr12:116947273 | T | C | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+1745T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947273 | |||||||
| chr12:116947346 | G | C | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.588+1818G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947346 | |||||||
| chr12:116947360 | A | G | 1 | a0009c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.588+1832A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947360 | |||||||
| chr12:116947362 | T | G | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.588+1834T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947362 | |||||||
| chr12:116947472 | G | A | 2 | a0002c0002t0011g0082 a0002c0002t0011g0147 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.588+1944G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947472 | |||||||
| chr12:116947736 | C | CA | 11 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(8): Show |
11 | HG01106.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.589-1864dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116947736 | ||||||
| chr12:116947750 | A | AAAAAG | 89 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.589-1859_589-1855d others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116947750 | ||||||
| chr12:116947750 | A | AAAAG | 66 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0253 others(63): Show |
67 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.589-1865_589-1864i others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116947750 | ||||||
| chr12:116947750 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.589-1868A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947750 | |||||||
| chr12:116947751 | A | G | 1 | a0002c0002t0002g0125 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.589-1867A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947751 | |||||||
| chr12:116947768 | G | GAA | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1848_589-1847d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116947768 | ||||||
| chr12:116947798 | T | G | 1 | a0002c0002t0001g0146 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.589-1820T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947798 | |||||||
| chr12:116947807 | G | A | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.589-1811G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947807 | |||||||
| chr12:116947863 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-1755C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947863 | |||||||
| chr12:116947882 | G | A | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.589-1736G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947882 | |||||||
| chr12:116948025 | G | A | 39 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(36): Show |
39 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.589-1593G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948025 | |||||||
| chr12:116948037 | T | C | 1 | a0001c0001t0003g0199 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.589-1581T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948037 | |||||||
| chr12:116948233 | A | G | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1385A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948233 | |||||||
| chr12:116948280 | A | C | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.589-1338A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948280 | |||||||
| chr12:116948365 | G | A | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-1253G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948365 | |||||||
| chr12:116949121 | C | T | 2 | a0002c0002t0009g0060 a0002c0002t0009g0062 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.589-497C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116949121 | |||||||
| chr12:116949336 | T | G | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.589-282T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116949336 | |||||||
| chr12:116949338 | T | C | 1 | a0001c0001t0014g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.589-280T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116949338 | |||||||
| chr12:116949614 | G | A | 1 | a0007c0012t0018g0012 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.589-4G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116949614 | |||||||
| chr12:116949765 | A | G | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.677+59A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949765 | |||||||
| chr12:116949840 | A | G | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.677+134A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949840 | |||||||
| chr12:116949881 | G | A | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.677+175G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949881 | |||||||
| chr12:116949881 | G | T | 1 | a0002c0008t0002g0067 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.677+175G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949881 | |||||||
| chr12:116949906 | G | T | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.677+200G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949906 | |||||||
| chr12:116950182 | G | GT | 23 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0052 others(20): Show |
24 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.677+487dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116950182 | ||||||
| chr12:116950182 | GT | G | 5 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+487delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116950182 | ||||||
| chr12:116950558 | T | C | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+852T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950558 | |||||||
| chr12:116950576 | T | C | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+870T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950576 | |||||||
| chr12:116950620 | C | G | 1 | a0001c0001t0031g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.677+914C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950620 | |||||||
| chr12:116950723 | C | T | 1 | a0001c0009t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.677+1017C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950723 | |||||||
| chr12:116950759 | G | A | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.677+1053G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950759 | |||||||
| chr12:116950844 | A | C | 1 | a0002c0011t0002g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1138A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950844 | |||||||
| chr12:116950887 | G | A | 2 | a0001c0001t0003g0230 a0002c0002t0002g0053 |
2 | HG02155.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.677+1181G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950887 | |||||||
| chr12:116950984 | A | G | 1 | a0002c0008t0002g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.677+1278A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950984 | |||||||
| chr12:116951309 | A | C | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+1603A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951309 | |||||||
| chr12:116951322 | G | A | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.677+1616G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951322 | |||||||
| chr12:116951373 | A | G | 5 | a0001c0001t0004g0031 a0001c0001t0004g0033 a0001c0001t0004g0034 others(2): Show |
5 | HG03491.hp2 HG03492.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.677+1667A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951373 | |||||||
| chr12:116951568 | G | T | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.677+1862G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951568 | |||||||
| chr12:116951592 | C | G | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+1886C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951592 | |||||||
| chr12:116951835 | G | A | 1 | a0002c0002t0005g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.677+2129G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951835 | |||||||
| chr12:116951836 | T | C | 1 | a0001c0001t0004g0036 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.677+2130T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951836 | |||||||
| chr12:116951857 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.677+2151C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951857 | |||||||
| chr12:116952140 | T | A | 1 | a0002c0002t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.677+2434T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952140 | |||||||
| chr12:116952174 | T | C | 163 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(160): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.677+2468T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952174 | |||||||
| chr12:116952313 | G | C | 7 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0238 others(4): Show |
7 | HG01109.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+2607G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952313 | |||||||
| chr12:116952327 | C | T | 4 | a0002c0002t0002g0075 a0002c0002t0002g0084 a0002c0002t0002g0141 others(1): Show |
4 | NA18959.hp1 NA18997.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+2621C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952327 | |||||||
| chr12:116952344 | G | A | 99 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.677+2638G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952344 | |||||||
| chr12:116952534 | T | C | 163 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(160): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.677+2828T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952534 | |||||||
| chr12:116952543 | G | A | 2 | a0002c0002t0011g0082 a0002c0002t0011g0147 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.677+2837G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952543 | |||||||
| chr12:116952550 | T | C | 282 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(279): Show |
287 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.677+2844T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952550 | |||||||
| chr12:116952572 | C | T | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.677+2866C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952572 | |||||||
| chr12:116952605 | G | A | 163 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(160): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.677+2899G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952605 | |||||||
| chr12:116952611 | C | T | 1 | a0001c0009t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.677+2905C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952611 | |||||||
| chr12:116952628 | A | G | 2 | a0003c0003t0010g0013 a0003c0003t0010g0014 |
2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.677+2922A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952628 | |||||||
| chr12:116952748 | A | C | 1 | a0001c0001t0004g0041 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.677+3042A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952748 | |||||||
| chr12:116952820 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+3114C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952820 | |||||||
| chr12:116952883 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.677+3177G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952883 | |||||||
| chr12:116953022 | G | A | 5 | a0005c0007t0007g0002 a0005c0007t0007g0023 a0005c0007t0007g0025 others(2): Show |
6 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+3316G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953022 | |||||||
| chr12:116953154 | T | C | 12 | a0002c0002t0002g0072 a0002c0002t0002g0077 a0002c0002t0002g0079 others(9): Show |
12 | HG02071.hp2 HG02738.hp2 NA18954.hp2 others(9): Show |
intron_variant | MODIFIER | c.677+3448T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953154 | |||||||
| chr12:116953378 | C | G | 163 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(160): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.677+3672C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953378 | |||||||
| chr12:116953383 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.677+3677G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953383 | |||||||
| chr12:116953416 | T | G | 1 | a0003c0003t0001g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.677+3710T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953416 | |||||||
| chr12:116953485 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.677+3779C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953485 | |||||||
| chr12:116953500 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.677+3794G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953500 | |||||||
| chr12:116953792 | AC | A | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.677+4087delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953792 | |||||||
| chr12:116953982 | C | T | 10 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(7): Show |
11 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.677+4276C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953982 | |||||||
| chr12:116954111 | CA | C | 181 | a0001c0001t0001g0048 a0001c0001t0001g0159 a0001c0001t0001g0164 others(178): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.677+4428delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116954111 | ||||||
| chr12:116954111 | CAA | C | 18 | a0002c0002t0002g0116 a0002c0002t0002g0131 a0003c0003t0006g0004 others(15): Show |
19 | HG00609.hp1 HG00741.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.677+4427_677+4428d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116954111 | ||||||
| chr12:116954129 | A | G | 3 | a0002c0002t0002g0086 a0002c0002t0002g0087 a0002c0002t0002g0088 |
3 | HG02486.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.677+4423A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954129 | |||||||
| chr12:116954133 | A | AT | 20 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(17): Show |
20 | HG00544.hp1 HG02080.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.677+4427_677+4428i others(3): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954133 | |||||||
| chr12:116954133 | A | T | 216 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(213): Show |
220 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.677+4427A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954133 | |||||||
| chr12:116954300 | G | A | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.677+4594G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954300 | |||||||
| chr12:116954483 | T | C | 1 | a0001c0001t0003g0154 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.677+4777T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954483 | |||||||
| chr12:116954494 | T | A | 2 | a0002c0002t0002g0089 a0002c0002t0002g0091 |
2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.677+4788T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954494 | |||||||
| chr12:116954666 | C | G | 5 | a0002c0002t0002g0075 a0002c0002t0002g0084 a0002c0002t0002g0131 others(2): Show |
5 | HG00609.hp1 NA18959.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.677+4960C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954666 | |||||||
| chr12:116954710 | G | T | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.677+5004G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954710 | |||||||
| chr12:116954887 | C | G | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+5181C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954887 | |||||||
| chr12:116954970 | T | C | 1 | a0002c0002t0002g0093 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.677+5264T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954970 | |||||||
| chr12:116954981 | C | T | 3 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0007c0012t0018g0012 |
3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.677+5275C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954981 | |||||||
| chr12:116955036 | T | TG | 105 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0164 others(102): Show |
105 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.677+5342dupG | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116955036 | ||||||
| chr12:116955036 | T | TGG | 42 | a0001c0001t0001g0159 a0001c0001t0001g0169 a0001c0001t0001g0170 others(39): Show |
42 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.677+5341_677+5342d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116955036 | ||||||
| chr12:116955036 | TGG | T | 33 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(30): Show |
33 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.677+5341_677+5342d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116955036 | ||||||
| chr12:116955039 | G | C | 18 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0086 others(15): Show |
19 | HG01175.hp1 HG01261.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.677+5333G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955039 | |||||||
| chr12:116955041 | G | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+5335G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955041 | |||||||
| chr12:116955048 | G | C | 5 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(2): Show |
6 | HG02723.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+5342G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955048 | |||||||
| chr12:116955049 | C | G | 11 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(8): Show |
11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.677+5343C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955049 | |||||||
| chr12:116955181 | G | T | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.677+5475G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955181 | |||||||
| chr12:116955319 | C | T | 1 | a0009c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.677+5613C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955319 | |||||||
| chr12:116955853 | A | G | 7 | a0001c0001t0003g0197 a0001c0001t0003g0206 a0001c0001t0003g0207 others(4): Show |
7 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.677+6147A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955853 | |||||||
| chr12:116956190 | C | T | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+6484C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956190 | |||||||
| chr12:116956219 | G | A | 175 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(172): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.677+6513G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956219 | |||||||
| chr12:116956281 | C | G | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.677+6575C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956281 | |||||||
| chr12:116956452 | A | G | 1 | a0002c0002t0008g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.677+6746A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956452 | |||||||
| chr12:116956517 | G | C | 4 | a0002c0002t0002g0104 a0002c0002t0002g0105 a0002c0002t0002g0106 others(1): Show |
4 | HG01891.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+6811G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956517 | |||||||
| chr12:116956542 | G | A | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+6836G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956542 | |||||||
| chr12:116956549 | A | C | 2 | a0001c0001t0003g0191 a0001c0001t0003g0230 |
2 | NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.677+6843A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956549 | |||||||
| chr12:116956725 | T | TGGGAGGC others(20): Show |
1 | a0002c0008t0002g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.677+7023_677+7049d others(29): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116956725 | ||||||
| chr12:116957049 | C | A | 8 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0003t0012g0020 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.677+7343C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116957049 | |||||||
