Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80204 |
| ensemblid | ENSG00000138081.22 |
| hgncid | 13590 |
| symbol | FBXO11 |
| name | F-box protein 11 |
| refseq_nuc | NM_001190274.2 |
| refseq_prot | NP_001177203.1 |
| ensembl_nuc | ENST00000403359.8 |
| ensembl_prot | ENSP00000384823.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 47806920 |
| end | 47906498 |
| strand | - |
| ver | v1.2 |
| region | chr2:47806920-47906498 |
| region5000 | chr2:47801920-47911498 |
| regionname0 | FBXO11_chr2_47806920_47906498 |
| regionname5000 | FBXO11_chr2_47801920_47911498 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 927 | 307 | 82 | 58 | 117 | 14 | 34 | 91 | FBXO11_chr2_47801920_47911498 | FBXO11 | MNSVR others(922): Show |
chr2 | 47801920 | 47911498 |
| a0002 | 0/0 | 928 | 3 | 1 | 1 | 1 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | MNSVR others(923): Show |
chr2 | 47801920 | 47911498 |
| a0003 | 0/0 | 927 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | MNSVR others(922): Show |
chr2 | 47801920 | 47911498 |
| a0004 | 0/0 | 922 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | MNSVR others(917): Show |
chr2 | 47801920 | 47911498 |
| a0005 | 0/0 | 927 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | MNSVR others(922): Show |
chr2 | 47801920 | 47911498 |
| a0006 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | MNSVR others(922): Show |
chr2 | 47801920 | 47911498 |
| a0007 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | MNSVR others(922): Show |
chr2 | 47801920 | 47911498 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2781 | 297 | 74 | 56 | 117 | 14 | 34 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2776): Show |
chr2 | 47801920 | 47911498 | ||
| a0001c0002 | 0/0 | 2781 | 9 | 8 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2776): Show |
chr2 | 47801920 | 47911498 | ||
| a0001c0007 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2776): Show |
chr2 | 47801920 | 47911498 | ||
| a0002c0003 | 0/0 | 2784 | 3 | 1 | 1 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2779): Show |
chr2 | 47801920 | 47911498 | ||
| a0003c0004 | 0/0 | 2781 | 3 | 3 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2776): Show |
chr2 | 47801920 | 47911498 | ||
| a0004c0005 | 0/0 | 2766 | 2 | 1 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2761): Show |
chr2 | 47801920 | 47911498 | ||
| a0005c0006 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2776): Show |
chr2 | 47801920 | 47911498 | ||
| a0006c0008 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2776): Show |
chr2 | 47801920 | 47911498 | ||
| a0007c0009 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | ATGAA others(2776): Show |
chr2 | 47801920 | 47911498 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4759 | 203 | 51 | 31 | 84 | 12 | 25 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0002 | 1/1 | 4760 | 69 | 11 | 24 | 22 | 2 | 8 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0003 | 0/0 | 4760 | 6 | 6 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0004 | 0/0 | 4765 | 3 | 0 | 0 | 3 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4760): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0005 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4782): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0006 | 0/0 | 4759 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0007 | 0/0 | 4759 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0008 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0009 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0010 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0011 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0012 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0013 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0014 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0015 | 0/0 | 4759 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0016 | 0/0 | 4775 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4770): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0017 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0018 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0019 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0001c0001t0020 | 0/0 | 4760 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0001c0002t0002 | 0/0 | 4760 | 9 | 8 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0001c0007t0002 | 0/0 | 4760 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0002c0003t0001 | 0/0 | 4762 | 3 | 1 | 1 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4757): Show |
chr2 | 47801920 | 47911498 |
| a0003c0004t0002 | 0/0 | 4760 | 3 | 3 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4755): Show |
chr2 | 47801920 | 47911498 |
| a0004c0005t0002 | 0/0 | 4745 | 2 | 1 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4740): Show |
chr2 | 47801920 | 47911498 |
| a0005c0006t0001 | 0/0 | 4759 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0006c0008t0001 | 0/0 | 4759 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| a0007c0009t0001 | 0/0 | 4759 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | GGGCG others(4754): Show |
chr2 | 47801920 | 47911498 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0008g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0010g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0011g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0013g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0014g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0015g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0016g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0017g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0018g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0019g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0001t0020g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0002t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0001c0007t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0002c0003t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0002c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0003c0004t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0003c0004t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0003c0004t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0004c0005t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0004c0005t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0005c0006t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0006c0008t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| a0007c0009t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0238 | EUR | FIN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | FIN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00738 | hp2 | a0001 | c0007 | t0002 | g0239 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0013 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0123 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01169 | hp2 | a0001 | c0001 | t0016 | g0308 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0247 | EUR | IBS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01884 | hp1 | a0003 | c0004 | t0002 | g0203 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0201 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01993 | hp2 | a0005 | c0006 | t0001 | g0051 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02135 | hp1 | a0001 | c0001 | t0011 | g0107 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02145 | hp2 | a0001 | c0001 | t0020 | g0312 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CDX | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CDX | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02165 | hp2 | a0006 | c0008 | t0001 | g0304 | EAS | CDX | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02258 | hp2 | a0007 | c0009 | t0001 | g0305 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02451 | hp1 | a0004 | c0005 | t0002 | g0307 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02523 | hp1 | a0004 | c0005 | t0002 | g0306 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02723 | hp2 | a0001 | c0001 | t0014 | g0127 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02896 | hp1 | a0003 | c0004 | t0002 | g0204 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0197 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0298 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0287 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03516 | hp1 | a0003 | c0004 | t0002 | g0195 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | GWD | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0009 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | BEB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | CHB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0217 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18952 | hp2 | a0001 | c0001 | t0012 | g0175 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18954 | hp1 | a0001 | c0001 | t0017 | g0309 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18964 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18965 | hp1 | a0001 | c0001 | t0018 | g0310 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18965 | hp2 | a0001 | c0001 | t0019 | g0311 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0211 | AFR | LWK | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | ASW | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0196 | AFR | MSL | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | USA | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | USA | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | LWK | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0291 | REF | REF | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0061 | REF | REF | FBXO11_chr2_47801920_47911498 | FBXO11 | chr2 | 47801920 | 47911498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47806922 | A | G | 1 | a0001 | 1 | HG03453.hp2 | splice_region_variant | LOW | c.*1196T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | chr2 | 47806922 | |||||||
| chr2:47832769 | C | T | 1 | a0005 | 1 | HG01993.hp2 | missense_variant&splice_region_variant | MODERATE | c.1153G>A | p.Val385Ile | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 9/23 | 1931/4760 | 1153/2784 | 385/927 | chr2 | 47832769 | |||
| chr2:47839485 | T | A | 1 | a0003 | 3 | HG01884.hp1 HG02896.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.376A>T | p.Thr126Ser | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 3/23 | 1154/4760 | 376/2784 | 126/927 | chr2 | 47839485 | |||
| chr2:47905551 | G | GGCT | 1 | a0002 | 3 | HG00741.hp2 NA19091.hp1 NA20300.hp2 |
conservative_inframe_insertion | MODERATE | c.167_169dupAGC | p.Gln56dup | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 947/4760 | 169/2784 | 57/927 | chr2 | 47905551 | |||
| chr2:47905569 | T | G | 1 | a0007 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.152A>C | p.Gln51Pro | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 930/4760 | 152/2784 | 51/927 | chr2 | 47905569 | |||
| chr2:47905572 | T | G | 2 | a0006 a0007 |
2 | HG02165.hp2 HG02258.hp2 |
missense_variant | MODERATE | c.149A>C | p.Gln50Pro | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 927/4760 | 149/2784 | 50/927 | chr2 | 47905572 | |||
| chr2:47905586 | AGGCTGCT others(8): Show |
A | 1 | a0004 | 2 | HG02451.hp1 HG02523.hp1 |
disruptive_inframe_deletion | MODERATE | c.120_134delGCCCCAGC others(7): Show |
p.Pro41_Pro45del | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 912/4760 | 120/2784 | 40/927 | chr2 | 47905586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47823181 | T | C | 1 | a0001c0002 | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
synonymous_variant | LOW | c.1578A>G | p.Ala526Ala | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/23 | 2356/4760 | 1578/2784 | 526/927 | chr2 | 47823181 | |||
| chr2:47823196 | A | G | 1 | a0001c0007 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1563T>C | p.Tyr521Tyr | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/23 | 2341/4760 | 1563/2784 | 521/927 | chr2 | 47823196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47807347 | G | C | 1 | a0001c0001t0011 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*771C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 771 | chr2 | 47807347 | ||||||
| chr2:47807549 | G | A | 1 | a0001c0001t0014 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*569C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 569 | chr2 | 47807549 | ||||||
| chr2:47807657 | G | A | 1 | a0001c0001t0012 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 461 | chr2 | 47807657 | ||||||
| chr2:47807667 | TA | T | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(14): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*450delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 450 | chr2 | 47807667 | ||||||
| chr2:47807682 | A | C | 1 | a0001c0001t0010 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 436 | chr2 | 47807682 | ||||||
| chr2:47807777 | T | C | 1 | a0001c0001t0015 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 341 | chr2 | 47807777 | ||||||
| chr2:47807848 | T | C | 1 | a0001c0001t0003 | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*270A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 23/23 | 270 | chr2 | 47807848 | ||||||
| chr2:47905758 | A | ACACACG | 1 | a0001c0001t0004 | 3 | HG02135.hp2 HG02523.hp2 NA18982.hp2 |
5_prime_UTR_variant | MODIFIER | c.-44_-39dupCGTGTG | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 39 | chr2 | 47905758 | ||||||
| chr2:47905786 | G | A | 1 | a0001c0001t0020 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 66 | chr2 | 47905786 | ||||||
| chr2:47905810 | T | TGGGAGAG others(9): Show |
1 | a0001c0001t0016 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106_-91dupTCCTCCC others(9): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 91 | chr2 | 47905810 | ||||||
| chr2:47905818 | G | T | 1 | a0001c0001t0009 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 98 | chr2 | 47905818 | ||||||
| chr2:47905885 | G | A | 1 | a0001c0001t0017 | 1 | NA18954.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-165C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | chr2 | 47905885 | |||||||
| chr2:47906100 | G | A | 1 | a0001c0001t0018 | 1 | NA18965.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-380C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | chr2 | 47906100 | |||||||
| chr2:47906165 | G | A | 1 | a0001c0001t0019 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-445C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 445 | chr2 | 47906165 | ||||||
| chr2:47906215 | C | T | 1 | a0001c0001t0008 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-495G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 495 | chr2 | 47906215 | ||||||
| chr2:47906314 | C | G | 1 | a0001c0001t0007 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-594G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 594 | chr2 | 47906314 | ||||||
| chr2:47906326 | C | T | 1 | a0001c0001t0006 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-606G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 606 | chr2 | 47906326 | ||||||
| chr2:47906327 | G | C | 1 | a0001c0001t0020 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-607C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 607 | chr2 | 47906327 | ||||||
| chr2:47906331 | A | AAGGGGAA others(21): Show |
1 | a0001c0001t0005 | 1 | NA19057.hp1 | 5_prime_UTR_variant | MODIFIER | c.-639_-612dupATCTCC others(22): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/23 | 612 | chr2 | 47906331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47808492 | TTTATA | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2556-70_2556-66del others(5): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808492 | |||||||
| chr2:47808503 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2556-76G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808503 | |||||||
| chr2:47808534 | A | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(119): Show |
124 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2556-107T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808534 | |||||||
| chr2:47808679 | C | G | 6 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2556-252G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808679 | |||||||
| chr2:47808684 | G | C | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.2556-257C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808684 | |||||||
| chr2:47808735 | A | G | 6 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2556-308T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808735 | |||||||
| chr2:47808744 | G | GA | 9 | a0001c0002t0002g0123 a0001c0002t0002g0196 a0001c0002t0002g0197 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2556-318dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808744 | |||||||
| chr2:47808854 | T | G | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2555+304A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808854 | |||||||
| chr2:47808860 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2555+298A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808860 | |||||||
| chr2:47808943 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2555+215G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808943 | |||||||
| chr2:47808991 | C | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2555+167G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47808991 | |||||||
| chr2:47809030 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2555+128T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47809030 | |||||||
| chr2:47809048 | A | G | 1 | a0003c0004t0002g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2555+110T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47809048 | |||||||
| chr2:47809105 | A | G | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 |
3 | HG01261.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2555+53T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 21/22 | chr2 | 47809105 | |||||||
| chr2:47809440 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2446+160A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 20/22 | chr2 | 47809440 | |||||||
| chr2:47809748 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2339-41T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809748 | |||||||
| chr2:47809772 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2339-65T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809772 | |||||||
| chr2:47809793 | T | G | 1 | a0003c0004t0002g0204 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2339-86A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809793 | |||||||
| chr2:47809860 | C | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0005g0007 |
3 | HG00609.hp2 HG02080.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2339-153G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809860 | |||||||
| chr2:47809903 | A | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0122 |
3 | HG02055.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2339-196T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809903 | |||||||
| chr2:47809914 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2339-207C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809914 | |||||||
| chr2:47809942 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2339-235T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47809942 | |||||||
| chr2:47810103 | T | C | 1 | a0001c0001t0017g0309 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2338+213A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47810103 | |||||||
| chr2:47810171 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2338+145G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 19/22 | chr2 | 47810171 | |||||||
| chr2:47810454 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0073 others(4): Show |
7 | HG00609.hp2 HG02027.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.2228-28C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810454 | |||||||
| chr2:47810480 | C | G | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2228-54G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810480 | |||||||
| chr2:47810650 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2228-224G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810650 | |||||||
| chr2:47810683 | T | G | 2 | a0001c0001t0002g0095 a0001c0001t0002g0292 |
2 | NA19007.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2228-257A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810683 | |||||||
| chr2:47810766 | C | T | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2228-340G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810766 | |||||||
| chr2:47810771 | A | G | 11 | a0001c0001t0002g0033 a0001c0001t0002g0046 a0001c0001t0002g0180 others(8): Show |
11 | HG00280.hp1 HG00738.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2228-345T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810771 | |||||||
| chr2:47810831 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2228-405T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810831 | |||||||
| chr2:47810927 | T | C | 1 | a0001c0001t0013g0287 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2228-501A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47810927 | |||||||
| chr2:47811003 | A | C | 1 | a0001c0001t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2228-577T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811003 | |||||||
| chr2:47811102 | C | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0001g0091 others(4): Show |
7 | NA18971.hp2 NA19010.hp2 NA19066.hp1 others(4): Show |
intron_variant | MODIFIER | c.2228-676G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811102 | |||||||
| chr2:47811143 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2228-717T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811143 | |||||||
| chr2:47811144 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2228-718A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811144 | |||||||
| chr2:47811145 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2228-719A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811145 | |||||||
| chr2:47811146 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2228-720T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811146 | |||||||
| chr2:47811192 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
42 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.2228-766C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811192 | |||||||
| chr2:47811207 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2228-781C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811207 | |||||||
| chr2:47811318 | G | C | 1 | a0001c0001t0001g0176 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2228-892C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811318 | |||||||
| chr2:47811640 | T | C | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.2228-1214A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811640 | |||||||
| chr2:47811744 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2228-1318G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811744 | |||||||
| chr2:47811798 | C | A | 2 | a0001c0001t0002g0261 a0001c0001t0013g0287 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2228-1372G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811798 | |||||||
| chr2:47811805 | A | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.2228-1379T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811805 | |||||||
| chr2:47811809 | C | T | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.2228-1383G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811809 | |||||||
| chr2:47811905 | T | C | 29 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(26): Show |
29 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2227+1329A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811905 | |||||||
| chr2:47811913 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2227+1321C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811913 | |||||||
| chr2:47811945 | C | T | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2227+1289G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811945 | |||||||
| chr2:47811951 | C | A | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2227+1283G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811951 | |||||||
| chr2:47811982 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2227+1252A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47811982 | |||||||
| chr2:47812084 | T | G | 38 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(35): Show |
38 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2227+1150A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812084 | |||||||
| chr2:47812088 | A | C | 9 | a0001c0002t0002g0123 a0001c0002t0002g0196 a0001c0002t0002g0197 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2227+1146T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812088 | |||||||