| chr12:116957517 | A | G | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-7180A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116957517 | |||||||
| chr12:116957808 | AATTT | A | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.678-6880_678-6877d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116957808 | ||||||
| chr12:116958036 | C | T | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.678-6661C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958036 | |||||||
| chr12:116958149 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.678-6548A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958149 | |||||||
| chr12:116958153 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.678-6544G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958153 | |||||||
| chr12:116958155 | C | A | 1 | a0003c0003t0010g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.678-6542C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958155 | |||||||
| chr12:116958237 | C | T | 30 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(27): Show |
30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.678-6460C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958237 | |||||||
| chr12:116958292 | G | C | 135 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.678-6405G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958292 | |||||||
| chr12:116958307 | A | G | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.678-6390A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958307 | |||||||
| chr12:116958712 | T | G | 1 | a0002c0002t0002g0117 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.678-5985T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958712 | |||||||
| chr12:116958716 | G | A | 1 | a0002c0002t0002g0117 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.678-5981G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958716 | |||||||
| chr12:116958775 | T | C | 1 | a0003c0003t0021g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.678-5922T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958775 | |||||||
| chr12:116958816 | T | C | 1 | a0002c0002t0011g0147 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.678-5881T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958816 | |||||||
| chr12:116958822 | T | G | 99 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.678-5875T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958822 | |||||||
| chr12:116959008 | T | A | 99 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.678-5689T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959008 | |||||||
| chr12:116959017 | C | T | 171 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(168): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.678-5680C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959017 | |||||||
| chr12:116959596 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.678-5101T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959596 | |||||||
| chr12:116959674 | T | G | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.678-5023T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959674 | |||||||
| chr12:116959825 | G | A | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.678-4872G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959825 | |||||||
| chr12:116959845 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.678-4852T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959845 | |||||||
| chr12:116959949 | G | C | 1 | a0001c0001t0004g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.678-4748G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959949 | |||||||
| chr12:116960241 | A | G | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.678-4456A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960241 | |||||||
| chr12:116960245 | A | C | 1 | a0002c0008t0002g0067 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.678-4452A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960245 | |||||||
| chr12:116960250 | G | C | 11 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(8): Show |
11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.678-4447G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960250 | |||||||
| chr12:116960338 | G | A | 6 | a0001c0001t0001g0159 a0001c0001t0001g0189 a0001c0001t0001g0225 others(3): Show |
6 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.678-4359G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960338 | |||||||
| chr12:116960404 | C | T | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-4293C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960404 | |||||||
| chr12:116960576 | G | T | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.678-4121G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960576 | |||||||
| chr12:116960643 | T | C | 165 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(162): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.678-4054T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960643 | |||||||
| chr12:116960848 | A | AT | 5 | a0003c0003t0010g0016 a0003c0003t0010g0017 a0003c0003t0010g0019 others(2): Show |
5 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-3849_678-3848i others(3): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960848 | |||||||
| chr12:116960943 | A | T | 3 | a0002c0002t0002g0030 a0002c0002t0002g0098 a0002c0002t0022g0097 |
3 | HG02630.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.678-3754A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960943 | |||||||
| chr12:116960970 | A | G | 9 | a0001c0001t0001g0264 a0003c0003t0011g0010 a0003c0003t0011g0011 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.678-3727A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960970 | |||||||
| chr12:116961098 | C | T | 8 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0003t0012g0020 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.678-3599C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961098 | |||||||
| chr12:116961117 | TC | T | 3 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0002g0126 |
3 | NA19010.hp2 NA19068.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.678-3577delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116961117 | ||||||
| chr12:116961274 | C | A | 11 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(8): Show |
11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.678-3423C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961274 | |||||||
| chr12:116961325 | A | T | 1 | a0001c0001t0004g0165 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.678-3372A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961325 | |||||||
| chr12:116961437 | G | A | 2 | a0002c0002t0005g0064 a0002c0002t0005g0100 |
2 | HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.678-3260G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961437 | |||||||
| chr12:116961454 | C | T | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.678-3243C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961454 | |||||||
| chr12:116961508 | G | A | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-3189G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961508 | |||||||
| chr12:116961607 | C | A | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.678-3090C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961607 | |||||||
| chr12:116961676 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.678-3021G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961676 | |||||||
| chr12:116961715 | C | G | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.678-2982C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961715 | |||||||
| chr12:116961899 | C | T | 32 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(29): Show |
32 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.678-2798C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961899 | |||||||
| chr12:116962256 | G | A | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.678-2441G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962256 | |||||||
| chr12:116962324 | C | T | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.678-2373C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962324 | |||||||
| chr12:116962565 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.678-2132C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962565 | |||||||
| chr12:116962594 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.678-2103T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962594 | |||||||
| chr12:116962888 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.678-1809C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962888 | |||||||
| chr12:116963014 | C | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.678-1683C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963014 | |||||||
| chr12:116963044 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.678-1653G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963044 | |||||||
| chr12:116963084 | C | T | 1 | a0002c0002t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.678-1613C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963084 | |||||||
| chr12:116963373 | G | A | 2 | a0002c0002t0002g0030 a0002c0002t0022g0097 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.678-1324G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963373 | |||||||
| chr12:116963496 | T | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.678-1201T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963496 | |||||||
| chr12:116963534 | A | C | 2 | a0001c0001t0003g0148 a0009c0016t0003g0029 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.678-1163A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963534 | |||||||
| chr12:116963822 | A | G | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-875A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963822 | |||||||
| chr12:116964496 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.678-201G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116964496 | |||||||
| chr12:116964678 | G | A | 1 | a0001c0001t0025g0273 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.678-19G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116964678 | |||||||
| chr12:116964906 | A | T | 5 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(2): Show |
5 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+52A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116964906 | |||||||
| chr12:116964950 | T | C | 269 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(266): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.835+96T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116964950 | |||||||
| chr12:116965070 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.835+216T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965070 | |||||||
| chr12:116965215 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.835+361A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965215 | |||||||
| chr12:116965224 | T | C | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+370T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965224 | |||||||
| chr12:116965419 | A | T | 1 | a0002c0008t0002g0067 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.835+565A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965419 | |||||||
| chr12:116965535 | TGTGAA | T | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+685_835+689del others(5): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116965535 | ||||||
| chr12:116965629 | C | G | 3 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0007c0012t0018g0012 |
3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.835+775C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965629 | |||||||
| chr12:116965769 | A | G | 2 | a0005c0007t0007g0002 a0005c0007t0007g0023 |
3 | HG02145.hp2 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.835+915A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965769 | |||||||
| chr12:116965904 | G | A | 1 | a0001c0006t0001g0245 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.835+1050G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965904 | |||||||
| chr12:116965925 | A | AT | 62 | a0001c0001t0003g0148 a0001c0001t0003g0195 a0001c0001t0003g0197 others(59): Show |
63 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.835+1090dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116965925 | ||||||
| chr12:116965925 | A | ATT | 157 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(154): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.835+1089_835+1090d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116965925 | ||||||
| chr12:116966092 | A | G | 1 | a0001c0001t0003g0194 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.835+1238A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966092 | |||||||
| chr12:116966133 | C | T | 182 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(179): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.835+1279C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966133 | |||||||
| chr12:116966378 | G | A | 2 | a0002c0002t0005g0064 a0002c0002t0005g0100 |
2 | HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.835+1524G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966378 | |||||||
| chr12:116966417 | G | C | 3 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0007c0012t0018g0012 |
3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.835+1563G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966417 | |||||||
| chr12:116966580 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+1726C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966580 | |||||||
| chr12:116966655 | A | G | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+1801A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966655 | |||||||
| chr12:116966700 | G | A | 4 | a0002c0002t0002g0104 a0002c0002t0002g0105 a0002c0002t0002g0106 others(1): Show |
4 | HG01891.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+1846G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966700 | |||||||
| chr12:116966819 | A | G | 5 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(2): Show |
6 | HG02723.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+1965A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966819 | |||||||
| chr12:116966861 | A | G | 9 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0005c0007t0002g0026 others(6): Show |
10 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.835+2007A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966861 | |||||||
| chr12:116966900 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.835+2046C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966900 | |||||||
| chr12:116966962 | C | A | 171 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(168): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.835+2108C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966962 | |||||||
| chr12:116967138 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.835+2284G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967138 | |||||||
| chr12:116967153 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.835+2299C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967153 | |||||||
| chr12:116967159 | C | CT | 8 | a0001c0001t0003g0051 a0003c0005t0002g0059 a0005c0007t0002g0026 others(5): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+2320dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116967159 | ||||||
| chr12:116967159 | CT | C | 7 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | HG00423.hp2 HG02523.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+2320delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116967159 | ||||||
| chr12:116967593 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.835+2739G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967593 | |||||||
| chr12:116967763 | C | T | 17 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0003c0003t0011g0010 others(14): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.835+2909C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967763 | |||||||
| chr12:116967792 | A | C | 1 | a0004c0004t0001g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.835+2938A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967792 | |||||||
| chr12:116967816 | G | C | 2 | a0001c0001t0014g0161 a0001c0001t0014g0162 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.835+2962G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967816 | |||||||
| chr12:116967850 | T | C | 2 | a0002c0002t0011g0082 a0002c0002t0011g0147 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+2996T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967850 | |||||||
| chr12:116968060 | C | T | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.835+3206C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968060 | |||||||
| chr12:116968065 | G | A | 1 | a0002c0002t0005g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.835+3211G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968065 | |||||||
| chr12:116968131 | AT | A | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+3283delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116968131 | ||||||
| chr12:116968196 | G | C | 156 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.835+3342G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968196 | |||||||
| chr12:116968246 | C | T | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.835+3392C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968246 | |||||||
| chr12:116968282 | T | C | 1 | a0002c0002t0005g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.835+3428T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968282 | |||||||
| chr12:116968464 | G | A | 4 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+3610G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968464 | |||||||
| chr12:116968475 | A | C | 1 | a0002c0002t0002g0139 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.835+3621A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968475 | |||||||
| chr12:116968497 | G | C | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+3643G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968497 | |||||||
| chr12:116968644 | A | G | 1 | a0009c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.835+3790A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968644 | |||||||
| chr12:116968676 | C | G | 1 | a0005c0007t0002g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.835+3822C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968676 | |||||||
| chr12:116969099 | A | G | 1 | a0002c0002t0005g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.835+4245A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969099 | |||||||
| chr12:116969220 | C | A | 1 | a0007c0012t0018g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.835+4366C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969220 | |||||||
| chr12:116969451 | G | A | 1 | a0002c0002t0002g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.835+4597G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969451 | |||||||
| chr12:116969695 | C | T | 153 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.835+4841C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969695 | |||||||
| chr12:116969805 | C | T | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.835+4951C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969805 | |||||||
| chr12:116969840 | AT | A | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+4989delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116969840 | ||||||
| chr12:116970235 | G | A | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.835+5381G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970235 | |||||||
| chr12:116970284 | G | A | 2 | a0002c0002t0011g0082 a0002c0002t0011g0147 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+5430G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970284 | |||||||
| chr12:116970317 | C | T | 8 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0003t0012g0020 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.835+5463C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970317 | |||||||
| chr12:116970320 | G | A | 1 | a0009c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.835+5466G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970320 | |||||||
| chr12:116970343 | T | C | 181 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(178): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.835+5489T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970343 | |||||||
| chr12:116970410 | G | A | 183 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(180): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.835+5556G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970410 | |||||||
| chr12:116970477 | T | C | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.835+5623T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970477 | |||||||
| chr12:116970495 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.835+5641C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970495 | |||||||
| chr12:116970638 | G | A | 160 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(157): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.835+5784G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970638 | |||||||
| chr12:116971053 | A | G | 99 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.835+6199A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971053 | |||||||
| chr12:116971116 | C | T | 32 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(29): Show |
32 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.835+6262C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971116 | |||||||
| chr12:116971326 | T | C | 156 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.835+6472T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971326 | |||||||
| chr12:116971357 | C | CA | 55 | a0001c0001t0001g0164 a0001c0001t0003g0047 a0001c0001t0004g0034 others(52): Show |
55 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.835+6517dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116971357 | ||||||
| chr12:116971845 | G | A | 8 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0003t0012g0020 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.835+6991G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971845 | |||||||
| chr12:116971935 | T | C | 6 | a0001c0006t0001g0183 a0001c0006t0001g0224 a0001c0006t0001g0245 others(3): Show |
6 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+7081T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971935 | |||||||
| chr12:116971947 | A | G | 5 | a0002c0002t0002g0099 a0002c0008t0002g0066 a0002c0008t0002g0067 others(2): Show |
5 | HG01261.hp1 HG02148.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+7093A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971947 | |||||||
| chr12:116972228 | A | G | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+7374A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972228 | |||||||
| chr12:116972354 | G | T | 135 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.835+7500G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972354 | |||||||
| chr12:116972610 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.835+7756C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972610 | |||||||
| chr12:116972630 | G | C | 173 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(170): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.835+7776G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972630 | |||||||
| chr12:116972695 | C | T | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.835+7841C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972695 | |||||||
| chr12:116972830 | G | A | 2 | a0002c0002t0011g0082 a0002c0002t0011g0147 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+7976G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972830 | |||||||
| chr12:116972837 | C | A | 1 | a0001c0001t0003g0156 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.835+7983C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972837 | |||||||
| chr12:116972898 | A | G | 1 | a0001c0001t0004g0036 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835+8044A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972898 | |||||||
| chr12:116973275 | C | T | 99 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.835+8421C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973275 | |||||||
| chr12:116973382 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0052 |
3 | HG02622.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.835+8528C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973382 | |||||||
| chr12:116973483 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.835+8629G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973483 | |||||||
| chr12:116973656 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+8802C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973656 | |||||||
| chr12:116973663 | G | A | 1 | a0004c0004t0001g0255 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.835+8809G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973663 | |||||||
| chr12:116973852 | T | G | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.835+8998T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973852 | |||||||
| chr12:116973861 | C | A | 58 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(55): Show |
58 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.835+9007C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973861 | |||||||
| chr12:116973898 | A | C | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+9044A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973898 | |||||||
| chr12:116974059 | C | T | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.835+9205C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974059 | |||||||
| chr12:116974100 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.835+9246C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974100 | |||||||
| chr12:116974152 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0282 |
3 | HG02818.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.835+9298G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974152 | |||||||
| chr12:116974261 | C | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+9407C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974261 | |||||||
| chr12:116974267 | T | C | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+9413T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974267 | |||||||
| chr12:116974798 | A | G | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.835+9944A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974798 | |||||||
| chr12:116974822 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.835+9968A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974822 | |||||||
| chr12:116975208 | G | A | 2 | a0001c0009t0001g0187 a0001c0009t0001g0246 |
2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.836-9998G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975208 | |||||||
| chr12:116975281 | TTA | T | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.836-9922_836-9921d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116975281 | ||||||
| chr12:116975355 | A | G | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-9851A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975355 | |||||||
| chr12:116975520 | G | C | 2 | a0003c0003t0010g0017 a0003c0003t0010g0019 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.836-9686G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975520 | |||||||
| chr12:116975544 | A | G | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.836-9662A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975544 | |||||||
| chr12:116975545 | A | G | 138 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.836-9661A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975545 | |||||||
| chr12:116975622 | T | C | 13 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(10): Show |
13 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.836-9584T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975622 | |||||||
| chr12:116976153 | C | T | 186 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.836-9053C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976153 | |||||||
| chr12:116976167 | T | C | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.836-9039T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976167 | |||||||
| chr12:116976195 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.836-9011G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976195 | |||||||
| chr12:116976232 | T | C | 6 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(3): Show |
6 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-8974T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976232 | |||||||
| chr12:116976386 | TA | T | 79 | a0001c0001t0001g0278 a0001c0001t0003g0163 a0001c0001t0003g0197 others(76): Show |
80 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.836-8805delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116976386 | ||||||
| chr12:116976450 | C | CT | 31 | a0001c0001t0004g0044 a0002c0002t0002g0030 a0002c0002t0002g0076 others(28): Show |
32 | HG01106.hp1 HG01358.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.836-8734dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116976450 | ||||||
| chr12:116976450 | CT | C | 112 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.836-8734delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116976450 | ||||||
| chr12:116976472 | T | C | 1 | a0003c0003t0006g0009 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.836-8734T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976472 | |||||||
| chr12:116976558 | C | T | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.836-8648C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976558 | |||||||
| chr12:116976621 | AT | A | 166 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(163): Show |
170 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.836-8569delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116976621 | ||||||
| chr12:116976692 | C | T | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.836-8514C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976692 | |||||||
| chr12:116976756 | C | T | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.836-8450C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976756 | |||||||
| chr12:116976779 | T | C | 1 | a0001c0006t0001g0245 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.836-8427T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976779 | |||||||
| chr12:116976894 | C | T | 1 | a0002c0002t0026g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.836-8312C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976894 | |||||||
| chr12:116976985 | C | G | 4 | a0002c0008t0002g0066 a0002c0008t0002g0067 a0002c0008t0002g0068 others(1): Show |
4 | HG01261.hp1 HG02148.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-8221C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976985 | |||||||
| chr12:116977072 | T | C | 10 | a0002c0002t0002g0072 a0002c0002t0002g0077 a0002c0002t0002g0079 others(7): Show |
10 | HG02071.hp2 NA18954.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.836-8134T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977072 | |||||||
| chr12:116977169 | C | T | 6 | a0001c0001t0001g0159 a0001c0001t0001g0189 a0001c0001t0001g0225 others(3): Show |
6 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-8037C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977169 | |||||||
| chr12:116977280 | C | A | 2 | a0002c0002t0005g0064 a0002c0002t0005g0100 |
2 | HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.836-7926C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977280 | |||||||
| chr12:116977337 | G | A | 4 | a0001c0001t0003g0051 a0003c0003t0003g0166 a0003c0003t0003g0192 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-7869G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977337 | |||||||
| chr12:116977345 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.836-7861G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977345 | |||||||
| chr12:116977357 | A | G | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-7849A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977357 | |||||||
| chr12:116977488 | G | A | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.836-7718G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977488 | |||||||
| chr12:116977538 | G | A | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.836-7668G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977538 | |||||||
| chr12:116977763 | A | G | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.836-7443A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977763 | |||||||
| chr12:116977997 | C | T | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.836-7209C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977997 | |||||||
| chr12:116978064 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.836-7142A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978064 | |||||||
| chr12:116978080 | C | T | 2 | a0003c0003t0010g0013 a0003c0003t0010g0014 |
2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.836-7126C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978080 | |||||||
| chr12:116978188 | A | C | 8 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0089 others(5): Show |
9 | HG01175.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.836-7018A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978188 | |||||||
| chr12:116978349 | T | G | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.836-6857T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978349 | |||||||
| chr12:116978506 | T | A | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-6700T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978506 | |||||||
| chr12:116978536 | A | C | 1 | a0002c0002t0002g0080 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.836-6670A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978536 | |||||||
| chr12:116978541 | A | C | 1 | a0001c0001t0032g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.836-6665A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978541 | |||||||
| chr12:116978753 | G | A | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.836-6453G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978753 | |||||||
| chr12:116978864 | T | C | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.836-6342T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978864 | |||||||
| chr12:116979361 | G | A | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.836-5845G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116979361 | |||||||
| chr12:116979727 | T | C | 11 | a0003c0005t0002g0055 a0003c0005t0002g0056 a0003c0005t0002g0057 others(8): Show |
12 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.836-5479T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116979727 | |||||||
| chr12:116979777 | C | CA | 65 | a0001c0001t0001g0048 a0001c0001t0001g0159 a0001c0001t0001g0164 others(62): Show |
65 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.836-5410dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116979777 | ||||||
| chr12:116979777 | C | CAA | 24 | a0001c0001t0001g0177 a0001c0001t0003g0050 a0001c0001t0003g0051 others(21): Show |
24 | HG01891.hp2 HG02055.hp2 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.836-5411_836-5410d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116979777 | ||||||
| chr12:116979777 | CA | C | 18 | a0001c0001t0001g0239 a0003c0003t0006g0009 a0003c0003t0010g0013 others(15): Show |
19 | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.836-5410delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116979777 | ||||||
| chr12:116979814 | A | G | 1 | a0003c0005t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.836-5392A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116979814 | |||||||
| chr12:116980034 | G | C | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.836-5172G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116980034 | |||||||
| chr12:116980454 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.836-4752T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116980454 | |||||||
| chr12:116980664 | C | T | 1 | a0001c0001t0004g0036 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.836-4542C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116980664 | |||||||
| chr12:116981002 | C | T | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.836-4204C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981002 | |||||||
| chr12:116981060 | T | C | 5 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(2): Show |
6 | HG02723.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-4146T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981060 | |||||||
| chr12:116981349 | T | C | 13 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(10): Show |
14 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.836-3857T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981349 | |||||||
| chr12:116981589 | A | G | 15 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(12): Show |
16 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.836-3617A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981589 | |||||||
| chr12:116981613 | CT | C | 143 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(140): Show |
143 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.836-3579delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116981613 | ||||||
| chr12:116981770 | T | C | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.836-3436T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981770 | |||||||
| chr12:116982112 | A | T | 1 | a0002c0008t0002g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.836-3094A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982112 | |||||||
| chr12:116982290 | C | T | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-2916C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982290 | |||||||
| chr12:116982308 | T | A | 11 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(8): Show |
11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.836-2898T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982308 | |||||||
| chr12:116982333 | C | G | 157 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.836-2873C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982333 | |||||||
| chr12:116982374 | A | T | 17 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(14): Show |
18 | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.836-2832A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982374 | |||||||
| chr12:116982623 | A | AT | 99 | a0002c0002t0001g0146 a0002c0002t0002g0003 a0002c0002t0002g0030 others(96): Show |
103 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.836-2566dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116982623 | ||||||
| chr12:116982623 | A | ATT | 9 | a0002c0002t0002g0096 a0002c0002t0002g0141 a0002c0011t0002g0130 others(6): Show |
10 | HG01192.hp2 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.836-2567_836-2566d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116982623 | ||||||
| chr12:116982623 | AT | A | 156 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(153): Show |
156 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.836-2566delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116982623 | ||||||
| chr12:116982900 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.836-2306C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982900 | |||||||
| chr12:116982957 | G | A | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.836-2249G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982957 | |||||||
| chr12:116982975 | A | C | 178 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(175): Show |
180 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.836-2231A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982975 | |||||||
| chr12:116983142 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.836-2064T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983142 | |||||||