| chr2:47812112 | CCT | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2227+1120_2227+112 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812112 | |||||||
| chr2:47812173 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2227+1061A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812173 | |||||||
| chr2:47812345 | T | G | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2227+889A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812345 | |||||||
| chr2:47812480 | A | G | 1 | a0001c0001t0002g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2227+754T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812480 | |||||||
| chr2:47812543 | A | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0153 |
2 | NA18953.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.2227+691T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812543 | |||||||
| chr2:47812605 | C | T | 36 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(33): Show |
36 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2227+629G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812605 | |||||||
| chr2:47812683 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2227+551C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812683 | |||||||
| chr2:47812789 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2227+445G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812789 | |||||||
| chr2:47812891 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2227+343A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47812891 | |||||||
| chr2:47813114 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2227+120T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47813114 | |||||||
| chr2:47813146 | A | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0080 a0001c0001t0001g0103 others(4): Show |
7 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.2227+88T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 18/22 | chr2 | 47813146 | |||||||
| chr2:47813425 | A | ATTT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0086 a0001c0001t0001g0088 others(4): Show |
7 | HG00280.hp1 HG02071.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.2084-51_2084-49dup others(3): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTT | 74 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0037 others(71): Show |
76 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2084-52_2084-49dup others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTT | 13 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0116 others(10): Show |
13 | HG01109.hp1 HG01346.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2084-53_2084-49dup others(5): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(2): Show |
34 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
35 | HG00099.hp1 HG00621.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2084-57_2084-49dup others(9): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(3): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0049 others(47): Show |
51 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.2084-58_2084-49dup others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(4): Show |
19 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0101 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2084-59_2084-49dup others(11): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(5): Show |
11 | a0001c0001t0001g0068 a0001c0001t0001g0176 a0001c0001t0001g0192 others(8): Show |
11 | HG00738.hp1 HG01884.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2084-60_2084-49dup others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(6): Show |
4 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(1): Show |
4 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2084-61_2084-49dup others(13): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0185 a0001c0001t0001g0290 a0001c0001t0003g0232 |
3 | HG02145.hp1 HG02630.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2084-62_2084-49dup others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(8): Show |
6 | a0001c0001t0001g0237 a0001c0001t0002g0167 a0001c0001t0002g0171 others(3): Show |
6 | HG02451.hp1 HG02897.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2084-63_2084-49dup others(15): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(9): Show |
5 | a0001c0001t0001g0229 a0001c0002t0002g0123 a0001c0002t0002g0198 others(2): Show |
5 | HG01109.hp2 HG01257.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2084-64_2084-49dup others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(10): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0137 a0001c0001t0001g0225 others(8): Show |
12 | HG00280.hp2 HG01070.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2084-65_2084-49dup others(17): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(11): Show |
3 | a0001c0001t0001g0227 a0001c0001t0003g0300 a0001c0002t0002g0202 |
3 | HG02735.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2084-66_2084-49dup others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0015g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2084-68_2084-49dup others(20): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2084-69_2084-49dup others(21): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | A | ATTTTTTT others(20): Show |
1 | a0001c0001t0003g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2084-49_2084-48ins others(27): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813425 | ATTTT | A | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2084-52_2084-49del others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813425 | |||||||
| chr2:47813519 | C | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2084-142G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813519 | |||||||
| chr2:47813560 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2084-183A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813560 | |||||||
| chr2:47813564 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2084-187A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813564 | |||||||
| chr2:47813645 | C | T | 35 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(32): Show |
35 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2083+146G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813645 | |||||||
| chr2:47813667 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0118 |
2 | NA18966.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2083+124C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813667 | |||||||
| chr2:47813728 | C | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(4): Show |
7 | HG01433.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2083+63G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813728 | |||||||
| chr2:47813765 | G | GA | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.2083+25dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 17/22 | chr2 | 47813765 | |||||||
| chr2:47813914 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2007-47G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47813914 | |||||||
| chr2:47814235 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2007-368G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814235 | |||||||
| chr2:47814238 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.2007-371T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814238 | |||||||
| chr2:47814242 | A | G | 4 | a0001c0001t0003g0232 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2007-375T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814242 | |||||||
| chr2:47814247 | T | C | 12 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0138 others(9): Show |
12 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2007-380A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814247 | |||||||
| chr2:47814255 | C | T | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0151 others(2): Show |
5 | NA18953.hp2 NA18979.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.2007-388G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814255 | |||||||
| chr2:47814333 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2007-466C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814333 | |||||||
| chr2:47814373 | C | CT | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2007-507dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814373 | |||||||
| chr2:47814373 | C | CTT | 14 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0189 others(11): Show |
14 | HG01346.hp1 HG02155.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.2007-508_2007-507d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814373 | |||||||
| chr2:47814411 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2007-544A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814411 | |||||||
| chr2:47814424 | C | CTGGAGT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2007-563_2007-558d others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814424 | |||||||
| chr2:47814523 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2007-656A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814523 | |||||||
| chr2:47814701 | G | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(11): Show |
14 | HG01433.hp1 HG01891.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2007-834C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814701 | |||||||
| chr2:47814906 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2007-1039G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814906 | |||||||
| chr2:47814909 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2007-1042G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814909 | |||||||
| chr2:47814919 | C | A | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0149 others(2): Show |
5 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.2007-1052G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47814919 | |||||||
| chr2:47815090 | T | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0293 |
3 | HG01243.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2007-1223A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815090 | |||||||
| chr2:47815099 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(13): Show |
17 | HG03492.hp2 HG03704.hp1 NA18942.hp2 others(14): Show |
intron_variant | MODIFIER | c.2007-1232T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815099 | |||||||
| chr2:47815221 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2007-1354A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815221 | |||||||
| chr2:47815433 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2007-1566A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815433 | |||||||
| chr2:47815641 | C | G | 1 | a0001c0001t0001g0088 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2007-1774G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815641 | |||||||
| chr2:47815778 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2007-1911A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815778 | |||||||
| chr2:47815908 | G | C | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2007-2041C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47815908 | |||||||
| chr2:47816079 | C | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2007-2212G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816079 | |||||||
| chr2:47816218 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 |
3 | HG01261.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2007-2351G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816218 | |||||||
| chr2:47816237 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2007-2370A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816237 | |||||||
| chr2:47816468 | A | G | 10 | a0001c0001t0002g0029 a0001c0001t0002g0056 a0001c0001t0002g0249 others(7): Show |
10 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.2006+2311T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816468 | |||||||
| chr2:47816589 | G | A | 2 | a0001c0001t0002g0235 a0001c0001t0002g0240 |
2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2006+2190C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816589 | |||||||
| chr2:47816598 | A | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2006+2181T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816598 | |||||||
| chr2:47816647 | C | CCA | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.2006+2130_2006+213 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816647 | |||||||
| chr2:47816745 | G | A | 1 | a0001c0002t0002g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2006+2034C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816745 | |||||||
| chr2:47816772 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2006+2007G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816772 | |||||||
| chr2:47816835 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2006+1944A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816835 | |||||||
| chr2:47816842 | T | G | 8 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0132 others(5): Show |
8 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.2006+1937A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816842 | |||||||
| chr2:47816906 | G | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2006+1873C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47816906 | |||||||
| chr2:47817021 | C | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0194 |
2 | HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2006+1758G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817021 | |||||||
| chr2:47817038 | G | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0194 |
2 | HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2006+1741C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817038 | |||||||
| chr2:47817292 | T | C | 1 | a0001c0001t0002g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2006+1487A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817292 | |||||||
| chr2:47817307 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2006+1472G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817307 | |||||||
| chr2:47817416 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2006+1363C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817416 | |||||||
| chr2:47817461 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2006+1318C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817461 | |||||||
| chr2:47817630 | C | T | 11 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(8): Show |
11 | NA18946.hp1 NA18953.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.2006+1149G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817630 | |||||||
| chr2:47817633 | C | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2006+1146G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817633 | |||||||
| chr2:47817918 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0084 others(7): Show |
11 | HG00544.hp2 HG00597.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.2006+861G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47817918 | |||||||
| chr2:47818056 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2006+723C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47818056 | |||||||
| chr2:47818111 | G | A | 5 | a0001c0001t0002g0056 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2006+668C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47818111 | |||||||
| chr2:47818151 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2006+628T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47818151 | |||||||
| chr2:47818167 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2006+612A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 16/22 | chr2 | 47818167 | |||||||
| chr2:47818873 | T | TA | 8 | a0001c0001t0001g0079 a0001c0001t0001g0237 a0001c0001t0002g0124 others(5): Show |
8 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1921-10dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 15/22 | chr2 | 47818873 | |||||||
| chr2:47819305 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1798-227G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819305 | |||||||
| chr2:47819364 | T | C | 12 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(9): Show |
12 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1798-286A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819364 | |||||||
| chr2:47819407 | C | T | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1798-329G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819407 | |||||||
| chr2:47819463 | G | A | 1 | a0001c0002t0002g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1798-385C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819463 | |||||||
| chr2:47819464 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1798-386A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819464 | |||||||
| chr2:47819504 | G | A | 1 | a0001c0001t0014g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1798-426C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819504 | |||||||
| chr2:47819558 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1798-480T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819558 | |||||||
| chr2:47819642 | G | T | 2 | a0001c0001t0002g0261 a0001c0001t0013g0287 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1798-564C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819642 | |||||||
| chr2:47819668 | A | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1798-590T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819668 | |||||||
| chr2:47819732 | T | C | 3 | a0001c0001t0001g0253 a0001c0001t0002g0005 a0001c0001t0016g0308 |
4 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1797+630A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819732 | |||||||
| chr2:47819746 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1797+616A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819746 | |||||||
| chr2:47819861 | T | C | 3 | a0001c0001t0001g0253 a0001c0001t0002g0005 a0001c0001t0016g0308 |
4 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1797+501A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819861 | |||||||
| chr2:47819880 | G | T | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1797+482C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47819880 | |||||||
| chr2:47820061 | C | A | 4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(1): Show |
4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797+301G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47820061 | |||||||
| chr2:47820070 | A | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797+292T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47820070 | |||||||
| chr2:47820196 | A | G | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1797+166T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47820196 | |||||||
| chr2:47820244 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1797+118G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 14/22 | chr2 | 47820244 | |||||||
| chr2:47820572 | G | A | 4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(1): Show |
4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1703-116C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47820572 | |||||||
| chr2:47820654 | C | T | 92 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(89): Show |
94 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1703-198G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47820654 | |||||||
| chr2:47820927 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0293 |
3 | HG01243.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1703-471A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47820927 | |||||||
| chr2:47821023 | A | C | 6 | a0001c0001t0001g0119 a0001c0001t0001g0273 a0001c0001t0001g0274 others(3): Show |
6 | HG01074.hp2 HG01891.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.1703-567T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821023 | |||||||
| chr2:47821145 | C | G | 12 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(9): Show |
12 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1703-689G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821145 | |||||||
| chr2:47821201 | G | A | 5 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1703-745C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821201 | |||||||
| chr2:47821201 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1703-745C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821201 | |||||||
| chr2:47821337 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1702+881C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821337 | |||||||
| chr2:47821365 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1702+853G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821365 | |||||||
| chr2:47821367 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1702+851A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821367 | |||||||
| chr2:47821407 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | NA18979.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1702+811C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821407 | |||||||
| chr2:47821440 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0216 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1702+778G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821440 | |||||||
| chr2:47821470 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1702+748G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821470 | |||||||
| chr2:47821567 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1702+651C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821567 | |||||||
| chr2:47821711 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1702+507C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821711 | |||||||
| chr2:47821734 | G | A | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702+484C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821734 | |||||||
| chr2:47821750 | A | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1702+468T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821750 | |||||||
| chr2:47821990 | G | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1702+228C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47821990 | |||||||
| chr2:47822136 | G | C | 1 | a0001c0001t0002g0272 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1702+82C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 13/22 | chr2 | 47822136 | |||||||
| chr2:47822423 | T | C | 6 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617-120A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822423 | |||||||
| chr2:47822576 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1617-273C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822576 | |||||||
| chr2:47822651 | C | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1617-348G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822651 | |||||||
| chr2:47822685 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1617-382A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822685 | |||||||
| chr2:47822761 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1616+382A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822761 | |||||||
| chr2:47822805 | A | G | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1616+338T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47822805 | |||||||
| chr2:47823057 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1616+86A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47823057 | |||||||
| chr2:47823088 | T | A | 2 | a0001c0001t0002g0259 a0001c0007t0002g0239 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1616+55A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 12/22 | chr2 | 47823088 | |||||||
| chr2:47823466 | C | CTT | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1399-107_1399-106i others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823466 | |||||||
| chr2:47823510 | C | G | 2 | a0001c0002t0002g0123 a0001c0002t0002g0298 |
2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1399-150G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823510 | |||||||
| chr2:47823547 | A | G | 17 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(14): Show |
17 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1399-187T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823547 | |||||||
| chr2:47823702 | G | A | 2 | a0001c0001t0002g0259 a0001c0007t0002g0239 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1399-342C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823702 | |||||||
| chr2:47823706 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-346A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823706 | |||||||
| chr2:47823763 | T | TA | 7 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(4): Show |
7 | HG01433.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399-404dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823763 | |||||||
| chr2:47823764 | A | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1399-404T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823764 | |||||||
| chr2:47823849 | A | AT | 7 | a0001c0001t0002g0245 a0001c0001t0003g0121 a0001c0001t0003g0135 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-490dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823849 | |||||||
| chr2:47823862 | T | A | 1 | a0001c0001t0001g0294 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1399-502A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823862 | |||||||
| chr2:47823904 | G | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-544C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47823904 | |||||||
| chr2:47824032 | C | G | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1399-672G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824032 | |||||||
| chr2:47824072 | A | G | 1 | a0001c0001t0009g0011 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1399-712T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824072 | |||||||
| chr2:47824324 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-964C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824324 | |||||||
| chr2:47824543 | T | A | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1399-1183A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824543 | |||||||
| chr2:47824610 | A | T | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1399-1250T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824610 | |||||||
| chr2:47824710 | G | A | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0193 others(1): Show |
4 | NA18971.hp1 NA18993.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-1350C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824710 | |||||||
| chr2:47824763 | T | G | 9 | a0001c0002t0002g0123 a0001c0002t0002g0196 a0001c0002t0002g0197 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1399-1403A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824763 | |||||||
| chr2:47824840 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1399-1480A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824840 | |||||||
| chr2:47824852 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0157 |
2 | HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1399-1492T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824852 | |||||||
| chr2:47824965 | A | G | 1 | a0001c0001t0011g0107 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1399-1605T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824965 | |||||||
| chr2:47824974 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1399-1614G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47824974 | |||||||
| chr2:47825026 | T | C | 12 | a0001c0001t0001g0068 a0001c0001t0001g0178 a0001c0001t0001g0179 others(9): Show |
12 | HG00438.hp1 HG02155.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.1399-1666A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825026 | |||||||
| chr2:47825057 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-1697A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825057 | |||||||
| chr2:47825091 | AT | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-1732delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825091 | |||||||
| chr2:47825143 | T | C | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1399-1783A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825143 | |||||||
| chr2:47825230 | GAAC | G | 4 | a0001c0001t0003g0232 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-1873_1399-187 others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825230 | |||||||
| chr2:47825270 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1399-1910A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825270 | |||||||
| chr2:47825412 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1399-2052A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825412 | |||||||
| chr2:47825513 | C | G | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-2153G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825513 | |||||||
| chr2:47825571 | C | CT | 30 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0044 others(27): Show |
31 | HG01074.hp2 HG01169.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1399-2212dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825571 | |||||||
| chr2:47825571 | CT | C | 17 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0063 others(14): Show |
17 | HG00738.hp1 HG01070.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1399-2212delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825571 | |||||||
| chr2:47825574 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0297 |
2 | HG02647.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1399-2214A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825574 | |||||||
| chr2:47825727 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1399-2367C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825727 | |||||||
| chr2:47825735 | C | G | 1 | a0001c0001t0002g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1399-2375G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825735 | |||||||
| chr2:47825758 | G | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1399-2398C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825758 | |||||||
| chr2:47825823 | C | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-2463G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825823 | |||||||
| chr2:47825840 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1399-2480C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825840 | |||||||
| chr2:47825881 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1399-2521T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825881 | |||||||
| chr2:47825967 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1399-2607G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47825967 | |||||||
| chr2:47826035 | TAA | T | 8 | a0001c0002t0002g0196 a0001c0002t0002g0197 a0001c0002t0002g0198 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1399-2677_1399-267 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826035 | |||||||
| chr2:47826037 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1399-2677T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826037 | |||||||
| chr2:47826050 | C | G | 18 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(15): Show |
18 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1399-2690G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826050 | |||||||
| chr2:47826068 | G | C | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1399-2708C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826068 | |||||||
| chr2:47826121 | C | T | 4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(1): Show |
4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-2761G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826121 | |||||||
| chr2:47826197 | T | C | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1399-2837A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826197 | |||||||
| chr2:47826206 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1399-2846G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826206 | |||||||
| chr2:47826225 | T | A | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1399-2865A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826225 | |||||||
| chr2:47826225 | T | G | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1399-2865A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826225 | |||||||
| chr2:47826236 | T | G | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1399-2876A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826236 | |||||||
| chr2:47826303 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1399-2943G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826303 | |||||||
| chr2:47826348 | C | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
10 | HG01433.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1399-2988G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826348 | |||||||
| chr2:47826495 | T | G | 1 | a0001c0001t0002g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1399-3135A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826495 | |||||||
| chr2:47826628 | G | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
18 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1399-3268C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826628 | |||||||
| chr2:47826640 | A | C | 1 | a0001c0001t0002g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1399-3280T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826640 | |||||||
| chr2:47826670 | T | C | 19 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0076 others(16): Show |
19 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1399-3310A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826670 | |||||||
| chr2:47826690 | A | AT | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-3331dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826690 | |||||||
| chr2:47826774 | T | G | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1399-3414A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826774 | |||||||
| chr2:47826786 | C | G | 19 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(16): Show |
19 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1399-3426G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826786 | |||||||
| chr2:47826992 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1399-3632G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47826992 | |||||||
| chr2:47827138 | A | C | 1 | a0001c0001t0002g0163 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1399-3778T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827138 | |||||||
| chr2:47827305 | TTTTG | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0118 a0001c0001t0002g0124 others(3): Show |
6 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1399-3949_1399-394 others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827305 | |||||||
| chr2:47827367 | C | T | 1 | a0001c0001t0011g0107 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1399-4007G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827367 | |||||||
| chr2:47827375 | C | T | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1399-4015G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827375 | |||||||
| chr2:47827390 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1399-4030A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827390 | |||||||
| chr2:47827393 | A | G | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1399-4033T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827393 | |||||||
| chr2:47827472 | A | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-4112T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827472 | |||||||
| chr2:47827498 | G | C | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1399-4138C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827498 | |||||||
| chr2:47827508 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1399-4148A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827508 | |||||||
| chr2:47827701 | A | AT | 17 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0073 others(14): Show |
17 | HG00609.hp1 HG00609.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1399-4342dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827701 | |||||||
| chr2:47827767 | G | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1399-4407C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827767 | |||||||
| chr2:47827866 | A | G | 2 | a0001c0002t0002g0123 a0001c0002t0002g0298 |
2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1398+4483T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47827866 | |||||||
| chr2:47828172 | A | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+4177T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828172 | |||||||
| chr2:47828216 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1398+4133A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828216 | |||||||
| chr2:47828344 | C | G | 10 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(7): Show |
10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1398+4005G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828344 | |||||||
| chr2:47828419 | C | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+3930G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828419 | |||||||
| chr2:47828468 | C | T | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+3881G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828468 | |||||||
| chr2:47828521 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1398+3828A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828521 | |||||||
| chr2:47828571 | T | C | 11 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0138 others(8): Show |
11 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398+3778A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828571 | |||||||
| chr2:47828603 | T | C | 5 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(2): Show |
5 | HG01074.hp2 HG01891.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398+3746A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828603 | |||||||
| chr2:47828609 | C | CA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0001g0101 others(3): Show |
6 | HG00544.hp2 HG02135.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1398+3739dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828609 | |||||||
| chr2:47828609 | CA | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+3739delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828609 | |||||||
| chr2:47828821 | T | C | 2 | a0001c0002t0002g0123 a0001c0002t0002g0298 |
2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1398+3528A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828821 | |||||||
| chr2:47828860 | CTTA | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0001g0091 others(3): Show |
6 | NA18971.hp2 NA19066.hp1 NA19074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1398+3486_1398+348 others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828860 | |||||||
| chr2:47828904 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1398+3445T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828904 | |||||||
| chr2:47828977 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1398+3372A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47828977 | |||||||
| chr2:47829029 | C | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+3320G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829029 | |||||||
| chr2:47829055 | G | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0223 |
3 | HG02809.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1398+3294C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829055 | |||||||
| chr2:47829092 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1398+3257C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829092 | |||||||
| chr2:47829110 | G | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+3239C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829110 | |||||||
| chr2:47829280 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1398+3069C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829280 | |||||||
| chr2:47829365 | C | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0177 |
2 | NA18998.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1398+2984G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829365 | |||||||
| chr2:47829834 | T | G | 6 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1398+2515A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829834 | |||||||
| chr2:47829905 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1398+2444A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829905 | |||||||
| chr2:47829968 | C | A | 1 | a0001c0001t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1398+2381G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47829968 | |||||||
| chr2:47830015 | A | G | 20 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(17): Show |
20 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1398+2334T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830015 | |||||||
| chr2:47830149 | T | A | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+2200A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830149 | |||||||
| chr2:47830181 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | NA18946.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1398+2168C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830181 | |||||||
| chr2:47830201 | A | G | 9 | a0001c0001t0003g0232 a0001c0002t0002g0196 a0001c0002t0002g0197 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+2148T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830201 | |||||||
| chr2:47830282 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1398+2067C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830282 | |||||||
| chr2:47830350 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1398+1999G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830350 | |||||||
| chr2:47830371 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1398+1978G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830371 | |||||||
| chr2:47830388 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0002g0234 |
2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1398+1961T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830388 | |||||||
| chr2:47830418 | G | C | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+1931C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830418 | |||||||
| chr2:47830515 | A | T | 1 | a0001c0001t0001g0066 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1398+1834T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830515 | |||||||
| chr2:47830581 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1398+1768A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830581 | |||||||
| chr2:47830597 | A | G | 1 | a0001c0002t0002g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1398+1752T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830597 | |||||||
| chr2:47830668 | T | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | NA18957.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1398+1681A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830668 | |||||||
| chr2:47830676 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1398+1673G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830676 | |||||||
| chr2:47830788 | G | C | 4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(1): Show |
4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1398+1561C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830788 | |||||||
| chr2:47830921 | C | T | 4 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0282 others(1): Show |
4 | HG02027.hp1 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398+1428G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830921 | |||||||
| chr2:47830948 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1398+1401C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47830948 | |||||||
| chr2:47831019 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1398+1330C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831019 | |||||||
| chr2:47831037 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1398+1312C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831037 | |||||||
| chr2:47831083 | G | A | 1 | a0001c0001t0002g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1398+1266C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831083 | |||||||
| chr2:47831094 | C | T | 26 | a0001c0001t0001g0040 a0001c0001t0001g0062 a0001c0001t0001g0128 others(23): Show |
26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1398+1255G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831094 | |||||||
| chr2:47831142 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
18 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1398+1207G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831142 | |||||||
| chr2:47831298 | C | T | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+1051G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831298 | |||||||
| chr2:47831427 | G | GA | 22 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0088 others(19): Show |
22 | HG00280.hp1 HG00544.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1398+921dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831427 | |||||||
| chr2:47831427 | GA | G | 10 | a0001c0001t0001g0047 a0001c0001t0001g0068 a0001c0001t0001g0111 others(7): Show |
10 | HG00280.hp2 HG00621.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1398+921delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831427 | |||||||
| chr2:47831427 | GAA | G | 21 | a0001c0001t0001g0109 a0001c0001t0001g0158 a0001c0001t0001g0159 others(18): Show |
21 | HG00621.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1398+920_1398+921d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831427 | |||||||
| chr2:47831452 | A | C | 25 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(22): Show |
25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1398+897T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831452 | |||||||
| chr2:47831503 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+846A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831503 | |||||||
| chr2:47831785 | A | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+564T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831785 | |||||||
| chr2:47831838 | A | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0223 |
3 | HG02809.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1398+511T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831838 | |||||||
| chr2:47831977 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1398+372T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831977 | |||||||
| chr2:47831990 | C | G | 1 | a0001c0001t0001g0004 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1398+359G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831990 | |||||||
| chr2:47831998 | TG | T | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1398+350delC | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47831998 | |||||||
| chr2:47832020 | T | C | 32 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(29): Show |
32 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1398+329A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832020 | |||||||
| chr2:47832098 | G | C | 1 | a0001c0001t0002g0247 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1398+251C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832098 | |||||||
| chr2:47832294 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1398+55A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832294 | |||||||
| chr2:47832330 | TAAA | T | 3 | a0001c0001t0001g0256 a0001c0001t0002g0095 a0001c0001t0002g0236 |
3 | NA19066.hp2 NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1398+16_1398+18del others(3): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832330 | |||||||
| chr2:47832332 | AAAAT | A | 43 | a0001c0001t0001g0164 a0001c0001t0001g0237 a0001c0001t0001g0286 others(40): Show |
43 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1398+13_1398+16del others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832332 | |||||||
| chr2:47832336 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1398+13A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 11/22 | chr2 | 47832336 | |||||||
| chr2:47832697 | T | G | 1 | a0001c0001t0002g0289 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1154-19A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 9/22 | chr2 | 47832697 | |||||||
| chr2:47833130 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.935-60A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833130 | |||||||
| chr2:47833174 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.935-104C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833174 | |||||||
| chr2:47833205 | C | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
18 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.935-135G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833205 | |||||||
| chr2:47833242 | T | C | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0223 others(1): Show |
4 | HG02809.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.935-172A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833242 | |||||||
| chr2:47833337 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.935-267C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833337 | |||||||
| chr2:47833418 | T | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0002g0163 |
3 | NA18962.hp2 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.935-348A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833418 | |||||||
| chr2:47833450 | A | C | 1 | a0001c0001t0002g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.935-380T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833450 | |||||||