| chr12:116983284 | A | G | 4 | a0001c0001t0001g0223 a0001c0001t0001g0251 a0001c0001t0015g0220 others(1): Show |
4 | HG01258.hp2 HG02293.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-1922A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983284 | |||||||
| chr12:116983336 | G | C | 1 | a0002c0002t0008g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.836-1870G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983336 | |||||||
| chr12:116983366 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.836-1840C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983366 | |||||||
| chr12:116983375 | C | T | 30 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(27): Show |
30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.836-1831C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983375 | |||||||
| chr12:116983408 | T | C | 1 | a0002c0002t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.836-1798T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983408 | |||||||
| chr12:116983527 | C | T | 11 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(8): Show |
11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.836-1679C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983527 | |||||||
| chr12:116983847 | G | A | 18 | a0001c0001t0001g0233 a0001c0001t0004g0031 a0001c0001t0004g0032 others(15): Show |
18 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.836-1359G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983847 | |||||||
| chr12:116983933 | A | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.836-1273A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983933 | |||||||
| chr12:116983937 | A | G | 98 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(95): Show |
98 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.836-1269A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983937 | |||||||
| chr12:116984050 | A | G | 1 | a0002c0002t0002g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.836-1156A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984050 | |||||||
| chr12:116984117 | G | A | 157 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.836-1089G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984117 | |||||||
| chr12:116984187 | T | G | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.836-1019T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984187 | |||||||
| chr12:116984310 | C | T | 152 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.836-896C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984310 | |||||||
| chr12:116984561 | C | T | 1 | a0002c0002t0005g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.836-645C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984561 | |||||||
| chr12:116984587 | G | T | 152 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.836-619G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984587 | |||||||
| chr12:116984844 | G | C | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.836-362G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984844 | |||||||
| chr12:116984845 | C | T | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.836-361C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984845 | |||||||
| chr12:116984863 | G | A | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.836-343G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984863 | |||||||
| chr12:116984867 | G | A | 6 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.836-339G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984867 | |||||||
| chr12:116984922 | C | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-284C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984922 | |||||||
| chr12:116984983 | T | C | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-223T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984983 | |||||||
| chr12:116985063 | G | A | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.836-143G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116985063 | |||||||
| chr12:116985140 | T | A | 2 | a0003c0003t0010g0013 a0003c0003t0010g0014 |
2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.836-66T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116985140 | |||||||
| chr12:116985459 | G | A | 170 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1032+57G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985459 | |||||||
| chr12:116985466 | C | T | 4 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(1): Show |
4 | HG01433.hp2 HG02040.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+64C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985466 | |||||||
| chr12:116985617 | G | A | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+215G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985617 | |||||||
| chr12:116985663 | G | A | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+261G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985663 | |||||||
| chr12:116985984 | T | A | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+582T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985984 | |||||||
| chr12:116986357 | C | A | 1 | a0004c0004t0001g0185 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1032+955C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986357 | |||||||
| chr12:116986500 | C | T | 1 | a0002c0002t0005g0107 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1032+1098C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986500 | |||||||
| chr12:116986577 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0282 |
3 | HG02818.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1032+1175G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986577 | |||||||
| chr12:116986596 | A | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1032+1194A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986596 | |||||||
| chr12:116986625 | C | CA | 30 | a0001c0001t0001g0233 a0001c0001t0004g0031 a0001c0001t0004g0037 others(27): Show |
32 | HG00609.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1032+1236dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116986625 | ||||||
| chr12:116986631 | AAAAAAAA others(3): Show |
A | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1032+1237_1032+124 others(14): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116986631 | ||||||
| chr12:116986649 | C | A | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1032+1247C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986649 | |||||||
| chr12:116986650 | A | G | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1032+1248A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986650 | |||||||
| chr12:116986661 | G | A | 1 | a0002c0008t0002g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1032+1259G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986661 | |||||||
| chr12:116986701 | T | A | 141 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(138): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.1032+1299T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986701 | |||||||
| chr12:116987169 | C | T | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1033-1494C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987169 | |||||||
| chr12:116987189 | A | T | 1 | a0002c0002t0030g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1033-1474A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987189 | |||||||
| chr12:116987207 | T | A | 2 | a0002c0002t0002g0090 a0002c0002t0024g0065 |
2 | HG01175.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1033-1456T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987207 | |||||||
| chr12:116987212 | G | A | 1 | a0001c0001t0004g0041 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1033-1451G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987212 | |||||||
| chr12:116987235 | G | A | 157 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1033-1428G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987235 | |||||||
| chr12:116987267 | A | G | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1033-1396A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987267 | |||||||
| chr12:116987349 | T | G | 11 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(8): Show |
11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1033-1314T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987349 | |||||||
| chr12:116987376 | G | T | 1 | a0004c0004t0001g0260 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1033-1287G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987376 | |||||||
| chr12:116987451 | C | G | 104 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(101): Show |
104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1033-1212C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987451 | |||||||
| chr12:116987631 | A | G | 188 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(185): Show |
190 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1033-1032A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987631 | |||||||
| chr12:116987645 | A | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033-1018A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987645 | |||||||
| chr12:116987692 | TAAAC | T | 6 | a0002c0002t0002g0104 a0002c0002t0002g0105 a0005c0007t0007g0002 others(3): Show |
7 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-955_1033-952d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116987692 | ||||||
| chr12:116987708 | CAAAA | C | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033-952_1033-949d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116987708 | ||||||
| chr12:116987726 | C | CA | 6 | a0001c0001t0003g0191 a0001c0001t0003g0198 a0001c0001t0003g0199 others(3): Show |
6 | HG00423.hp1 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1033-930dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116987726 | ||||||
| chr12:116987733 | A | C | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1033-930A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987733 | |||||||
| chr12:116987761 | A | G | 1 | a0003c0003t0010g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1033-902A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987761 | |||||||
| chr12:116987864 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1033-799G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987864 | |||||||
| chr12:116987890 | C | T | 8 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0003t0012g0020 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-773C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987890 | |||||||
| chr12:116987948 | A | G | 1 | a0001c0001t0001g0274 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1033-715A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987948 | |||||||
| chr12:116988311 | C | T | 18 | a0001c0001t0001g0233 a0001c0001t0004g0031 a0001c0001t0004g0032 others(15): Show |
18 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.1033-352C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116988311 | |||||||
| chr12:116988312 | C | G | 2 | a0004c0004t0001g0254 a0004c0004t0001g0258 |
2 | NA18994.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1033-351C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116988312 | |||||||
| chr12:116988601 | T | C | 1 | a0001c0001t0004g0041 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1033-62T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116988601 | |||||||
| chr12:116989409 | A | G | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1239+540A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116989409 | |||||||
| chr12:116989550 | A | G | 9 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(6): Show |
9 | HG02040.hp2 NA18954.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+681A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116989550 | |||||||
| chr12:116989843 | A | G | 3 | a0001c0001t0003g0202 a0001c0001t0003g0203 a0001c0001t0003g0214 |
3 | HG01168.hp2 HG01169.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1239+974A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116989843 | |||||||
| chr12:116989898 | G | A | 1 | a0002c0002t0002g0080 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1239+1029G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116989898 | |||||||
| chr12:116990052 | T | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1239+1183T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990052 | |||||||
| chr12:116990180 | C | T | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+1311C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990180 | |||||||
| chr12:116990321 | G | A | 2 | a0004c0004t0001g0256 a0004c0004t0001g0267 |
2 | HG00438.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1239+1452G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990321 | |||||||
| chr12:116990481 | G | C | 4 | a0001c0001t0003g0051 a0003c0003t0003g0166 a0003c0003t0003g0192 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+1612G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990481 | |||||||
| chr12:116990613 | CT | C | 44 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(41): Show |
44 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1239+1749delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116990613 | ||||||
| chr12:116990666 | A | G | 1 | a0003c0003t0029g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1239+1797A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990666 | |||||||
| chr12:116990792 | A | G | 8 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(5): Show |
9 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+1923A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990792 | |||||||
| chr12:116990997 | C | A | 2 | a0001c0001t0003g0205 a0001c0001t0003g0212 |
2 | NA18747.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1239+2128C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990997 | |||||||
| chr12:116991035 | G | A | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+2166G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991035 | |||||||
| chr12:116991161 | CAT | C | 7 | a0001c0001t0001g0164 a0001c0001t0001g0215 a0001c0001t0001g0262 others(4): Show |
7 | HG01192.hp1 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+2293_1239+229 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991161 | |||||||
| chr12:116991273 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1239+2404A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991273 | |||||||
| chr12:116991490 | G | A | 1 | a0004c0004t0001g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1239+2621G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991490 | |||||||
| chr12:116991936 | T | A | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+3067T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991936 | |||||||
| chr12:116991994 | A | T | 1 | a0001c0001t0003g0156 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1239+3125A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991994 | |||||||
| chr12:116992163 | C | T | 3 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0035 |
3 | HG03491.hp2 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1239+3294C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992163 | |||||||
| chr12:116992262 | A | T | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1239+3393A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992262 | |||||||
| chr12:116992399 | CT | C | 35 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(32): Show |
37 | HG00741.hp1 HG01106.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1239+3540delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992399 | ||||||
| chr12:116992418 | G | C | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+3549G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992418 | |||||||
| chr12:116992420 | G | GT | 25 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(22): Show |
27 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1239+3555dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992420 | ||||||
| chr12:116992425 | G | GT | 25 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(22): Show |
25 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1239+3566dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992425 | ||||||
| chr12:116992425 | G | GTT | 12 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(9): Show |
12 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1239+3565_1239+356 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992425 | ||||||
| chr12:116992425 | G | T | 35 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(32): Show |
37 | HG00741.hp1 HG01106.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1239+3556G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992425 | |||||||
| chr12:116992441 | G | A | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.1239+3572G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992441 | |||||||
| chr12:116992595 | C | G | 1 | a0007c0012t0018g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1239+3726C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992595 | |||||||
| chr12:116992761 | G | GGT | 29 | a0001c0001t0001g0157 a0001c0001t0001g0227 a0001c0001t0001g0228 others(26): Show |
30 | HG00323.hp2 HG01175.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1239+3927_1239+392 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | ||||||
| chr12:116992761 | G | GGTGT | 44 | a0001c0001t0001g0171 a0001c0001t0001g0177 a0001c0001t0001g0181 others(41): Show |
44 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1239+3925_1239+392 others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | ||||||
| chr12:116992761 | G | GGTGTGT | 91 | a0001c0001t0001g0048 a0001c0001t0001g0159 a0001c0001t0001g0164 others(88): Show |
94 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1239+3923_1239+392 others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | ||||||
| chr12:116992761 | G | GGTGTGTG others(1): Show |
29 | a0001c0001t0001g0174 a0001c0001t0001g0184 a0001c0001t0001g0188 others(26): Show |
29 | HG00642.hp1 HG01106.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1239+3921_1239+392 others(12): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | ||||||
| chr12:116992761 | G | GGTGTGTG others(3): Show |
16 | a0001c0001t0001g0180 a0001c0001t0001g0223 a0001c0001t0001g0236 others(13): Show |
16 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.1239+3919_1239+392 others(14): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | ||||||
| chr12:116992761 | G | GGTGTGTG others(5): Show |
3 | a0001c0001t0001g0272 a0001c0001t0003g0163 a0002c0008t0002g0067 |
3 | HG02148.hp1 HG02293.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1239+3917_1239+392 others(16): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | ||||||
| chr12:116992761 | GGT | G | 41 | a0002c0002t0002g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(38): Show |
41 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1239+3927_1239+392 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | ||||||
| chr12:116992761 | GGTGTGTG others(9): Show |
G | 3 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 |
3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1239+3913_1239+392 others(20): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | ||||||
| chr12:116992867 | T | A | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+3998T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992867 | |||||||
| chr12:116993044 | A | G | 138 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1239+4175A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993044 | |||||||
| chr12:116993098 | C | CT | 153 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0164 others(150): Show |
154 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1239+4252dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116993098 | ||||||
| chr12:116993098 | C | CTT | 25 | a0001c0001t0001g0159 a0001c0001t0001g0169 a0001c0001t0001g0173 others(22): Show |