| chr2:47833510 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.935-440C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833510 | |||||||
| chr2:47833641 | G | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.935-571C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833641 | |||||||
| chr2:47833737 | T | C | 14 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(11): Show |
14 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.935-667A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833737 | |||||||
| chr2:47833794 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.935-724G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833794 | |||||||
| chr2:47833808 | G | A | 10 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(7): Show |
10 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.935-738C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833808 | |||||||
| chr2:47833978 | T | G | 2 | a0001c0002t0002g0123 a0001c0002t0002g0298 |
2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.934+601A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47833978 | |||||||
| chr2:47834057 | G | C | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.934+522C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834057 | |||||||
| chr2:47834082 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+497C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834082 | |||||||
| chr2:47834171 | G | A | 1 | a0001c0001t0020g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934+408C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834171 | |||||||
| chr2:47834201 | T | C | 1 | a0004c0005t0002g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.934+378A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834201 | |||||||
| chr2:47834208 | C | G | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.934+371G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834208 | |||||||
| chr2:47834289 | A | G | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.934+290T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834289 | |||||||
| chr2:47834333 | T | C | 2 | a0001c0002t0002g0123 a0001c0002t0002g0298 |
2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.934+246A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834333 | |||||||
| chr2:47834395 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.934+184A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834395 | |||||||
| chr2:47834472 | CCAG | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.934+104_934+106del others(3): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 7/22 | chr2 | 47834472 | |||||||
| chr2:47835049 | C | G | 3 | a0001c0001t0001g0253 a0001c0001t0002g0005 a0001c0001t0016g0308 |
4 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-178G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835049 | |||||||
| chr2:47835098 | A | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-227T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835098 | |||||||
| chr2:47835207 | A | G | 5 | a0001c0001t0003g0135 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-336T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835207 | |||||||
| chr2:47835230 | A | T | 1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718-359T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835230 | |||||||
| chr2:47835232 | C | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-361G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835232 | |||||||
| chr2:47835363 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.718-492G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835363 | |||||||
| chr2:47835371 | T | C | 6 | a0001c0001t0001g0119 a0001c0001t0001g0273 a0001c0001t0001g0274 others(3): Show |
6 | HG01074.hp2 HG01891.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-500A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835371 | |||||||
| chr2:47835622 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+250C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835622 | |||||||
| chr2:47835644 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.717+228A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835644 | |||||||
| chr2:47835645 | G | A | 46 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0055 others(43): Show |
46 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.717+227C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835645 | |||||||
| chr2:47835749 | C | G | 5 | a0001c0001t0003g0135 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+123G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 5/22 | chr2 | 47835749 | |||||||
| chr2:47836027 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.588-26A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836027 | |||||||
| chr2:47836102 | G | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-101C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836102 | |||||||
| chr2:47836110 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0118 |
2 | NA18966.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.588-109C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836110 | |||||||
| chr2:47836110 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.588-109C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836110 | |||||||
| chr2:47836112 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0118 |
2 | NA18966.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.588-111T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836112 | |||||||
| chr2:47836176 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.588-175A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836176 | |||||||
| chr2:47836251 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.588-250C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836251 | |||||||
| chr2:47836516 | A | G | 1 | a0001c0001t0002g0288 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.588-515T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836516 | |||||||
| chr2:47836559 | A | G | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.588-558T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836559 | |||||||
| chr2:47836595 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.588-594G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836595 | |||||||
| chr2:47836652 | A | C | 1 | a0001c0001t0001g0286 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.588-651T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47836652 | |||||||
| chr2:47837075 | A | T | 1 | a0001c0001t0001g0286 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.588-1074T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837075 | |||||||
| chr2:47837176 | T | C | 2 | a0001c0002t0002g0123 a0001c0002t0002g0298 |
2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.588-1175A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837176 | |||||||
| chr2:47837238 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.588-1237T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837238 | |||||||
| chr2:47837502 | G | A | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.587+1357C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837502 | |||||||
| chr2:47837576 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.587+1283A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837576 | |||||||
| chr2:47837776 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.587+1083C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837776 | |||||||
| chr2:47837793 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0166 |
3 | HG01070.hp2 HG01071.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.587+1066G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837793 | |||||||
| chr2:47837871 | C | G | 1 | a0003c0004t0002g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.587+988G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837871 | |||||||
| chr2:47837904 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.587+955G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837904 | |||||||
| chr2:47837909 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+950A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837909 | |||||||
| chr2:47837992 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+867C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47837992 | |||||||
| chr2:47838061 | CA | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(213): Show |
221 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.587+797delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838061 | |||||||
| chr2:47838061 | CAA | C | 18 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(15): Show |
18 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.587+796_587+797del others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838061 | |||||||
| chr2:47838104 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0052 |
2 | HG02071.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.587+755T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838104 | |||||||
| chr2:47838428 | G | GAATTACT others(22): Show |
14 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0136 others(11): Show |
15 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.587+402_587+430dup others(29): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838428 | |||||||
| chr2:47838498 | G | T | 1 | a0001c0001t0002g0235 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.587+361C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838498 | |||||||
| chr2:47838605 | C | T | 29 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0207 others(26): Show |
29 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.587+254G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 4/22 | chr2 | 47838605 | |||||||
| chr2:47839092 | G | C | 5 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-89C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 3/22 | chr2 | 47839092 | |||||||
| chr2:47839093 | CT | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.443-91delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 3/22 | chr2 | 47839093 | |||||||
| chr2:47839130 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443-127A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 3/22 | chr2 | 47839130 | |||||||
| chr2:47839505 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18747.hp2 NA18946.hp2 |
splice_region_variant&intron_variant | LOW | c.361-5T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 2/22 | chr2 | 47839505 | |||||||
| chr2:47839607 | A | G | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.360+35T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 2/22 | chr2 | 47839607 | |||||||
| chr2:47839872 | G | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.233-103C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47839872 | |||||||
| chr2:47840029 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0088 a0001c0001t0001g0299 others(1): Show |
4 | HG02071.hp1 NA18967.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-260G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840029 | |||||||
| chr2:47840093 | G | A | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-324C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840093 | |||||||
| chr2:47840128 | A | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-359T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840128 | |||||||
| chr2:47840144 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.233-375G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840144 | |||||||
| chr2:47840164 | TG | T | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-396delC | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840164 | |||||||
| chr2:47840195 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.233-426C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840195 | |||||||
| chr2:47840273 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.233-504C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840273 | |||||||
| chr2:47840451 | CT | C | 14 | a0001c0001t0001g0162 a0001c0001t0001g0231 a0001c0001t0002g0234 others(11): Show |
14 | HG00735.hp1 HG01070.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.233-683delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840451 | |||||||
| chr2:47840487 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233-718C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840487 | |||||||
| chr2:47840490 | A | G | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-721T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840490 | |||||||
| chr2:47840513 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.233-744G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840513 | |||||||
| chr2:47840641 | A | G | 1 | a0001c0002t0002g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.233-872T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840641 | |||||||
| chr2:47840723 | C | T | 1 | a0001c0001t0009g0011 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.233-954G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840723 | |||||||
| chr2:47840726 | C | G | 1 | a0001c0001t0001g0192 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.233-957G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840726 | |||||||
| chr2:47840738 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.233-969C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840738 | |||||||
| chr2:47840853 | TA | T | 17 | a0001c0001t0001g0068 a0001c0001t0001g0128 a0001c0001t0001g0153 others(14): Show |
17 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.233-1085delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47840853 | |||||||
| chr2:47841142 | G | A | 2 | a0001c0001t0003g0232 a0004c0005t0002g0307 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.233-1373C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841142 | |||||||
| chr2:47841197 | C | CA | 7 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0160 others(4): Show |
7 | HG00642.hp2 HG01261.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.233-1429dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841197 | |||||||
| chr2:47841404 | C | G | 2 | a0001c0001t0001g0278 a0001c0001t0001g0280 |
2 | HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.233-1635G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841404 | |||||||
| chr2:47841488 | A | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0001g0186 others(2): Show |
5 | HG00544.hp1 NA18952.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-1719T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841488 | |||||||
| chr2:47841508 | C | T | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0207 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-1739G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841508 | |||||||
| chr2:47841846 | G | T | 1 | a0001c0001t0002g0259 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.233-2077C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841846 | |||||||
| chr2:47841919 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0273 a0001c0001t0001g0274 others(3): Show |
6 | HG01074.hp2 HG01891.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-2150C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841919 | |||||||
| chr2:47841974 | T | A | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-2205A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47841974 | |||||||
| chr2:47842021 | A | AT | 8 | a0001c0001t0001g0151 a0001c0001t0001g0225 a0001c0001t0001g0226 others(5): Show |
8 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-2253dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842021 | |||||||
| chr2:47842026 | T | TA | 5 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0300 others(2): Show |
5 | HG02257.hp2 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-2258_233-2257i others(3): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842026 | |||||||
| chr2:47842164 | C | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-2395G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842164 | |||||||
| chr2:47842306 | C | T | 20 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0207 others(17): Show |
20 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.233-2537G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842306 | |||||||
| chr2:47842374 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.233-2605A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842374 | |||||||
| chr2:47842399 | A | C | 4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(1): Show |
4 | HG01261.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-2630T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842399 | |||||||
| chr2:47842544 | T | G | 1 | a0001c0001t0001g0040 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.233-2775A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842544 | |||||||
| chr2:47842553 | C | T | 24 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(21): Show |
24 | HG01109.hp2 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.233-2784G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842553 | |||||||
| chr2:47842604 | T | TA | 9 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0210 others(6): Show |
10 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-2836dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842604 | |||||||
| chr2:47842779 | TA | T | 71 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(68): Show |
71 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.233-3011delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842779 | |||||||
| chr2:47842881 | A | G | 4 | a0001c0001t0003g0121 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-3112T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842881 | |||||||
| chr2:47842905 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.233-3136G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47842905 | |||||||
| chr2:47843136 | G | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0250 |
2 | NA18993.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.233-3367C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843136 | |||||||
| chr2:47843160 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(13): Show |
17 | HG03492.hp2 HG03704.hp1 NA18942.hp2 others(14): Show |
intron_variant | MODIFIER | c.233-3391A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843160 | |||||||
| chr2:47843431 | CT | C | 21 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(18): Show |
21 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.233-3663delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843431 | |||||||
| chr2:47843517 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0210 a0001c0001t0001g0212 others(5): Show |
9 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.233-3748A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843517 | |||||||
| chr2:47843615 | C | G | 5 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(2): Show |
5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-3846G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843615 | |||||||
| chr2:47843678 | T | A | 14 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(11): Show |
14 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.233-3909A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843678 | |||||||
| chr2:47843728 | G | GCTT | 14 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(11): Show |
14 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.233-3960_233-3959i others(5): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843728 | |||||||
| chr2:47843728 | G | GCTTCTTC others(2): Show |
3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
3 | HG00738.hp1 HG02559.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.233-3960_233-3959i others(11): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843728 | |||||||
| chr2:47843728 | G | GCTTCTTC others(5): Show |
1 | a0001c0001t0014g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233-3960_233-3959i others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843728 | |||||||
| chr2:47843731 | G | T | 21 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(18): Show |
21 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.233-3962C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843731 | |||||||
| chr2:47843734 | G | T | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-3965C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843734 | |||||||
| chr2:47843737 | T | G | 13 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0164 others(10): Show |
13 | HG00099.hp1 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.233-3968A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843737 | |||||||
| chr2:47843865 | C | A | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-4096G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843865 | |||||||
| chr2:47843898 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.233-4129C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843898 | |||||||
| chr2:47843902 | G | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-4133C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47843902 | |||||||
| chr2:47844116 | T | A | 25 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(22): Show |
25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.233-4347A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844116 | |||||||
| chr2:47844183 | A | C | 1 | a0001c0002t0002g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.233-4414T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844183 | |||||||
| chr2:47844379 | T | A | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | NA18747.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.233-4610A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844379 | |||||||
| chr2:47844431 | C | T | 2 | a0003c0004t0002g0195 a0003c0004t0002g0203 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.233-4662G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844431 | |||||||
| chr2:47844511 | GCTATA | G | 14 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(11): Show |
14 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.233-4747_233-4743d others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844511 | |||||||
| chr2:47844517 | T | A | 14 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(11): Show |
14 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.233-4748A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844517 | |||||||
| chr2:47844636 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.233-4867A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844636 | |||||||
| chr2:47844720 | C | T | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-4951G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844720 | |||||||
| chr2:47844957 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.233-5188C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47844957 | |||||||
| chr2:47845007 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.233-5238A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845007 | |||||||
| chr2:47845019 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.233-5250A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845019 | |||||||
| chr2:47845052 | G | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0250 |
2 | NA18993.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.233-5283C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845052 | |||||||
| chr2:47845152 | C | G | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-5383G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845152 | |||||||
| chr2:47845164 | T | A | 6 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-5395A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845164 | |||||||
| chr2:47845498 | G | A | 1 | a0004c0005t0002g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.233-5729C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845498 | |||||||
| chr2:47845716 | G | A | 53 | a0001c0001t0001g0036 a0001c0001t0001g0237 a0001c0001t0001g0253 others(50): Show |
54 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.233-5947C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845716 | |||||||
| chr2:47845872 | A | C | 11 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(8): Show |
11 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-6103T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845872 | |||||||
| chr2:47845888 | G | GAA | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-6121_233-6120d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845888 | |||||||
| chr2:47845978 | C | T | 25 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(22): Show |
25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.233-6209G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47845978 | |||||||
| chr2:47846220 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.233-6451G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846220 | |||||||
| chr2:47846297 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.233-6528C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846297 | |||||||
| chr2:47846401 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.233-6632G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846401 | |||||||
| chr2:47846529 | T | A | 8 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
8 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-6760A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846529 | |||||||
| chr2:47846532 | T | C | 4 | a0001c0001t0002g0261 a0003c0004t0002g0195 a0003c0004t0002g0203 others(1): Show |
4 | HG01884.hp1 HG02896.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-6763A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846532 | |||||||
| chr2:47846583 | A | AAT | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-6816_233-6815d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846583 | |||||||
| chr2:47846602 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.233-6833T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846602 | |||||||
| chr2:47846610 | T | G | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.233-6841A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846610 | |||||||
| chr2:47846676 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-6907A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846676 | |||||||
| chr2:47846738 | TATATC | T | 15 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(12): Show |
15 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6974_233-6970d others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846738 | |||||||
| chr2:47846834 | C | T | 3 | a0003c0004t0002g0195 a0003c0004t0002g0203 a0003c0004t0002g0204 |
3 | HG01884.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.233-7065G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846834 | |||||||
| chr2:47846855 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.233-7086G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47846855 | |||||||
| chr2:47847194 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-7425C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847194 | |||||||
| chr2:47847275 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.233-7506A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847275 | |||||||
| chr2:47847332 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.233-7563A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847332 | |||||||
| chr2:47847422 | A | G | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-7653T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847422 | |||||||
| chr2:47847444 | C | A | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-7675G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847444 | |||||||
| chr2:47847450 | T | C | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-7681A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847450 | |||||||
| chr2:47847981 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.233-8212C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47847981 | |||||||
| chr2:47848127 | A | C | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-8358T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848127 | |||||||
| chr2:47848142 | AC | A | 13 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(10): Show |
13 | HG00738.hp1 HG01346.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.233-8374delG | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848142 | |||||||
| chr2:47848143 | C | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.233-8374G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848143 | |||||||
| chr2:47848143 | CA | C | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-8375delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848143 | |||||||
| chr2:47848157 | A | AAC | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-8390_233-8389d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848157 | |||||||
| chr2:47848212 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.233-8443C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848212 | |||||||
| chr2:47848263 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-8494A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848263 | |||||||
| chr2:47848301 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.233-8532G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848301 | |||||||
| chr2:47848312 | G | C | 7 | a0001c0001t0002g0056 a0001c0001t0002g0249 a0001c0001t0002g0263 others(4): Show |
7 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-8543C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848312 | |||||||
| chr2:47848789 | A | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG00621.hp1 HG01993.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.233-9020T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848789 | |||||||
| chr2:47848792 | A | G | 2 | a0001c0001t0003g0232 a0004c0005t0002g0307 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.233-9023T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848792 | |||||||
| chr2:47848827 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.233-9058G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848827 | |||||||
| chr2:47848910 | A | ACACATTT others(5): Show |
1 | a0001c0001t0001g0299 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.233-9153_233-9142d others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848910 | |||||||
| chr2:47848963 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.233-9194C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848963 | |||||||
| chr2:47848993 | A | G | 4 | a0001c0001t0003g0121 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-9224T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47848993 | |||||||
| chr2:47849002 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233-9233G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849002 | |||||||
| chr2:47849060 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.233-9291C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849060 | |||||||
| chr2:47849149 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-9380A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849149 | |||||||
| chr2:47849156 | T | TA | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.233-9388dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849156 | |||||||
| chr2:47849180 | A | G | 6 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-9411T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849180 | |||||||
| chr2:47849243 | G | A | 7 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0001g0091 others(4): Show |
7 | NA18971.hp2 NA19010.hp2 NA19066.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-9474C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849243 | |||||||
| chr2:47849409 | A | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG01255.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.233-9640T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849409 | |||||||
| chr2:47849940 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-10171C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849940 | |||||||
| chr2:47849950 | G | T | 72 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(69): Show |
73 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.233-10181C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47849950 | |||||||
| chr2:47850040 | G | C | 13 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(10): Show |
13 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.233-10271C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850040 | |||||||
| chr2:47850153 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0012g0175 a0001c0001t0019g0311 |
3 | NA18952.hp2 NA18965.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.233-10384C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850153 | |||||||
| chr2:47850253 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.233-10484C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850253 | |||||||
| chr2:47850360 | A | C | 6 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0208 others(3): Show |
6 | HG02717.hp2 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-10591T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850360 | |||||||
| chr2:47850449 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.233-10680C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850449 | |||||||
| chr2:47850515 | C | T | 6 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0073 others(3): Show |
6 | HG00609.hp2 HG02080.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-10746G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850515 | |||||||
| chr2:47850566 | A | T | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-10797T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850566 | |||||||
| chr2:47850653 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.233-10884T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850653 | |||||||
| chr2:47850702 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.233-10933T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850702 | |||||||
| chr2:47850895 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0002g0124 a0001c0001t0002g0125 others(2): Show |
5 | HG00738.hp1 HG02056.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-11126T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850895 | |||||||
| chr2:47850919 | G | A | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-11150C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47850919 | |||||||
| chr2:47851053 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.233-11284C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851053 | |||||||
| chr2:47851072 | A | T | 15 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(12): Show |
15 | HG01346.hp1 HG02615.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-11303T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851072 | |||||||
| chr2:47851154 | A | AAATTAAC | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.233-11386_233-1138 others(11): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851154 | |||||||
| chr2:47851188 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-11419C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851188 | |||||||
| chr2:47851198 | C | T | 9 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(6): Show |
9 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.233-11429G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851198 | |||||||
| chr2:47851330 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.233-11561C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851330 | |||||||
| chr2:47851454 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.233-11685G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851454 | |||||||
| chr2:47851542 | G | C | 2 | a0001c0001t0002g0249 a0001c0001t0002g0263 |
2 | HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.233-11773C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851542 | |||||||
| chr2:47851699 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.233-11930G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851699 | |||||||
| chr2:47851874 | T | G | 8 | a0001c0001t0001g0122 a0001c0001t0001g0210 a0001c0001t0001g0212 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-12105A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851874 | |||||||
| chr2:47851968 | A | C | 1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233-12199T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851968 | |||||||
| chr2:47851989 | A | AT | 18 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(15): Show |
18 | HG00544.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-12221dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851989 | |||||||
| chr2:47851989 | A | ATTT | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-12223_233-1222 others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851989 | |||||||
| chr2:47851989 | AT | A | 23 | a0001c0001t0001g0065 a0001c0001t0001g0093 a0001c0001t0001g0115 others(20): Show |
23 | HG00099.hp2 HG01099.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.233-12221delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47851989 | |||||||
| chr2:47852017 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.233-12248T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852017 | |||||||
| chr2:47852062 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.233-12293C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852062 | |||||||
| chr2:47852157 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.233-12388A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852157 | |||||||
| chr2:47852187 | G | A | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233-12418C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852187 | |||||||
| chr2:47852318 | C | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | HG02135.hp1 NA18977.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-12549G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852318 | |||||||
| chr2:47852347 | A | C | 1 | a0001c0001t0002g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.233-12578T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852347 | |||||||
| chr2:47852347 | A | G | 10 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(7): Show |
10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-12578T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852347 | |||||||
| chr2:47852448 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.233-12679T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852448 | |||||||
| chr2:47852549 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.233-12780G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852549 | |||||||
| chr2:47852564 | G | C | 7 | a0001c0001t0002g0056 a0001c0001t0002g0249 a0001c0001t0002g0263 others(4): Show |
7 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-12795C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852564 | |||||||
| chr2:47852710 | A | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0223 |
3 | HG02809.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233-12941T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852710 | |||||||
| chr2:47852839 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-13070A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852839 | |||||||
| chr2:47852941 | C | A | 1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233-13172G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852941 | |||||||
| chr2:47852963 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0118 |
2 | NA18966.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.233-13194T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47852963 | |||||||
| chr2:47853075 | A | AT | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(13): Show |
16 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.233-13307dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853075 | |||||||
| chr2:47853121 | C | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.233-13352G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853121 | |||||||
| chr2:47853416 | T | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0250 |
2 | NA18993.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.233-13647A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853416 | |||||||
| chr2:47853424 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.233-13655A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853424 | |||||||
| chr2:47853426 | T | C | 1 | a0005c0006t0001g0051 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.233-13657A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853426 | |||||||
| chr2:47853454 | C | G | 1 | a0001c0001t0001g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.233-13685G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853454 | |||||||
| chr2:47853506 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-13737C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853506 | |||||||
| chr2:47853533 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.233-13764G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853533 | |||||||
| chr2:47853687 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.233-13918G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853687 | |||||||
| chr2:47853762 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-13993A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853762 | |||||||
| chr2:47853836 | G | A | 2 | a0001c0002t0002g0196 a0001c0002t0002g0298 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.233-14067C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853836 | |||||||
| chr2:47853881 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.233-14112T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853881 | |||||||
| chr2:47853921 | A | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-14152T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853921 | |||||||
| chr2:47853927 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.233-14158C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47853927 | |||||||
| chr2:47854256 | CT | C | 7 | a0001c0001t0001g0134 a0001c0001t0001g0143 a0001c0001t0001g0237 others(4): Show |
7 | HG00738.hp1 HG01069.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-14488delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854256 | |||||||
| chr2:47854343 | T | TA | 3 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0052 |
3 | HG00621.hp1 HG02071.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.233-14575dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854343 | |||||||
| chr2:47854357 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.233-14588G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854357 | |||||||
| chr2:47854368 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0157 |
2 | HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.233-14599G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854368 | |||||||
| chr2:47854620 | C | T | 1 | a0001c0001t0018g0310 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.233-14851G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854620 | |||||||
| chr2:47854660 | T | C | 1 | a0004c0005t0002g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.233-14891A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854660 | |||||||
| chr2:47854863 | G | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0207 a0001c0001t0002g0124 others(7): Show |
10 | HG00738.hp1 HG02300.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-15094C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854863 | |||||||
| chr2:47854863 | GT | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(264): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.233-15095delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854863 | |||||||
| chr2:47854864 | T | G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0207 a0001c0001t0002g0124 others(7): Show |
10 | HG00738.hp1 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-15095A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47854864 | |||||||
| chr2:47855052 | G | T | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-15283C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855052 | |||||||
| chr2:47855057 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233-15288A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855057 | |||||||
| chr2:47855073 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.233-15304A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855073 | |||||||
| chr2:47855097 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.233-15328T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855097 | |||||||
| chr2:47855200 | A | AT | 12 | a0001c0001t0002g0236 a0001c0001t0003g0121 a0001c0002t0002g0123 others(9): Show |
12 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.233-15432dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855200 | |||||||
| chr2:47855201 | T | A | 1 | a0001c0001t0001g0237 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.233-15432A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855201 | |||||||
| chr2:47855227 | G | T | 1 | a0001c0001t0002g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.233-15458C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855227 | |||||||
| chr2:47855259 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.233-15490C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855259 | |||||||
| chr2:47855261 | C | A | 1 | a0001c0001t0002g0033 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.233-15492G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855261 | |||||||
| chr2:47855285 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-15516G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855285 | |||||||
| chr2:47855476 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.233-15707C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855476 | |||||||
| chr2:47855508 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01891.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.233-15739C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855508 | |||||||
| chr2:47855609 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.233-15840A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855609 | |||||||
| chr2:47855613 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.233-15844G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855613 | |||||||
| chr2:47855758 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.233-15989C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855758 | |||||||
| chr2:47855836 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.233-16067G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855836 | |||||||
| chr2:47855841 | C | CA | 21 | a0001c0001t0001g0083 a0001c0001t0001g0106 a0001c0001t0001g0158 others(18): Show |
21 | HG00280.hp2 HG00597.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.233-16073dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855841 | |||||||
| chr2:47855841 | CA | C | 6 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
6 | HG00621.hp1 HG02071.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-16073delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855841 | |||||||
| chr2:47855864 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.233-16095G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855864 | |||||||
| chr2:47855890 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-16121C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47855890 | |||||||
| chr2:47856433 | G | T | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.233-16664C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47856433 | |||||||
| chr2:47856472 | A | C | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233-16703T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47856472 | |||||||
| chr2:47856639 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.233-16870C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47856639 | |||||||
| chr2:47856785 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.233-17016T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47856785 | |||||||
| chr2:47857267 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0069 |
2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.233-17498A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857267 | |||||||
| chr2:47857282 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0210 a0001c0001t0001g0212 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-17513C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857282 | |||||||
| chr2:47857423 | A | T | 27 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(24): Show |
27 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.233-17654T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857423 | |||||||
| chr2:47857519 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.233-17750G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857519 | |||||||
| chr2:47857533 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0030 |
3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.233-17764G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857533 | |||||||
| chr2:47857808 | T | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
4 | NA18957.hp2 NA19012.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-18039A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857808 | |||||||
| chr2:47857922 | C | A | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(190): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.233-18153G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857922 | |||||||
| chr2:47857948 | T | TAC | 49 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0037 others(46): Show |
50 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.233-18181_233-1818 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47857948 | |||||||