25 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1239+4251_1239+425 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116993098 | ||||||
| chr12:116993129 | C | T | 4 | a0001c0001t0001g0215 a0001c0001t0001g0262 a0001c0001t0001g0266 others(1): Show |
4 | HG01192.hp1 HG01433.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+4260C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993129 | |||||||
| chr12:116993208 | G | A | 25 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(22): Show |
26 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1239+4339G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993208 | |||||||
| chr12:116993276 | G | A | 2 | a0002c0002t0002g0127 a0002c0002t0027g0140 |
2 | HG01975.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1239+4407G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993276 | |||||||
| chr12:116993392 | G | A | 5 | a0003c0005t0002g0055 a0003c0005t0002g0056 a0003c0005t0002g0057 others(2): Show |
5 | HG02257.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+4523G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993392 | |||||||
| chr12:116993398 | G | A | 25 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(22): Show |
26 | HG01175.hp1 HG01192.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1239+4529G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993398 | |||||||
| chr12:116993657 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1239+4788A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993657 | |||||||
| chr12:116993664 | G | C | 1 | a0004c0004t0001g0185 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1239+4795G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993664 | |||||||
| chr12:116993799 | C | T | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+4930C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993799 | |||||||
| chr12:116993898 | T | G | 39 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(36): Show |
39 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1239+5029T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993898 | |||||||
| chr12:116993955 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1239+5086A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993955 | |||||||
| chr12:116994199 | A | G | 234 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(231): Show |
236 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1239+5330A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994199 | |||||||
| chr12:116994220 | GGTACTGG others(7): Show |
G | 1 | a0001c0001t0003g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1239+5369_1239+538 others(18): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116994220 | ||||||
| chr12:116994312 | A | C | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+5443A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994312 | |||||||
| chr12:116994429 | G | A | 263 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(260): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.1239+5560G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994429 | |||||||
| chr12:116994457 | G | C | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+5588G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994457 | |||||||
| chr12:116994562 | T | C | 1 | a0003c0003t0006g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1239+5693T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994562 | |||||||
| chr12:116994707 | T | C | 2 | a0003c0003t0010g0016 a0008c0018t0002g0015 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1239+5838T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994707 | |||||||
| chr12:116994802 | T | G | 1 | a0002c0002t0002g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1239+5933T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994802 | |||||||
| chr12:116994822 | T | TTG | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1239+5955_1239+595 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116994822 | ||||||
| chr12:116994873 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1239+6004A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994873 | |||||||
| chr12:116994922 | A | G | 1 | a0002c0002t0002g0135 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1239+6053A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994922 | |||||||
| chr12:116995003 | T | G | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1239+6134T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116995003 | |||||||
| chr12:116995292 | C | T | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1239+6423C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116995292 | |||||||
| chr12:116995471 | T | G | 1 | a0005c0007t0002g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1239+6602T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116995471 | |||||||
| chr12:116995854 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0279 others(1): Show |
4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+6985G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116995854 | |||||||
| chr12:116996004 | G | A | 23 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0076 others(20): Show |
23 | HG00408.hp2 HG00621.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1239+7135G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996004 | |||||||
| chr12:116996008 | G | A | 1 | a0002c0002t0002g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1239+7139G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996008 | |||||||
| chr12:116996106 | A | G | 1 | a0004c0004t0001g0185 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1239+7237A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996106 | |||||||
| chr12:116996308 | G | A | 2 | a0003c0003t0006g0006 a0003c0003t0006g0008 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1239+7439G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996308 | |||||||
| chr12:116996340 | C | T | 30 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(27): Show |
30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1239+7471C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996340 | |||||||
| chr12:116996407 | A | T | 188 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(185): Show |
190 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1239+7538A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996407 | |||||||
| chr12:116996497 | T | A | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+7628T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996497 | |||||||
| chr12:116996501 | AGT | A | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+7633_1239+763 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996501 | |||||||
| chr12:116996512 | C | CA | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1239+7653dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116996512 | ||||||
| chr12:116996527 | G | A | 1 | a0001c0001t0004g0037 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1239+7658G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996527 | |||||||
| chr12:116996589 | A | T | 1 | a0003c0003t0006g0009 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1239+7720A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996589 | |||||||
| chr12:116996784 | G | A | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1239+7915G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996784 | |||||||
| chr12:116996906 | C | T | 1 | a0001c0001t0004g0038 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1239+8037C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996906 | |||||||
| chr12:116997211 | T | C | 240 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(237): Show |
242 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1239+8342T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997211 | |||||||
| chr12:116997268 | A | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1239+8399A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997268 | |||||||
| chr12:116997303 | C | G | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1239+8434C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997303 | |||||||
| chr12:116997307 | G | A | 1 | a0002c0002t0030g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1239+8438G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997307 | |||||||
| chr12:116997504 | G | A | 1 | a0002c0002t0005g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1239+8635G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997504 | |||||||
| chr12:116997566 | C | T | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1239+8697C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997566 | |||||||
| chr12:116997670 | C | T | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1239+8801C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997670 | |||||||
| chr12:116997877 | G | A | 5 | a0003c0005t0002g0055 a0003c0005t0002g0056 a0003c0005t0002g0057 others(2): Show |
5 | HG02257.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+9008G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997877 | |||||||
| chr12:116997959 | G | T | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+9090G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997959 | |||||||
| chr12:116997961 | G | A | 1 | a0003c0005t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1239+9092G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997961 | |||||||
| chr12:116997964 | T | C | 27 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(24): Show |
29 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1239+9095T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997964 | |||||||
| chr12:116998074 | C | G | 5 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(2): Show |
5 | HG02132.hp2 NA18964.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239+9205C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998074 | |||||||
| chr12:116998164 | G | C | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1239+9295G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998164 | |||||||
| chr12:116998194 | G | C | 180 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(177): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1239+9325G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998194 | |||||||
| chr12:116998380 | C | CT | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1239+9512dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116998380 | ||||||
| chr12:116998581 | C | G | 1 | a0002c0002t0002g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1239+9712C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998581 | |||||||
| chr12:116998721 | TC | T | 138 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1239+9854delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116998721 | ||||||
| chr12:116998780 | A | G | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+9911A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998780 | |||||||
| chr12:116998880 | C | G | 1 | a0002c0002t0002g0129 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1239+10011C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998880 | |||||||
| chr12:116998906 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1239+10037C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998906 | |||||||
| chr12:116999056 | C | T | 271 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(268): Show |
276 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1239+10187C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999056 | |||||||
| chr12:116999067 | A | G | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1239+10198A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999067 | |||||||
| chr12:116999085 | C | T | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+10216C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999085 | |||||||
| chr12:116999204 | C | G | 1 | a0001c0001t0001g0285 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1239+10335C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999204 | |||||||
| chr12:116999361 | A | G | 8 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0003t0012g0020 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1239+10492A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999361 | |||||||
| chr12:116999531 | C | T | 1 | a0002c0002t0005g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1239+10662C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999531 | |||||||
| chr12:116999566 | C | T | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+10697C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999566 | |||||||
| chr12:116999583 | G | A | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+10714G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999583 | |||||||
| chr12:116999613 | C | T | 2 | a0001c0009t0001g0187 a0001c0009t0001g0246 |
2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1240-10710C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999613 | |||||||
| chr12:116999624 | CT | C | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-10697delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116999624 | ||||||
| chr12:116999646 | G | A | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1240-10677G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999646 | |||||||
| chr12:116999672 | G | C | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1240-10651G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999672 | |||||||
| chr12:116999981 | A | AT | 156 | a0001c0001t0001g0048 a0001c0001t0001g0159 a0001c0001t0001g0164 others(153): Show |
157 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1240-10322dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116999981 | ||||||
| chr12:116999981 | A | ATT | 8 | a0001c0001t0001g0184 a0001c0001t0001g0233 a0001c0001t0031g0049 others(5): Show |
8 | HG00438.hp1 HG01261.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240-10323_1240-10 others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116999981 | ||||||
| chr12:117000008 | G | A | 1 | a0001c0001t0003g0201 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1240-10315G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000008 | |||||||
| chr12:117000015 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1240-10308G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000015 | |||||||
| chr12:117000045 | G | A | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-10278G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000045 | |||||||
| chr12:117000054 | T | C | 16 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(13): Show |
17 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1240-10269T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000054 | |||||||
| chr12:117000255 | C | T | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-10068C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000255 | |||||||
| chr12:117000327 | T | C | 8 | a0001c0001t0004g0032 a0001c0001t0004g0037 a0001c0001t0004g0038 others(5): Show |
8 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240-9996T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000327 | |||||||
| chr12:117000358 | C | T | 99 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1240-9965C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000358 | |||||||
| chr12:117000501 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1240-9822C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000501 | |||||||
| chr12:117000518 | C | T | 2 | a0001c0001t0003g0191 a0001c0001t0003g0230 |
2 | NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1240-9805C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000518 | |||||||
| chr12:117000519 | G | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0244 others(1): Show |
4 | HG02258.hp1 HG03491.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-9804G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000519 | |||||||
| chr12:117000531 | C | G | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-9792C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000531 | |||||||
| chr12:117000717 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1240-9606G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000717 | |||||||
| chr12:117000833 | A | G | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-9490A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000833 | |||||||
| chr12:117000893 | A | G | 1 | a0001c0001t0003g0190 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1240-9430A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000893 | |||||||
| chr12:117001134 | T | C | 159 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1240-9189T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001134 | |||||||
| chr12:117001342 | GCTGCCTG others(1): Show |
G | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240-8975_1240-896 others(12): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117001342 | ||||||
| chr12:117001360 | T | G | 1 | a0001c0001t0004g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1240-8963T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001360 | |||||||
| chr12:117001376 | C | G | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240-8947C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001376 | |||||||
| chr12:117001410 | G | C | 2 | a0001c0001t0003g0148 a0009c0016t0003g0029 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1240-8913G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001410 | |||||||
| chr12:117001611 | A | T | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-8712A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001611 | |||||||
| chr12:117001649 | G | A | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-8674G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001649 | |||||||
| chr12:117001767 | G | A | 1 | a0002c0008t0002g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1240-8556G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001767 | |||||||
| chr12:117001903 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1240-8420C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001903 | |||||||
| chr12:117001974 | G | A | 2 | a0002c0002t0002g0076 a0002c0002t0002g0113 |
2 | NA18953.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1240-8349G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001974 | |||||||
| chr12:117002315 | C | T | 3 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 |
3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1240-8008C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002315 | |||||||
| chr12:117002415 | G | A | 45 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(42): Show |
46 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.1240-7908G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002415 | |||||||
| chr12:117002468 | T | G | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1240-7855T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002468 | |||||||
| chr12:117002598 | C | G | 6 | a0002c0002t0011g0082 a0002c0002t0011g0147 a0003c0003t0011g0010 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240-7725C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002598 | |||||||
| chr12:117002603 | G | A | 30 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(27): Show |
30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1240-7720G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002603 | |||||||
| chr12:117002631 | T | G | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-7692T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002631 | |||||||
| chr12:117002742 | A | T | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-7581A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002742 | |||||||
| chr12:117002828 | T | C | 281 | a0001c0001t0001g0048 a0001c0001t0001g0157 a0001c0001t0001g0159 others(278): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1240-7495T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002828 | |||||||
| chr12:117002877 | C | T | 1 | a0002c0008t0002g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1240-7446C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002877 | |||||||