| chr2:47858022 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.233-18253C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858022 | |||||||
| chr2:47858071 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.233-18302C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858071 | |||||||
| chr2:47858261 | C | T | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-18492G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858261 | |||||||
| chr2:47858397 | A | T | 1 | a0002c0003t0001g0013 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.233-18628T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858397 | |||||||
| chr2:47858422 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.233-18653G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858422 | |||||||
| chr2:47858525 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-18756A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858525 | |||||||
| chr2:47858566 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0052 |
3 | HG00621.hp1 HG02071.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.233-18797G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858566 | |||||||
| chr2:47858577 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.233-18808C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858577 | |||||||
| chr2:47858675 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.233-18906G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858675 | |||||||
| chr2:47858681 | C | CA | 35 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(32): Show |
36 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.233-18913dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858681 | |||||||
| chr2:47858681 | CA | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0128 others(74): Show |
78 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.233-18913delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858681 | |||||||
| chr2:47858696 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.233-18927T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858696 | |||||||
| chr2:47858771 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.233-19002C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47858771 | |||||||
| chr2:47859041 | CA | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(259): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.233-19273delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859041 | |||||||
| chr2:47859041 | CAA | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.233-19274_233-1927 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859041 | |||||||
| chr2:47859124 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.233-19355A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859124 | |||||||
| chr2:47859197 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.233-19428A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859197 | |||||||
| chr2:47859379 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233-19610C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859379 | |||||||
| chr2:47859543 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.233-19774G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859543 | |||||||
| chr2:47859656 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233-19887G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859656 | |||||||
| chr2:47859684 | C | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG00621.hp1 HG01993.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.233-19915G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859684 | |||||||
| chr2:47859715 | T | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-19946A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859715 | |||||||
| chr2:47859737 | T | G | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.233-19968A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859737 | |||||||
| chr2:47859868 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.233-20099C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859868 | |||||||
| chr2:47859888 | C | G | 26 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(23): Show |
26 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.233-20119G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47859888 | |||||||
| chr2:47860192 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.233-20423C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860192 | |||||||
| chr2:47860320 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.233-20551C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860320 | |||||||
| chr2:47860400 | T | C | 2 | a0001c0001t0003g0121 a0001c0001t0003g0232 |
2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.233-20631A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860400 | |||||||
| chr2:47860410 | A | AT | 18 | a0001c0001t0001g0049 a0001c0001t0001g0075 a0001c0001t0001g0105 others(15): Show |
18 | HG01993.hp1 HG02145.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-20642dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860410 | |||||||
| chr2:47860410 | AT | A | 10 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0001g0225 others(7): Show |
10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-20642delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860410 | |||||||
| chr2:47860543 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.233-20774A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860543 | |||||||
| chr2:47860657 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233-20888A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860657 | |||||||
| chr2:47860658 | C | T | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.233-20889G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860658 | |||||||
| chr2:47860687 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.233-20918C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860687 | |||||||
| chr2:47860691 | G | C | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.233-20922C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860691 | |||||||
| chr2:47860814 | GA | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.233-21046delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860814 | |||||||
| chr2:47860843 | AT | A | 169 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(166): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.233-21075delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860843 | |||||||
| chr2:47860843 | ATT | A | 8 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-21076_233-2107 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860843 | |||||||
| chr2:47860949 | T | C | 8 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-21180A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47860949 | |||||||
| chr2:47861009 | T | C | 29 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(26): Show |
29 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.233-21240A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861009 | |||||||
| chr2:47861099 | C | A | 2 | a0001c0001t0002g0124 a0001c0002t0002g0123 |
2 | HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.233-21330G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861099 | |||||||
| chr2:47861273 | A | G | 11 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(8): Show |
11 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-21504T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861273 | |||||||
| chr2:47861294 | T | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-21525A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861294 | |||||||
| chr2:47861318 | C | CT | 8 | a0001c0001t0001g0106 a0001c0001t0001g0225 a0001c0001t0001g0226 others(5): Show |
8 | HG00280.hp2 HG01081.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-21550dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861318 | |||||||
| chr2:47861356 | T | C | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0223 others(1): Show |
4 | HG02809.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-21587A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861356 | |||||||
| chr2:47861492 | A | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-21723T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861492 | |||||||
| chr2:47861495 | T | A | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0101 others(7): Show |
10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-21726A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861495 | |||||||
| chr2:47861610 | C | T | 1 | a0001c0002t0002g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233-21841G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861610 | |||||||
| chr2:47861677 | T | C | 1 | a0001c0002t0002g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.233-21908A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861677 | |||||||
| chr2:47861700 | T | A | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-21931A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861700 | |||||||
| chr2:47861717 | G | C | 6 | a0001c0001t0001g0119 a0001c0001t0001g0273 a0001c0001t0001g0274 others(3): Show |
6 | HG01074.hp2 HG01891.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-21948C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861717 | |||||||
| chr2:47861725 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.233-21956G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861725 | |||||||
| chr2:47861800 | G | C | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.233-22031C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861800 | |||||||
| chr2:47861907 | G | GT | 12 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0076 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.233-22139dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861907 | |||||||
| chr2:47861907 | GT | G | 12 | a0001c0001t0001g0024 a0001c0001t0001g0158 a0001c0001t0001g0159 others(9): Show |
12 | HG01169.hp2 HG01346.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.233-22139delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47861907 | |||||||
| chr2:47862065 | A | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-22296T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862065 | |||||||
| chr2:47862307 | A | C | 1 | a0001c0001t0002g0263 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.233-22538T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862307 | |||||||
| chr2:47862549 | A | C | 1 | a0001c0001t0002g0267 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.233-22780T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862549 | |||||||
| chr2:47862589 | G | C | 1 | a0001c0001t0001g0290 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.233-22820C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862589 | |||||||
| chr2:47862985 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.233-23216C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47862985 | |||||||
| chr2:47863055 | C | CA | 11 | a0001c0001t0001g0144 a0001c0001t0001g0185 a0001c0001t0001g0256 others(8): Show |
11 | HG01169.hp2 HG01175.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.233-23287dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863055 | |||||||
| chr2:47863055 | CA | C | 20 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(17): Show |
20 | HG00738.hp1 HG01109.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.233-23287delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863055 | |||||||
| chr2:47863064 | A | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23295T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863064 | |||||||
| chr2:47863065 | AAAAAAAC | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23303_233-2329 others(11): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863065 | |||||||
| chr2:47863071 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233-23303_233-2330 others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863071 | |||||||
| chr2:47863072 | C | A | 7 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0281 others(4): Show |
7 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23303G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863072 | |||||||
| chr2:47863086 | C | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23317G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863086 | |||||||
| chr2:47863178 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233-23409G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863178 | |||||||
| chr2:47863244 | T | C | 2 | a0001c0001t0004g0001 a0001c0001t0004g0012 |
3 | HG02135.hp2 HG02523.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.233-23475A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863244 | |||||||
| chr2:47863273 | A | G | 2 | a0001c0001t0001g0290 a0001c0001t0002g0289 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.233-23504T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863273 | |||||||
| chr2:47863346 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.233-23577T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863346 | |||||||
| chr2:47863404 | ACAT | A | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23638_233-2363 others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863404 | |||||||
| chr2:47863408 | G | A | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23639C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863408 | |||||||
| chr2:47863410 | C | A | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23641G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863410 | |||||||
| chr2:47863411 | T | G | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-23642A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863411 | |||||||
| chr2:47863440 | A | C | 1 | a0001c0001t0001g0296 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.233-23671T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863440 | |||||||
| chr2:47863694 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.233-23925T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863694 | |||||||
| chr2:47863832 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.233-24063A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863832 | |||||||
| chr2:47863870 | G | C | 2 | a0001c0001t0003g0232 a0004c0005t0002g0307 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.233-24101C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863870 | |||||||
| chr2:47863954 | C | T | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-24185G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47863954 | |||||||
| chr2:47864266 | G | C | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-24497C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864266 | |||||||
| chr2:47864269 | A | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(97): Show |
102 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.233-24500T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864269 | |||||||
| chr2:47864302 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.233-24533T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864302 | |||||||
| chr2:47864326 | G | A | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-24557C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864326 | |||||||
| chr2:47864327 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.233-24558G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864327 | |||||||
| chr2:47864584 | T | A | 29 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(26): Show |
29 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.233-24815A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864584 | |||||||
| chr2:47864588 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.233-24819T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864588 | |||||||
| chr2:47864769 | T | C | 2 | a0001c0002t0002g0201 a0001c0002t0002g0202 |
2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.233-25000A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864769 | |||||||
| chr2:47864820 | T | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0069 |
2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.233-25051A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47864820 | |||||||
| chr2:47865215 | T | G | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.233-25446A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865215 | |||||||
| chr2:47865291 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.233-25522A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865291 | |||||||
| chr2:47865487 | C | T | 3 | a0001c0001t0003g0232 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.233-25718G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865487 | |||||||
| chr2:47865526 | C | T | 11 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(8): Show |
11 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-25757G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865526 | |||||||
| chr2:47865686 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.233-25917A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865686 | |||||||
| chr2:47865702 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01891.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.233-25933A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865702 | |||||||
| chr2:47865750 | G | C | 1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233-25981C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865750 | |||||||
| chr2:47865799 | T | C | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233-26030A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865799 | |||||||
| chr2:47865823 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.233-26054A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47865823 | |||||||
| chr2:47866017 | G | T | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-26248C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866017 | |||||||
| chr2:47866139 | G | A | 1 | a0001c0001t0014g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233-26370C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866139 | |||||||
| chr2:47866245 | C | CA | 63 | a0001c0001t0001g0030 a0001c0001t0001g0043 a0001c0001t0001g0057 others(60): Show |
63 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.233-26477dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866245 | |||||||
| chr2:47866245 | CA | C | 27 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
27 | HG01069.hp2 HG01346.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.233-26477delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866245 | |||||||
| chr2:47866333 | C | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-26564G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866333 | |||||||
| chr2:47866337 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.233-26568G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866337 | |||||||
| chr2:47866365 | C | T | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-26596G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866365 | |||||||
| chr2:47866425 | G | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-26656C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866425 | |||||||
| chr2:47866440 | G | A | 8 | a0001c0002t0002g0196 a0001c0002t0002g0197 a0001c0002t0002g0198 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-26671C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866440 | |||||||
| chr2:47866497 | C | T | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-26728G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866497 | |||||||
| chr2:47866551 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.233-26782C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866551 | |||||||
| chr2:47866577 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0010g0217 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.233-26808C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866577 | |||||||
| chr2:47866614 | C | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-26845G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47866614 | |||||||
| chr2:47867058 | T | C | 1 | a0004c0005t0002g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.233-27289A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867058 | |||||||
| chr2:47867141 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.233-27372T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867141 | |||||||
| chr2:47867198 | G | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.233-27429C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867198 | |||||||
| chr2:47867426 | A | C | 1 | a0001c0001t0001g0294 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.233-27657T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867426 | |||||||
| chr2:47867622 | T | C | 1 | a0001c0001t0014g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233-27853A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867622 | |||||||
| chr2:47867722 | TAAGTCA | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-27959_233-2795 others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867722 | |||||||
| chr2:47867746 | A | G | 1 | a0003c0004t0002g0204 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.233-27977T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867746 | |||||||
| chr2:47867748 | T | C | 1 | a0001c0001t0002g0095 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.233-27979A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867748 | |||||||
| chr2:47867910 | T | A | 5 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(2): Show |
5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-28141A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867910 | |||||||
| chr2:47867926 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-28157A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867926 | |||||||
| chr2:47867927 | T | A | 3 | a0001c0001t0001g0176 a0001c0001t0012g0175 a0001c0001t0019g0311 |
3 | NA18952.hp2 NA18965.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.233-28158A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867927 | |||||||
| chr2:47867971 | A | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0158 others(21): Show |
25 | HG00738.hp1 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.233-28202T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47867971 | |||||||
| chr2:47868036 | G | A | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-28267C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868036 | |||||||
| chr2:47868178 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.233-28409C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868178 | |||||||
| chr2:47868200 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.233-28431A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868200 | |||||||
| chr2:47868208 | G | A | 1 | a0001c0001t0016g0308 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.233-28439C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868208 | |||||||
| chr2:47868282 | C | CA | 60 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0030 others(57): Show |
62 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.233-28514dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868282 | |||||||
| chr2:47868282 | CAA | C | 18 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(15): Show |
18 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.233-28515_233-2851 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868282 | |||||||
| chr2:47868436 | C | T | 36 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(33): Show |
36 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.233-28667G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868436 | |||||||
| chr2:47868507 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.233-28738T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868507 | |||||||
| chr2:47868594 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.233-28825A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868594 | |||||||
| chr2:47868715 | C | A | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-28946G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868715 | |||||||
| chr2:47868730 | C | G | 1 | a0001c0001t0020g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.233-28961G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868730 | |||||||
| chr2:47868748 | G | A | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-28979C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868748 | |||||||
| chr2:47868827 | G | A | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0193 others(1): Show |
4 | NA18971.hp1 NA18993.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-29058C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868827 | |||||||
| chr2:47868833 | G | A | 10 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
10 | HG03669.hp1 HG04184.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-29064C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868833 | |||||||
| chr2:47868891 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.233-29122A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47868891 | |||||||
| chr2:47869240 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233-29471G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869240 | |||||||
| chr2:47869384 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.233-29615A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869384 | |||||||
| chr2:47869386 | G | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-29617C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869386 | |||||||
| chr2:47869721 | G | T | 3 | a0001c0002t0002g0123 a0001c0002t0002g0196 a0001c0002t0002g0298 |
3 | HG01109.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.233-29952C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869721 | |||||||
| chr2:47869805 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.233-30036A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47869805 | |||||||
| chr2:47870027 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.233-30258C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870027 | |||||||
| chr2:47870284 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.233-30515G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870284 | |||||||
| chr2:47870318 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-30549A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870318 | |||||||
| chr2:47870406 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-30637A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870406 | |||||||
| chr2:47870578 | C | T | 6 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-30809G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870578 | |||||||
| chr2:47870650 | T | G | 1 | a0001c0001t0001g0286 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.233-30881A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870650 | |||||||
| chr2:47870688 | G | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-30919C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47870688 | |||||||
| chr2:47871000 | T | A | 6 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-31231A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871000 | |||||||
| chr2:47871038 | T | C | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.233-31269A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871038 | |||||||
| chr2:47871140 | A | G | 7 | a0001c0001t0002g0056 a0001c0001t0002g0249 a0001c0001t0002g0263 others(4): Show |
7 | HG02027.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-31371T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871140 | |||||||
| chr2:47871144 | T | G | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-31375A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871144 | |||||||
| chr2:47871185 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.233-31416C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871185 | |||||||
| chr2:47871230 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233-31461C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871230 | |||||||
| chr2:47871434 | T | C | 1 | a0001c0001t0009g0011 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.233-31665A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871434 | |||||||
| chr2:47871484 | T | C | 6 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-31715A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871484 | |||||||
| chr2:47871505 | T | C | 6 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-31736A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871505 | |||||||
| chr2:47871513 | C | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-31744G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871513 | |||||||
| chr2:47871569 | C | T | 48 | a0001c0001t0001g0237 a0001c0001t0001g0253 a0001c0001t0001g0271 others(45): Show |
49 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.233-31800G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871569 | |||||||
| chr2:47871657 | A | G | 3 | a0001c0001t0001g0253 a0001c0001t0002g0251 a0001c0001t0002g0252 |
3 | HG01168.hp1 HG01168.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.233-31888T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871657 | |||||||
| chr2:47871824 | C | T | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233-32055G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871824 | |||||||
| chr2:47871923 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.233-32154A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871923 | |||||||
| chr2:47871962 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-32193A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47871962 | |||||||
| chr2:47872359 | C | T | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-32590G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872359 | |||||||
| chr2:47872487 | C | T | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233-32718G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872487 | |||||||
| chr2:47872576 | G | A | 1 | a0001c0002t0002g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.233-32807C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872576 | |||||||
| chr2:47872666 | G | T | 1 | a0001c0001t0001g0290 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.232+32823C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872666 | |||||||
| chr2:47872917 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.232+32572A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47872917 | |||||||
| chr2:47873002 | T | C | 6 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+32487A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873002 | |||||||
| chr2:47873040 | T | G | 1 | a0001c0001t0002g0046 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.232+32449A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873040 | |||||||
| chr2:47873067 | A | C | 1 | a0001c0001t0011g0107 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.232+32422T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873067 | |||||||
| chr2:47873278 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.232+32211A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873278 | |||||||
| chr2:47873776 | A | G | 40 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(37): Show |
40 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.232+31713T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873776 | |||||||
| chr2:47873915 | T | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0282 others(1): Show |
4 | HG02809.hp2 HG03471.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+31574A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873915 | |||||||
| chr2:47873916 | A | T | 2 | a0001c0001t0001g0274 a0001c0001t0003g0232 |
2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.232+31573T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47873916 | |||||||
| chr2:47874030 | T | C | 1 | a0001c0001t0002g0265 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.232+31459A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874030 | |||||||
| chr2:47874150 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.232+31339G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874150 | |||||||
| chr2:47874160 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.232+31329C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874160 | |||||||
| chr2:47874161 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.232+31328G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874161 | |||||||
| chr2:47874221 | TAATA | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0002g0163 |
3 | NA18962.hp2 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.232+31264_232+3126 others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874221 | |||||||
| chr2:47874489 | C | G | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+31000G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874489 | |||||||
| chr2:47874534 | T | A | 1 | a0001c0001t0001g0002 | 2 | NA18942.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.232+30955A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874534 | |||||||
| chr2:47874542 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.232+30947T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874542 | |||||||
| chr2:47874669 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.232+30820C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874669 | |||||||
| chr2:47874681 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.232+30808A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874681 | |||||||
| chr2:47874771 | G | T | 4 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+30718C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874771 | |||||||
| chr2:47874773 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.232+30716C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874773 | |||||||
| chr2:47874867 | C | CT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(98): Show |
103 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.232+30621dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874867 | |||||||
| chr2:47874867 | C | CTT | 32 | a0001c0001t0001g0104 a0001c0001t0001g0136 a0001c0001t0001g0155 others(29): Show |
32 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.232+30620_232+3062 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874867 | |||||||
| chr2:47874867 | CT | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0279 a0001c0001t0001g0297 others(4): Show |
8 | HG00323.hp2 HG01069.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.232+30621delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874867 | |||||||
| chr2:47874887 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232+30602A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47874887 | |||||||
| chr2:47875025 | T | C | 41 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(38): Show |
41 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.232+30464A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875025 | |||||||
| chr2:47875042 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.232+30447T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875042 | |||||||
| chr2:47875091 | T | C | 5 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+30398A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875091 | |||||||
| chr2:47875092 | G | A | 26 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(23): Show |
26 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.232+30397C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875092 | |||||||
| chr2:47875139 | G | A | 4 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+30350C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875139 | |||||||
| chr2:47875173 | G | A | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+30316C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875173 | |||||||
| chr2:47875306 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0002g0257 a0001c0001t0002g0272 |
3 | NA18942.hp1 NA19000.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.232+30183G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875306 | |||||||
| chr2:47875310 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0010g0217 |
4 | HG01243.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+30179A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875310 | |||||||
| chr2:47875450 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.232+30039A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875450 | |||||||
| chr2:47875496 | G | A | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+29993C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875496 | |||||||
| chr2:47875498 | CT | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.232+29990delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875498 | |||||||
| chr2:47875709 | C | CT | 5 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+29779dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875709 | |||||||
| chr2:47875951 | A | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0002g0163 |
3 | NA18962.hp2 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.232+29538T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875951 | |||||||
| chr2:47875955 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.232+29534G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875955 | |||||||
| chr2:47875956 | T | C | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+29533A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47875956 | |||||||
| chr2:47876082 | A | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+29407T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876082 | |||||||
| chr2:47876188 | TCTTTTTG others(5): Show |
T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+29289_232+2930 others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876188 | |||||||
| chr2:47876189 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+29300G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876189 | |||||||
| chr2:47876366 | A | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.232+29123T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876366 | |||||||
| chr2:47876372 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0104 others(38): Show |
42 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.232+29117A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876372 | |||||||
| chr2:47876392 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.232+29097C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876392 | |||||||
| chr2:47876559 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0066 |
2 | HG00639.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.232+28930G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876559 | |||||||
| chr2:47876577 | T | C | 1 | a0002c0003t0001g0013 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.232+28912A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876577 | |||||||
| chr2:47876678 | T | A | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+28811A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876678 | |||||||
| chr2:47876759 | A | G | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+28730T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876759 | |||||||
| chr2:47876875 | T | C | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+28614A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876875 | |||||||
| chr2:47876905 | G | A | 19 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(16): Show |
19 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.232+28584C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876905 | |||||||
| chr2:47876916 | AT | A | 29 | a0001c0001t0001g0099 a0001c0001t0001g0160 a0001c0001t0001g0218 others(26): Show |
30 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.232+28572delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876916 | |||||||
| chr2:47876991 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | NA18946.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.232+28498A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47876991 | |||||||
| chr2:47877007 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+28482A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877007 | |||||||
| chr2:47877020 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.232+28469T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877020 | |||||||
| chr2:47877042 | G | GT | 17 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0041 others(14): Show |
17 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.232+28446dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877042 | |||||||
| chr2:47877129 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+28360G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877129 | |||||||
| chr2:47877299 | A | C | 11 | a0001c0001t0001g0253 a0001c0001t0002g0244 a0001c0001t0002g0251 others(8): Show |
11 | HG00735.hp1 HG01168.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+28190T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877299 | |||||||
| chr2:47877356 | A | G | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.232+28133T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877356 | |||||||
| chr2:47877384 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.232+28105T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877384 | |||||||
| chr2:47877423 | T | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0101 |
3 | HG02280.hp2 HG02300.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.232+28066A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877423 | |||||||
| chr2:47877619 | C | G | 1 | a0001c0001t0014g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+27870G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877619 | |||||||
| chr2:47877788 | G | A | 3 | a0001c0001t0003g0232 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+27701C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877788 | |||||||
| chr2:47877830 | G | T | 8 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+27659C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877830 | |||||||
| chr2:47877881 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+27608A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877881 | |||||||
| chr2:47877938 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.232+27551G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47877938 | |||||||
| chr2:47878050 | G | T | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+27439C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878050 | |||||||
| chr2:47878051 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.232+27438A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878051 | |||||||
| chr2:47878317 | T | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG00323.hp2 HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.232+27172A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878317 | |||||||
| chr2:47878355 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+27134A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878355 | |||||||
| chr2:47878479 | C | T | 1 | a0004c0005t0002g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.232+27010G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878479 | |||||||
| chr2:47878510 | C | A | 1 | a0001c0001t0002g0260 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.232+26979G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878510 | |||||||
| chr2:47878517 | G | C | 18 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(15): Show |
18 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.232+26972C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878517 | |||||||
| chr2:47878661 | AT | A | 26 | a0001c0001t0001g0119 a0001c0001t0001g0160 a0001c0001t0001g0165 others(23): Show |
26 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.232+26827delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878661 | |||||||
| chr2:47878706 | G | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+26783C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878706 | |||||||
| chr2:47878749 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.232+26740T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878749 | |||||||
| chr2:47878911 | A | G | 25 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(22): Show |
25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.232+26578T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878911 | |||||||
| chr2:47878964 | T | TCAAAACA others(3): Show |
11 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(8): Show |
11 | HG01346.hp1 HG02145.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+26515_232+2652 others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47878964 | |||||||
| chr2:47879179 | C | A | 2 | a0001c0001t0001g0284 a0001c0001t0002g0292 |
2 | NA18957.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.232+26310G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879179 | |||||||
| chr2:47879243 | T | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+26246A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879243 | |||||||
| chr2:47879251 | A | G | 2 | a0001c0001t0002g0244 a0001c0001t0002g0268 |
2 | HG00735.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.232+26238T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879251 | |||||||
| chr2:47879380 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232+26109C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879380 | |||||||
| chr2:47879557 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0012g0175 a0001c0001t0019g0311 |
3 | NA18952.hp2 NA18965.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.232+25932G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879557 | |||||||
| chr2:47879631 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.232+25858A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879631 | |||||||
| chr2:47879641 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.232+25848C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879641 | |||||||
| chr2:47879676 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.232+25813A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879676 | |||||||
| chr2:47879838 | A | G | 8 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+25651T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879838 | |||||||
| chr2:47879920 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.232+25569G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879920 | |||||||
| chr2:47879940 | C | T | 23 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(20): Show |
23 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.232+25549G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879940 | |||||||
| chr2:47879962 | T | C | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+25527A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47879962 | |||||||
| chr2:47880000 | GT | G | 8 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+25488delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880000 | |||||||
| chr2:47880304 | C | A | 29 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(26): Show |
29 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.232+25185G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880304 | |||||||
| chr2:47880469 | G | C | 1 | a0001c0001t0002g0078 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.232+25020C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880469 | |||||||
| chr2:47880664 | C | T | 5 | a0001c0001t0003g0135 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+24825G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880664 | |||||||
| chr2:47880705 | T | C | 1 | a0001c0001t0002g0056 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.232+24784A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880705 | |||||||
| chr2:47880754 | G | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+24735C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880754 | |||||||
| chr2:47880810 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.232+24679G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880810 | |||||||
| chr2:47880923 | CTAAAGGT others(25): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.232+24534_232+2456 others(36): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880923 | |||||||
| chr2:47880943 | T | C | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+24546A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47880943 | |||||||
| chr2:47881006 | G | C | 5 | a0001c0001t0003g0135 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+24483C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881006 | |||||||
| chr2:47881011 | T | G | 1 | a0001c0001t0001g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.232+24478A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881011 | |||||||
| chr2:47881047 | G | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+24442C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881047 | |||||||
| chr2:47881079 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.232+24410G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881079 | |||||||
| chr2:47881108 | C | T | 1 | a0001c0001t0014g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+24381G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881108 | |||||||
| chr2:47881169 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0030 |
3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.232+24320A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881169 | |||||||
| chr2:47881178 | G | C | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+24311C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881178 | |||||||
| chr2:47881205 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.232+24284A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881205 | |||||||
| chr2:47881221 | C | T | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+24268G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881221 | |||||||