| chr12:117002898 | G | A | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-7425G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002898 | |||||||
| chr12:117003153 | T | C | 4 | a0002c0008t0002g0066 a0002c0008t0002g0067 a0002c0008t0002g0068 others(1): Show |
4 | HG01261.hp1 HG02148.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-7170T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003153 | |||||||
| chr12:117003218 | C | T | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1240-7105C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003218 | |||||||
| chr12:117003364 | C | T | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.1240-6959C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003364 | |||||||
| chr12:117003367 | A | T | 45 | a0002c0002t0001g0146 a0002c0002t0002g0072 a0002c0002t0002g0073 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1240-6956A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003367 | |||||||
| chr12:117003484 | A | ATTG | 126 | a0002c0002t0001g0146 a0002c0002t0002g0003 a0002c0002t0002g0030 others(123): Show |
131 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1240-6836_1240-683 others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117003484 | ||||||
| chr12:117003538 | T | C | 7 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0238 others(4): Show |
7 | HG01109.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240-6785T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003538 | |||||||
| chr12:117003668 | C | G | 1 | a0002c0002t0005g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1240-6655C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003668 | |||||||
| chr12:117004012 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1240-6311T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004012 | |||||||
| chr12:117004189 | T | C | 3 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 |
3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1240-6134T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004189 | |||||||
| chr12:117004367 | T | C | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-5956T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004367 | |||||||
| chr12:117004402 | T | C | 1 | a0002c0002t0002g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1240-5921T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004402 | |||||||
| chr12:117004499 | G | A | 45 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(42): Show |
46 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.1240-5824G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004499 | |||||||
| chr12:117004767 | GTCTCCTG others(10): Show |
G | 184 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(181): Show |
189 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1240-5533_1240-551 others(21): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117004767 | ||||||
| chr12:117004774 | G | A | 24 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0176 others(21): Show |
24 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1240-5549G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004774 | |||||||
| chr12:117004831 | T | C | 184 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(181): Show |
189 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1240-5492T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004831 | |||||||
| chr12:117004900 | A | G | 1 | a0002c0002t0008g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1240-5423A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004900 | |||||||
| chr12:117005016 | G | T | 2 | a0002c0002t0009g0060 a0002c0002t0009g0062 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1240-5307G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005016 | |||||||
| chr12:117005097 | A | G | 49 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(46): Show |
52 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.1240-5226A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005097 | |||||||
| chr12:117005203 | G | A | 2 | a0001c0001t0003g0207 a0001c0001t0003g0211 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1240-5120G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005203 | |||||||
| chr12:117005277 | C | T | 6 | a0005c0007t0002g0026 a0005c0007t0007g0002 a0005c0007t0007g0023 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240-5046C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005277 | |||||||
| chr12:117005329 | C | T | 4 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(1): Show |
4 | HG00423.hp1 HG02083.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-4994C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005329 | |||||||
| chr12:117005754 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1240-4569C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005754 | |||||||
| chr12:117005786 | C | T | 143 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(140): Show |
148 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1240-4537C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005786 | |||||||
| chr12:117005945 | C | T | 1 | a0002c0002t0008g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1240-4378C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005945 | |||||||
| chr12:117005965 | C | G | 6 | a0001c0001t0001g0159 a0001c0001t0001g0189 a0001c0001t0001g0225 others(3): Show |
6 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240-4358C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005965 | |||||||
| chr12:117006039 | T | C | 2 | a0002c0002t0005g0064 a0002c0002t0005g0100 |
2 | HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1240-4284T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006039 | |||||||
| chr12:117006232 | T | C | 3 | a0002c0002t0002g0003 a0002c0002t0002g0089 a0002c0002t0002g0091 |
4 | HG02109.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-4091T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006232 | |||||||
| chr12:117006295 | A | G | 2 | a0001c0001t0003g0148 a0009c0016t0003g0029 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1240-4028A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006295 | |||||||
| chr12:117006385 | T | C | 1 | a0003c0003t0010g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1240-3938T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006385 | |||||||
| chr12:117006442 | C | T | 4 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-3881C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006442 | |||||||
| chr12:117006519 | C | T | 1 | a0003c0003t0021g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1240-3804C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006519 | |||||||
| chr12:117006544 | G | A | 1 | a0002c0002t0008g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1240-3779G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006544 | |||||||
| chr12:117006662 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | NA18969.hp1 NA18975.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1240-3661G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006662 | |||||||
| chr12:117006731 | A | G | 11 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(8): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1240-3592A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006731 | |||||||
| chr12:117006980 | T | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-3343T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006980 | |||||||
| chr12:117007154 | C | G | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240-3169C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007154 | |||||||
| chr12:117007174 | T | C | 2 | a0002c0002t0009g0060 a0002c0002t0009g0062 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1240-3149T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007174 | |||||||
| chr12:117007240 | G | T | 14 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(11): Show |
15 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240-3083G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007240 | |||||||
| chr12:117007252 | G | T | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.1240-3071G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007252 | |||||||
| chr12:117007261 | GA | G | 21 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(18): Show |
22 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1240-3051delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117007261 | ||||||
| chr12:117007377 | C | A | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-2946C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007377 | |||||||
| chr12:117007525 | A | G | 1 | a0002c0002t0002g0139 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1240-2798A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007525 | |||||||
| chr12:117007725 | A | G | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-2598A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007725 | |||||||
| chr12:117007753 | A | G | 1 | a0003c0005t0002g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1240-2570A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007753 | |||||||
| chr12:117007784 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1240-2539A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007784 | |||||||
| chr12:117007832 | G | A | 43 | a0002c0002t0002g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(40): Show |
43 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1240-2491G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007832 | |||||||
| chr12:117007867 | C | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-2456C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007867 | |||||||
| chr12:117007874 | C | A | 2 | a0003c0003t0010g0013 a0003c0003t0010g0014 |
2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1240-2449C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007874 | |||||||
| chr12:117008173 | C | T | 1 | a0001c0006t0001g0270 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1240-2150C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117008173 | |||||||
| chr12:117008758 | CAT | C | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-1564_1240-156 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117008758 | |||||||
| chr12:117008829 | G | T | 1 | a0003c0005t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1240-1494G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117008829 | |||||||
| chr12:117008959 | C | G | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1240-1364C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117008959 | |||||||
| chr12:117009021 | C | T | 1 | a0002c0002t0002g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1240-1302C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009021 | |||||||
| chr12:117009207 | A | C | 4 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-1116A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009207 | |||||||
| chr12:117009286 | G | A | 1 | a0001c0001t0032g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1240-1037G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009286 | |||||||
| chr12:117009395 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-928A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009395 | |||||||
| chr12:117009502 | G | C | 2 | a0001c0001t0003g0148 a0009c0016t0003g0029 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1240-821G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009502 | |||||||
| chr12:117009606 | GTTGAA | G | 6 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(3): Show |
6 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-709_1240-705d others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117009606 | ||||||
| chr12:117009695 | T | C | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-628T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009695 | |||||||
| chr12:117009739 | A | G | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-584A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009739 | |||||||
| chr12:117009852 | A | C | 1 | a0003c0003t0006g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1240-471A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009852 | |||||||
| chr12:117010092 | A | G | 10 | a0002c0002t0011g0082 a0002c0002t0011g0147 a0003c0003t0011g0010 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240-231A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117010092 | |||||||
| chr12:117010667 | G | C | 2 | a0004c0004t0001g0254 a0004c0004t0001g0258 |
2 | NA18994.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1367+217G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010667 | |||||||
| chr12:117010698 | G | A | 24 | a0002c0002t0002g0072 a0002c0002t0002g0074 a0002c0002t0002g0076 others(21): Show |
24 | HG00408.hp2 HG00621.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1367+248G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010698 | |||||||
| chr12:117010756 | ATTTG | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0244 others(1): Show |
4 | HG02258.hp1 HG03491.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+311_1367+314d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117010756 | ||||||
| chr12:117010843 | C | T | 1 | a0002c0002t0002g0131 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1367+393C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010843 | |||||||
| chr12:117010983 | C | T | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+533C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010983 | |||||||
| chr12:117010993 | C | T | 10 | a0002c0002t0005g0064 a0002c0002t0005g0092 a0002c0002t0005g0094 others(7): Show |
10 | HG00323.hp1 HG00642.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367+543C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010993 | |||||||
| chr12:117011017 | C | T | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1367+567C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011017 | |||||||
| chr12:117011031 | A | T | 6 | a0002c0002t0011g0082 a0002c0002t0011g0147 a0003c0003t0011g0010 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+581A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011031 | |||||||
| chr12:117011127 | C | CTTTTT | 43 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(40): Show |
44 | HG00544.hp1 HG00741.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1367+688_1367+692d others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117011127 | ||||||
| chr12:117011127 | C | CTTTTTT | 35 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0163 others(32): Show |
35 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1367+687_1367+692d others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117011127 | ||||||
| chr12:117011127 | C | CTTTTTTT | 53 | a0001c0001t0003g0204 a0002c0002t0002g0003 a0002c0002t0002g0030 others(50): Show |
57 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.1367+686_1367+692d others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117011127 | ||||||
| chr12:117011127 | C | CTTTTTTT others(1): Show |
42 | a0002c0002t0002g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(39): Show |
42 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1367+685_1367+692d others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117011127 | ||||||
| chr12:117011148 | G | A | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1367+698G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011148 | |||||||
| chr12:117011240 | G | A | 1 | a0002c0002t0002g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1367+790G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011240 | |||||||
| chr12:117011280 | C | T | 5 | a0002c0002t0002g0003 a0002c0002t0002g0089 a0002c0002t0002g0090 others(2): Show |
6 | HG01175.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+830C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011280 | |||||||
| chr12:117011358 | G | A | 3 | a0002c0002t0002g0093 a0002c0002t0002g0096 a0002c0002t0002g0133 |
3 | HG01192.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1367+908G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011358 | |||||||
| chr12:117011375 | C | A | 182 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(179): Show |
187 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.1367+925C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011375 | |||||||
| chr12:117011406 | C | G | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.1367+956C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011406 | |||||||
| chr12:117011449 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1367+999A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011449 | |||||||
| chr12:117011472 | G | A | 3 | a0001c0009t0001g0187 a0001c0009t0001g0246 a0001c0009t0001g0250 |
3 | HG02698.hp1 HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1367+1022G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011472 | |||||||
| chr12:117011514 | G | C | 1 | a0002c0002t0005g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1367+1064G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011514 | |||||||
| chr12:117011555 | C | T | 2 | a0001c0001t0003g0148 a0009c0016t0003g0029 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1367+1105C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011555 | |||||||
| chr12:117011594 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+1144A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011594 | |||||||
| chr12:117011659 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1367+1209T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011659 | |||||||
| chr12:117011664 | T | C | 1 | a0001c0001t0004g0031 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1367+1214T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011664 | |||||||
| chr12:117011876 | T | C | 1 | a0012c0014t0023g0078 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1367+1426T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011876 | |||||||
| chr12:117011925 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1367+1475C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011925 | |||||||
| chr12:117011947 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1367+1497G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011947 | |||||||
| chr12:117012190 | C | CTCATT | 87 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(84): Show |
90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1740_1367+174 others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012190 | |||||||
| chr12:117012192 | G | T | 87 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(84): Show |
90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1742G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012192 | |||||||
| chr12:117012194 | G | T | 87 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(84): Show |
90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1744G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012194 | |||||||
| chr12:117012196 | G | C | 87 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(84): Show |
90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1746G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012196 | |||||||
| chr12:117012197 | G | GCACTA | 87 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(84): Show |
90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1747_1367+174 others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012197 | |||||||
| chr12:117012236 | T | A | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+1786T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012236 | |||||||
| chr12:117012298 | T | A | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+1848T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012298 | |||||||
| chr12:117012375 | T | C | 1 | a0001c0001t0003g0200 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1367+1925T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012375 | |||||||
| chr12:117012683 | A | T | 114 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(111): Show |
119 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1367+2233A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012683 | |||||||
| chr12:117012803 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+2353A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012803 | |||||||
| chr12:117012959 | G | T | 2 | a0003c0003t0010g0016 a0008c0018t0002g0015 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1367+2509G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012959 | |||||||
| chr12:117013025 | G | A | 1 | a0002c0002t0002g0123 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1367+2575G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013025 | |||||||
| chr12:117013110 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+2660A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013110 | |||||||
| chr12:117013137 | G | T | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+2687G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013137 | |||||||
| chr12:117013235 | CCAT | C | 141 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(138): Show |
146 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1367+2790_1367+279 others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117013235 | ||||||
| chr12:117013343 | C | T | 1 | a0001c0006t0001g0183 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1367+2893C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013343 | |||||||
| chr12:117013375 | G | A | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+2925G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013375 | |||||||
| chr12:117013411 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1367+2961A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013411 | |||||||
| chr12:117013440 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1367+2990A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013440 | |||||||
| chr12:117013508 | G | A | 1 | a0011c0015t0003g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1367+3058G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013508 | |||||||
| chr12:117013610 | T | A | 2 | a0003c0003t0010g0013 a0003c0003t0010g0014 |
2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1367+3160T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013610 | |||||||
| chr12:117013624 | A | T | 4 | a0001c0001t0003g0195 a0003c0003t0003g0166 a0003c0003t0003g0192 others(1): Show |
4 | HG02976.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+3174A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013624 | |||||||
| chr12:117013625 | T | A | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1367+3175T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013625 | |||||||
| chr12:117013736 | T | TTTTA | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+3306_1367+330 others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117013736 | ||||||
| chr12:117013790 | A | G | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+3340A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013790 | |||||||
| chr12:117014098 | C | T | 1 | a0002c0002t0002g0138 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1367+3648C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014098 | |||||||
| chr12:117014146 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0232 a0002c0002t0001g0146 |
3 | HG00621.hp1 HG02071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1367+3696G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014146 | |||||||
| chr12:117014263 | T | TA | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+3818dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117014263 | ||||||
| chr12:117014339 | T | C | 1 | a0003c0003t0006g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1367+3889T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014339 | |||||||
| chr12:117014344 | T | A | 4 | a0003c0003t0006g0004 a0003c0003t0006g0151 a0003c0003t0006g0152 others(1): Show |
5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+3894T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014344 | |||||||
| chr12:117014361 | G | A | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+3911G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014361 | |||||||
| chr12:117014471 | C | T | 16 | a0001c0001t0001g0274 a0003c0003t0006g0004 a0003c0003t0006g0006 others(13): Show |
17 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1367+4021C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014471 | |||||||
| chr12:117014472 | G | A | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+4022G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014472 | |||||||
| chr12:117014538 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1367+4088G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014538 | |||||||
| chr12:117014634 | C | T | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+4184C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014634 | |||||||
| chr12:117014644 | T | G | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1367+4194T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014644 | |||||||
| chr12:117014649 | A | C | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1367+4199A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014649 | |||||||
| chr12:117014655 | T | G | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1367+4205T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014655 | |||||||
| chr12:117014724 | G | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0225 a0001c0001t0001g0227 others(1): Show |
4 | HG00323.hp2 HG01074.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+4274G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014724 | |||||||
| chr12:117014735 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+4285A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014735 | |||||||
| chr12:117014778 | T | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4328T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014778 | |||||||
| chr12:117014780 | G | T | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4330G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014780 | |||||||
| chr12:117014782 | C | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4332C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014782 | |||||||
| chr12:117014782 | C | T | 9 | a0002c0002t0002g0003 a0002c0002t0002g0089 a0002c0002t0002g0090 others(6): Show |
10 | HG00642.hp2 HG01175.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367+4332C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014782 | |||||||
| chr12:117014792 | T | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4342T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014792 | |||||||
| chr12:117014794 | A | G | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4344A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014794 | |||||||
| chr12:117014814 | GGGATGAG others(44): Show |
G | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4365_1367+441 others(55): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014814 | |||||||
| chr12:117014892 | T | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4442T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014892 | |||||||
| chr12:117014898 | T | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4448T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014898 | |||||||
| chr12:117014901 | C | T | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4451C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014901 | |||||||
| chr12:117014907 | T | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4457T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014907 | |||||||
| chr12:117014919 | T | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4469T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014919 | |||||||
| chr12:117014922 | C | G | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4472C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014922 | |||||||
| chr12:117014927 | A | T | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4477A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014927 | |||||||
| chr12:117014928 | C | G | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4478C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014928 | |||||||
| chr12:117014930 | G | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4480G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014930 | |||||||
| chr12:117014936 | T | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4486T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014936 | |||||||
| chr12:117014937 | G | T | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4487G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014937 | |||||||
| chr12:117014938 | G | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4488G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014938 | |||||||
| chr12:117014942 | G | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4492G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014942 | |||||||
| chr12:117014944 | A | ATCTCACT others(3): Show |
1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4494_1367+449 others(14): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014944 | |||||||
| chr12:117014947 | A | T | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4497A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014947 | |||||||
| chr12:117014948 | T | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4498T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014948 | |||||||
| chr12:117014949 | G | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4499G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014949 | |||||||
| chr12:117014953 | T | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4503T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014953 | |||||||
| chr12:117014955 | T | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4505T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014955 | |||||||
| chr12:117014959 | T | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4509T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014959 | |||||||
| chr12:117014960 | C | T | 3 | a0003c0003t0010g0017 a0003c0003t0010g0019 a0003c0003t0029g0018 |
3 | HG00741.hp1 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1367+4510C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014960 | |||||||
| chr12:117014961 | A | C | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4511A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014961 | |||||||
| chr12:117014980 | T | A | 1 | a0001c0001t0004g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4530T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014980 | |||||||
| chr12:117014985 | G | A | 1 | a0011c0015t0003g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1367+4535G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014985 | |||||||
| chr12:117015090 | C | T | 1 | a0002c0002t0030g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1367+4640C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015090 | |||||||
| chr12:117015117 | A | G | 44 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(41): Show |
47 | HG00323.hp1 HG00642.hp2 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.1367+4667A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015117 | |||||||
| chr12:117015417 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+4967A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015417 | |||||||
| chr12:117015494 | G | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+5044G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015494 | |||||||
| chr12:117015726 | T | C | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1367+5276T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015726 | |||||||
| chr12:117015752 | TC | T | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+5304delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117015752 | ||||||
| chr12:117015777 | A | G | 2 | a0001c0001t0004g0037 a0001c0001t0004g0045 |
2 | NA18947.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1367+5327A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015777 | |||||||
| chr12:117015778 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1367+5328C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015778 | |||||||
| chr12:117015788 | T | G | 8 | a0002c0002t0002g0003 a0002c0002t0002g0089 a0002c0002t0002g0090 others(5): Show |
9 | HG01175.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367+5338T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015788 | |||||||
| chr12:117016110 | A | G | 1 | a0002c0002t0005g0092 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1367+5660A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016110 | |||||||
| chr12:117016165 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+5715A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016165 | |||||||
| chr12:117016336 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1367+5886C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016336 | |||||||
| chr12:117016383 | C | T | 2 | a0006c0010t0013g0108 a0006c0010t0013g0109 |
2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1367+5933C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016383 | |||||||
| chr12:117016492 | A | AT | 88 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(85): Show |
91 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1367+6049dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117016492 | ||||||
| chr12:117016642 | G | GT | 23 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0004g0031 others(20): Show |
23 | HG00423.hp2 HG00544.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1367+6207dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117016642 | ||||||
| chr12:117016642 | GT | G | 19 | a0001c0001t0001g0169 a0002c0002t0002g0093 a0002c0002t0002g0096 others(16): Show |
20 | HG00741.hp1 HG01192.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1367+6207delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117016642 | ||||||
| chr12:117016646 | T | G | 1 | a0005c0007t0007g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1367+6196T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016646 | |||||||
| chr12:117016672 | T | C | 8 | a0001c0001t0004g0032 a0001c0001t0004g0037 a0001c0001t0004g0038 others(5): Show |
8 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+6222T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016672 | |||||||
| chr12:117017560 | A | G | 157 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(154): Show |
162 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1368-6587A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117017560 | |||||||
| chr12:117017678 | A | T | 3 | a0002c0002t0002g0085 a0002c0002t0002g0119 a0002c0002t0002g0121 |
3 | NA18950.hp1 NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1368-6469A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117017678 | |||||||
| chr12:117017987 | C | T | 4 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-6160C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117017987 | |||||||
| chr12:117018129 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1368-6018T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117018129 | |||||||
| chr12:117018303 | A | G | 1 | a0001c0006t0001g0245 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1368-5844A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117018303 | |||||||
| chr12:117018606 | A | AGCTT | 120 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(117): Show |
123 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1368-5541_1368-554 others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117018606 | |||||||
| chr12:117018633 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1368-5514A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117018633 | |||||||
| chr12:117018954 | G | GA | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-5189dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117018954 | ||||||
| chr12:117019015 | T | C | 2 | a0002c0002t0011g0082 a0002c0002t0011g0147 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1368-5132T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019015 | |||||||
| chr12:117019018 | A | C | 145 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(142): Show |
150 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1368-5129A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019018 | |||||||
| chr12:117019030 | G | A | 1 | a0002c0002t0002g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1368-5117G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019030 | |||||||
| chr12:117019219 | T | G | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1368-4928T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019219 | |||||||
| chr12:117019258 | G | A | 1 | a0002c0002t0024g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1368-4889G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019258 | |||||||
| chr12:117019302 | C | T | 1 | a0002c0002t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1368-4845C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019302 | |||||||
| chr12:117019420 | C | T | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1368-4727C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019420 | |||||||
| chr12:117019434 | T | C | 1 | a0002c0002t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1368-4713T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019434 | |||||||
| chr12:117019474 | T | C | 1 | a0001c0001t0003g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1368-4673T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019474 | |||||||
| chr12:117019667 | G | T | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-4480G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019667 | |||||||
| chr12:117019698 | C | T | 2 | a0003c0020t0020g0081 a0009c0016t0003g0029 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1368-4449C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019698 | |||||||
| chr12:117019736 | T | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-4411T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019736 | |||||||
| chr12:117019958 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-4189A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019958 | |||||||
| chr12:117020091 | G | A | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1368-4056G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020091 | |||||||
| chr12:117020106 | A | G | 1 | a0002c0002t0002g0074 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1368-4041A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020106 | |||||||
| chr12:117020220 | A | G | 1 | a0002c0002t0002g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1368-3927A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020220 | |||||||
| chr12:117020289 | C | G | 3 | a0003c0003t0003g0166 a0003c0003t0003g0192 a0010c0019t0003g0193 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1368-3858C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020289 | |||||||
| chr12:117020328 | A | AT | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-3813dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117020328 | ||||||
| chr12:117020426 | T | C | 1 | a0003c0020t0020g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1368-3721T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020426 | |||||||
| chr12:117020451 | C | T | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1368-3696C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020451 | |||||||
| chr12:117020456 | G | A | 1 | a0002c0002t0005g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1368-3691G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020456 | |||||||
| chr12:117020503 | T | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-3644T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020503 | |||||||
| chr12:117020508 | C | A | 1 | a0011c0015t0003g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1368-3639C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020508 | |||||||
| chr12:117020584 | C | T | 11 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(8): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1368-3563C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020584 | |||||||
| chr12:117020636 | A | G | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1368-3511A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020636 | |||||||
| chr12:117020679 | C | T | 1 | a0001c0001t0003g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1368-3468C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020679 | |||||||
| chr12:117020997 | C | T | 17 | a0002c0002t0002g0086 a0002c0002t0002g0088 a0003c0003t0006g0004 others(14): Show |
18 | HG00741.hp1 HG02109.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1368-3150C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020997 | |||||||
| chr12:117020999 | G | T | 2 | a0001c0001t0004g0037 a0001c0001t0004g0045 |
2 | NA18947.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1368-3148G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020999 | |||||||
| chr12:117021054 | G | A | 142 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(139): Show |
147 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1368-3093G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021054 | |||||||
| chr12:117021158 | G | C | 13 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(10): Show |
14 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1368-2989G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021158 | |||||||
| chr12:117021240 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1368-2907C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021240 | |||||||
| chr12:117021393 | G | A | 3 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0007c0012t0018g0012 |
3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1368-2754G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021393 | |||||||
| chr12:117021489 | AAT | A | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1368-2655_1368-265 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021489 | ||||||
| chr12:117021496 | T | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-2651T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021496 | |||||||
| chr12:117021581 | ATAGAG | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0052 |
3 | HG02622.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1368-2563_1368-255 others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021581 | ||||||
| chr12:117021583 | A | AGAG | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-2563_1368-256 others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021583 | ||||||
| chr12:117021592 | T | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-2555T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021592 | |||||||
| chr12:117021639 | A | AT | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-2503dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021639 | ||||||
| chr12:117021640 | T | C | 31 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(28): Show |
31 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1368-2507T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021640 | |||||||
| chr12:117021676 | G | A | 1 | a0001c0001t0004g0044 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1368-2471G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021676 | |||||||
| chr12:117021745 | A | AT | 13 | a0002c0002t0002g0150 a0002c0002t0008g0069 a0002c0002t0008g0083 others(10): Show |
14 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1368-2394dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021745 | ||||||
| chr12:117021805 | T | C | 9 | a0002c0002t0011g0082 a0002c0002t0011g0147 a0003c0003t0011g0010 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1368-2342T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021805 | |||||||
| chr12:117022003 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1368-2144C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022003 | |||||||
| chr12:117022134 | A | G | 13 | a0002c0002t0002g0150 a0002c0002t0008g0069 a0002c0002t0008g0083 others(10): Show |
14 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1368-2013A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022134 | |||||||
| chr12:117022272 | T | C | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1368-1875T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022272 | |||||||
| chr12:117022355 | T | TA | 20 | a0001c0001t0003g0148 a0001c0001t0004g0031 a0001c0001t0004g0032 others(17): Show |
20 | HG00544.hp1 HG02080.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1368-1777dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117022355 | ||||||
| chr12:117022355 | TA | T | 20 | a0001c0001t0001g0242 a0002c0002t0008g0069 a0002c0002t0008g0083 others(17): Show |
21 | HG00741.hp1 HG01074.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1368-1777delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117022355 | ||||||
| chr12:117022357 | A | T | 15 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(12): Show |
16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1368-1790A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022357 | |||||||
| chr12:117022358 | A | T | 1 | a0003c0003t0021g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1368-1789A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022358 | |||||||
| chr12:117022424 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0282 |
3 | HG02818.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1368-1723G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022424 | |||||||
| chr12:117022442 | C | T | 4 | a0002c0002t0009g0001 a0002c0002t0009g0060 a0002c0002t0009g0061 others(1): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-1705C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022442 | |||||||
| chr12:117022451 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1368-1696C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022451 | |||||||
| chr12:117022548 | G | A | 16 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 others(13): Show |
16 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.1368-1599G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022548 | |||||||
| chr12:117022614 | C | T | 1 | a0002c0002t0002g0121 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1368-1533C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022614 | |||||||
| chr12:117022656 | T | TA | 7 | a0003c0003t0010g0013 a0003c0003t0010g0014 a0003c0003t0010g0016 others(4): Show |
7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-1483dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117022656 | ||||||
| chr12:117022998 | C | T | 1 | a0002c0002t0002g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1368-1149C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022998 | |||||||
| chr12:117023036 | C | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0269 |
2 | HG02040.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1368-1111C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023036 | |||||||
| chr12:117023204 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1368-943A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023204 | |||||||
| chr12:117023247 | G | A | 1 | a0003c0021t0017g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1368-900G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023247 | |||||||
| chr12:117023279 | C | T | 1 | a0002c0002t0005g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1368-868C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023279 | |||||||
| chr12:117023545 | T | TG | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-598dupG | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117023545 | ||||||
| chr12:117023613 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1368-534C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023613 | |||||||
| chr12:117023668 | C | T | 1 | a0002c0002t0002g0053 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1368-479C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023668 | |||||||
| chr12:117023970 | G | A | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1368-177G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023970 | |||||||
| chr12:117024109 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1368-38C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117024109 | |||||||
| chr12:117024112 | C | T | 2 | a0001c0001t0003g0198 a0001c0001t0003g0213 |
2 | HG00423.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1368-35C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117024112 | |||||||
| chr12:117024133 | C | T | 27 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(24): Show |
29 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1368-14C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117024133 | |||||||
| chr12:117024325 | G | C | 1 | a0003c0003t0011g0010 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.1541+5G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024325 | |||||||
| chr12:117024363 | C | G | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1541+43C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024363 | |||||||
| chr12:117024479 | C | T | 1 | a0002c0002t0002g0139 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1541+159C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024479 | |||||||
| chr12:117024718 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1541+398C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024718 | |||||||
| chr12:117024734 | G | T | 1 | a0001c0001t0003g0199 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1541+414G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024734 | |||||||
| chr12:117024777 | C | T | 39 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(36): Show |
40 | HG00323.hp1 HG00642.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.1541+457C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024777 | |||||||
| chr12:117024847 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1541+527G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024847 | |||||||
| chr12:117024939 | C | T | 2 | a0003c0003t0012g0021 a0003c0003t0012g0022 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1541+619C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024939 | |||||||
| chr12:117024980 | G | A | 122 | a0001c0001t0001g0231 a0002c0002t0002g0003 a0002c0002t0002g0030 others(119): Show |
127 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1541+660G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024980 | |||||||
| chr12:117024986 | C | CCTAA | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1541+669_1541+672d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117024986 | ||||||
| chr12:117025128 | G | A | 1 | a0001c0006t0001g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1541+808G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025128 | |||||||
| chr12:117025130 | G | A | 1 | a0002c0002t0008g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1541+810G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025130 | |||||||
| chr12:117025146 | G | C | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1541+826G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025146 | |||||||
| chr12:117025251 | G | A | 1 | a0003c0003t0021g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1541+931G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025251 | |||||||
| chr12:117025354 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1541+1034G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025354 | |||||||
| chr12:117025393 | A | T | 12 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(9): Show |
12 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1541+1073A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025393 | |||||||
| chr12:117025399 | G | C | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1541+1079G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025399 | |||||||
| chr12:117025494 | G | A | 3 | a0003c0003t0006g0006 a0003c0003t0006g0008 a0003c0003t0006g0009 |
3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1541+1174G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025494 | |||||||
| chr12:117025512 | A | G | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1541+1192A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025512 | |||||||
| chr12:117025570 | T | G | 1 | a0001c0001t0004g0041 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1541+1250T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025570 | |||||||
| chr12:117025585 | A | G | 159 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(156): Show |
164 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1541+1265A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025585 | |||||||
| chr12:117025610 | A | G | 6 | a0002c0002t0011g0082 a0002c0002t0011g0147 a0003c0003t0011g0010 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1541+1290A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025610 | |||||||
| chr12:117025801 | C | CCATCCA | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1541+1482_1541+148 others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117025801 | ||||||
| chr12:117025965 | C | T | 2 | a0002c0008t0002g0067 a0002c0008t0002g0068 |
2 | HG02148.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1542-1429C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025965 | |||||||
| chr12:117026101 | T | C | 96 | a0001c0001t0034g0172 a0002c0002t0002g0003 a0002c0002t0002g0030 others(93): Show |
99 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1542-1293T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026101 | |||||||
| chr12:117026127 | C | T | 13 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(10): Show |
13 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1542-1267C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026127 | |||||||
| chr12:117026181 | GTCAGTCC others(90): Show |
G | 20 | a0001c0001t0001g0189 a0002c0002t0001g0146 a0002c0002t0002g0145 others(17): Show |
21 | HG00741.hp1 HG01074.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.1542-1072_1542-976 others(100): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026181 | ||||||
| chr12:117026246 | C | T | 3 | a0003c0003t0012g0020 a0003c0003t0012g0021 a0003c0003t0012g0022 |
3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1542-1148C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026246 | |||||||
| chr12:117026276 | C | G | 2 | a0001c0001t0003g0154 a0001c0001t0003g0156 |
2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1542-1118C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026276 | |||||||
| chr12:117026322 | CCCCGGGT others(90): Show |
C | 2 | a0003c0003t0011g0010 a0003c0003t0011g0011 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1542-1016_1542-920 others(100): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026322 | ||||||
| chr12:117026384 | C | T | 14 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(11): Show |
15 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-1010C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026384 | |||||||
| chr12:117026419 | T | C | 3 | a0002c0002t0011g0082 a0002c0002t0011g0147 a0007c0012t0018g0012 |
3 | HG02055.hp2 HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1542-975T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026419 | |||||||
| chr12:117026509 | C | CT | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1542-883dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026509 | ||||||
| chr12:117026578 | A | G | 15 | a0002c0002t0002g0095 a0002c0002t0002g0104 a0002c0002t0002g0105 others(12): Show |
15 | HG00323.hp1 HG00642.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-816A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026578 | |||||||
| chr12:117026608 | C | CCAACAGA others(6): Show |
182 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(179): Show |
187 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.1542-784_1542-783i others(15): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026608 | ||||||
| chr12:117026638 | C | CACTT | 4 | a0001c0001t0003g0047 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1542-754_1542-751d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026638 | ||||||
| chr12:117026645 | C | T | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1542-749C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026645 | |||||||
| chr12:117026814 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1542-580G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026814 | |||||||
| chr12:117026869 | A | G | 14 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(11): Show |
15 | HG01106.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1542-525A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026869 | |||||||
| chr12:117026880 | A | G | 71 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(68): Show |
76 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.1542-514A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026880 | |||||||
| chr12:117026965 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1542-429G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026965 | |||||||
| chr12:117027137 | T | C | 1 | a0002c0002t0002g0053 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1542-257T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027137 | |||||||
| chr12:117027164 | C | T | 12 | a0002c0002t0008g0069 a0002c0002t0008g0083 a0002c0002t0008g0110 others(9): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1542-230C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027164 | |||||||
| chr12:117027165 | G | A | 46 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(43): Show |
46 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1542-229G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027165 | |||||||
| chr12:117027189 | G | A | 2 | a0003c0003t0003g0166 a0003c0003t0003g0192 |
2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1542-205G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027189 | |||||||
| chr12:117027335 | G | A | 4 | a0003c0003t0011g0010 a0003c0003t0011g0011 a0003c0021t0017g0005 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1542-59G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027335 | |||||||
| chr12:117027572 | C | A | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1652+68C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027572 | |||||||
| chr12:117027577 | G | A | 1 | a0002c0002t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1652+73G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027577 | |||||||
| chr12:117027648 | G | A | 1 | a0002c0002t0005g0092 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1652+144G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027648 | |||||||
| chr12:117027719 | G | A | 14 | a0003c0003t0006g0004 a0003c0003t0006g0006 a0003c0003t0006g0008 others(11): Show |
15 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1652+215G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027719 | |||||||
| chr12:117027757 | G | C | 45 | a0001c0001t0003g0191 a0001c0001t0003g0230 a0002c0002t0002g0072 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1652+253G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027757 | |||||||
| chr12:117027828 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1653-200C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027828 | |||||||
| chr12:117027907 | G | A | 3 | a0002c0002t0005g0064 a0002c0002t0005g0100 a0002c0002t0005g0134 |
3 | HG01256.hp2 HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1653-121G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027907 | |||||||
| chr12:117027909 | G | C | 77 | a0002c0002t0002g0003 a0002c0002t0002g0030 a0002c0002t0002g0053 others(74): Show |
82 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.1653-119G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027909 |