| chr2:47881263 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232+24226C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881263 | |||||||
| chr2:47881322 | G | T | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+24167C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881322 | |||||||
| chr2:47881490 | C | A | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.232+23999G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881490 | |||||||
| chr2:47881647 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.232+23842G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881647 | |||||||
| chr2:47881704 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.232+23785C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881704 | |||||||
| chr2:47881705 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.232+23784A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881705 | |||||||
| chr2:47881754 | C | CT | 126 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 others(123): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.232+23734dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881754 | |||||||
| chr2:47881801 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+23688T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881801 | |||||||
| chr2:47881858 | G | C | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.232+23631C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881858 | |||||||
| chr2:47881880 | T | C | 6 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+23609A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47881880 | |||||||
| chr2:47882130 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+23359G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882130 | |||||||
| chr2:47882182 | A | G | 3 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0002g0247 |
3 | HG01346.hp2 HG01515.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.232+23307T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882182 | |||||||
| chr2:47882368 | C | T | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+23121G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882368 | |||||||
| chr2:47882383 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.232+23106C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882383 | |||||||
| chr2:47882443 | T | TC | 12 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.232+23045dupG | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882443 | |||||||
| chr2:47882474 | C | T | 24 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(21): Show |
24 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.232+23015G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882474 | |||||||
| chr2:47882491 | T | C | 5 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+22998A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882491 | |||||||
| chr2:47882596 | A | G | 1 | a0001c0001t0002g0288 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.232+22893T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882596 | |||||||
| chr2:47882712 | G | A | 5 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+22777C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882712 | |||||||
| chr2:47882780 | T | C | 8 | a0001c0001t0001g0160 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+22709A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882780 | |||||||
| chr2:47882829 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.232+22660A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882829 | |||||||
| chr2:47882886 | C | T | 3 | a0001c0001t0003g0232 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+22603G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47882886 | |||||||
| chr2:47883192 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.232+22297A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883192 | |||||||
| chr2:47883318 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.232+22171G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883318 | |||||||
| chr2:47883410 | C | G | 4 | a0001c0001t0003g0135 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02717.hp1 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+22079G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883410 | |||||||
| chr2:47883425 | A | C | 27 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(24): Show |
27 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.232+22064T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883425 | |||||||
| chr2:47883450 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.232+22039G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883450 | |||||||
| chr2:47883467 | G | C | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+22022C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883467 | |||||||
| chr2:47883701 | T | A | 9 | a0001c0002t0002g0123 a0001c0002t0002g0196 a0001c0002t0002g0197 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+21788A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883701 | |||||||
| chr2:47883715 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.232+21774T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883715 | |||||||
| chr2:47883752 | C | T | 1 | a0001c0001t0010g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232+21737G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883752 | |||||||
| chr2:47883880 | T | C | 5 | a0001c0001t0003g0135 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+21609A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47883880 | |||||||
| chr2:47884057 | T | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(54): Show |
59 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.232+21432A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884057 | |||||||
| chr2:47884281 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.232+21208G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884281 | |||||||
| chr2:47884396 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.232+21093G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884396 | |||||||
| chr2:47884445 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0112 |
2 | HG01993.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.232+21044C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884445 | |||||||
| chr2:47884453 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0002g0289 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.232+21036A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884453 | |||||||
| chr2:47884701 | GGTATTTT others(4): Show |
G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+20777_232+2078 others(15): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884701 | |||||||
| chr2:47884824 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.232+20665A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884824 | |||||||
| chr2:47884828 | CA | C | 7 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+20660delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884828 | |||||||
| chr2:47884880 | C | A | 7 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+20609G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884880 | |||||||
| chr2:47884892 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232+20597T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884892 | |||||||
| chr2:47884914 | A | T | 10 | a0001c0001t0001g0237 a0001c0001t0001g0296 a0001c0001t0002g0236 others(7): Show |
10 | HG00280.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.232+20575T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47884914 | |||||||
| chr2:47885203 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.232+20286A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885203 | |||||||
| chr2:47885332 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.232+20157C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885332 | |||||||
| chr2:47885449 | C | G | 35 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(32): Show |
35 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.232+20040G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885449 | |||||||
| chr2:47885467 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.232+20022G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885467 | |||||||
| chr2:47885515 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.232+19974G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885515 | |||||||
| chr2:47885687 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.232+19802A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885687 | |||||||
| chr2:47885716 | T | C | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+19773A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885716 | |||||||
| chr2:47885789 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+19700T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885789 | |||||||
| chr2:47885974 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.232+19515G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47885974 | |||||||
| chr2:47886007 | A | ATGCATTG others(23): Show |
7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+19481_232+1948 others(34): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886007 | |||||||
| chr2:47886008 | A | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+19481T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886008 | |||||||
| chr2:47886010 | C | G | 5 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(2): Show |
5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+19479G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886010 | |||||||
| chr2:47886265 | G | C | 4 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+19224C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886265 | |||||||
| chr2:47886320 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.232+19169G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886320 | |||||||
| chr2:47886501 | C | CA | 13 | a0001c0001t0001g0131 a0001c0001t0001g0158 a0001c0001t0001g0159 others(10): Show |
13 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.232+18987dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886501 | |||||||
| chr2:47886501 | CA | C | 10 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(7): Show |
10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+18987delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886501 | |||||||
| chr2:47886559 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.232+18930T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886559 | |||||||
| chr2:47886563 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.232+18926A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886563 | |||||||
| chr2:47886693 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+18796T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886693 | |||||||
| chr2:47886778 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.232+18711A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886778 | |||||||
| chr2:47886863 | T | A | 4 | a0001c0001t0001g0063 a0001c0001t0002g0046 a0001c0001t0004g0001 others(1): Show |
5 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+18626A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886863 | |||||||
| chr2:47886864 | G | T | 4 | a0001c0001t0001g0063 a0001c0001t0002g0046 a0001c0001t0004g0001 others(1): Show |
5 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+18625C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886864 | |||||||
| chr2:47886916 | G | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0101 |
3 | HG02280.hp2 HG02300.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.232+18573C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886916 | |||||||
| chr2:47886955 | C | G | 25 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(22): Show |
25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.232+18534G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886955 | |||||||
| chr2:47886972 | C | A | 1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232+18517G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47886972 | |||||||
| chr2:47887070 | G | A | 47 | a0001c0001t0001g0237 a0001c0001t0001g0253 a0001c0001t0001g0256 others(44): Show |
48 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.232+18419C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887070 | |||||||
| chr2:47887195 | T | G | 27 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(24): Show |
27 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.232+18294A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887195 | |||||||
| chr2:47887248 | G | T | 4 | a0001c0001t0002g0261 a0003c0004t0002g0195 a0003c0004t0002g0203 others(1): Show |
4 | HG01884.hp1 HG02896.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+18241C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887248 | |||||||
| chr2:47887299 | G | T | 1 | a0001c0001t0007g0009 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.232+18190C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887299 | |||||||
| chr2:47887450 | C | T | 3 | a0001c0001t0003g0232 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+18039G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887450 | |||||||
| chr2:47887635 | C | T | 7 | a0001c0001t0001g0055 a0001c0001t0001g0077 a0001c0001t0001g0079 others(4): Show |
7 | HG01074.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.232+17854G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47887635 | |||||||
| chr2:47888003 | T | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+17486A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888003 | |||||||
| chr2:47888027 | T | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+17462A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888027 | |||||||
| chr2:47888124 | C | G | 27 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(24): Show |
27 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.232+17365G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888124 | |||||||
| chr2:47888125 | G | A | 9 | a0001c0002t0002g0123 a0001c0002t0002g0196 a0001c0002t0002g0197 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+17364C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888125 | |||||||
| chr2:47888289 | T | C | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+17200A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888289 | |||||||
| chr2:47888577 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.232+16912G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888577 | |||||||
| chr2:47888608 | T | C | 3 | a0003c0004t0002g0195 a0003c0004t0002g0203 a0003c0004t0002g0204 |
3 | HG01884.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.232+16881A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888608 | |||||||
| chr2:47888748 | G | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.232+16741C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888748 | |||||||
| chr2:47888803 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+16686A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888803 | |||||||
| chr2:47888813 | T | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+16676A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888813 | |||||||
| chr2:47888929 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0293 |
3 | HG01243.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.232+16560A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888929 | |||||||
| chr2:47888987 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.232+16502C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47888987 | |||||||
| chr2:47889044 | TTCAC | T | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0149 others(2): Show |
5 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+16441_232+1644 others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889044 | |||||||
| chr2:47889093 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+16396A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889093 | |||||||
| chr2:47889159 | A | G | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG00597.hp1 NA18946.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+16330T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889159 | |||||||
| chr2:47889177 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0004g0001 a0001c0001t0004g0012 |
4 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+16312G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889177 | |||||||
| chr2:47889209 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+16280G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889209 | |||||||
| chr2:47889432 | C | A | 4 | a0001c0001t0003g0232 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+16057G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889432 | |||||||
| chr2:47889496 | T | A | 25 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(22): Show |
25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.232+15993A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889496 | |||||||
| chr2:47889627 | G | A | 1 | a0004c0005t0002g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.232+15862C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889627 | |||||||
| chr2:47889633 | GT | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.232+15855delA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889633 | |||||||
| chr2:47889633 | GTT | G | 12 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(9): Show |
12 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.232+15854_232+1585 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889633 | |||||||
| chr2:47889736 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+15753C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889736 | |||||||
| chr2:47889745 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.232+15744T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47889745 | |||||||
| chr2:47890020 | C | A | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+15469G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890020 | |||||||
| chr2:47890123 | A | ATTAT | 10 | a0001c0001t0001g0119 a0001c0001t0001g0237 a0001c0001t0001g0273 others(7): Show |
10 | HG01261.hp2 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+15362_232+1536 others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890123 | |||||||
| chr2:47890222 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.232+15267G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890222 | |||||||
| chr2:47890235 | A | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+15254T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890235 | |||||||
| chr2:47890292 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.232+15197A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890292 | |||||||
| chr2:47890358 | T | C | 3 | a0001c0001t0001g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+15131A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890358 | |||||||
| chr2:47890436 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.232+15053A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890436 | |||||||
| chr2:47890517 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.232+14972T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890517 | |||||||
| chr2:47890660 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | NA18999.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.232+14829G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890660 | |||||||
| chr2:47890736 | A | T | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+14753T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890736 | |||||||
| chr2:47890777 | C | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+14712G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890777 | |||||||
| chr2:47890787 | G | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG01433.hp1 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.232+14702C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890787 | |||||||
| chr2:47890791 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+14698C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890791 | |||||||
| chr2:47890811 | GA | G | 28 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(25): Show |
28 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.232+14677delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890811 | |||||||
| chr2:47890821 | A | T | 1 | a0001c0001t0002g0168 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+14668T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890821 | |||||||
| chr2:47890826 | T | G | 4 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+14663A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890826 | |||||||
| chr2:47890855 | T | C | 1 | a0001c0001t0002g0267 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.232+14634A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890855 | |||||||
| chr2:47890875 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.232+14614A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890875 | |||||||
| chr2:47890901 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.232+14588A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890901 | |||||||
| chr2:47890994 | T | A | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+14495A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890994 | |||||||
| chr2:47890994 | T | TTA | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+14494_232+1449 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890994 | |||||||
| chr2:47890996 | A | AT | 19 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(16): Show |
19 | HG00738.hp1 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.232+14492dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890996 | |||||||
| chr2:47890996 | A | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+14493T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47890996 | |||||||
| chr2:47891481 | G | A | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+14008C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891481 | |||||||
| chr2:47891499 | T | C | 3 | a0001c0001t0001g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+13990A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891499 | |||||||
| chr2:47891590 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | NA18946.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.232+13899A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891590 | |||||||
| chr2:47891676 | A | T | 1 | a0001c0001t0002g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.232+13813T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891676 | |||||||
| chr2:47891678 | T | A | 1 | a0001c0001t0002g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.232+13811A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891678 | |||||||
| chr2:47891749 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0157 |
2 | HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.232+13740C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891749 | |||||||
| chr2:47891757 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(50): Show |
55 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.232+13732A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47891757 | |||||||
| chr2:47892096 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+13393A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892096 | |||||||
| chr2:47892117 | T | A | 1 | a0001c0001t0002g0163 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.232+13372A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892117 | |||||||
| chr2:47892134 | C | T | 50 | a0001c0001t0001g0237 a0001c0001t0001g0253 a0001c0001t0001g0256 others(47): Show |
51 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.232+13355G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892134 | |||||||
| chr2:47892278 | T | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+13211A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892278 | |||||||
| chr2:47892307 | A | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+13182T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892307 | |||||||
| chr2:47892363 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.232+13126A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892363 | |||||||
| chr2:47892524 | T | A | 3 | a0001c0001t0001g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+12965A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892524 | |||||||
| chr2:47892531 | G | T | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.232+12958C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892531 | |||||||
| chr2:47892641 | A | T | 4 | a0001c0001t0003g0232 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+12848T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892641 | |||||||
| chr2:47892698 | A | G | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+12791T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892698 | |||||||
| chr2:47892763 | G | C | 1 | a0001c0001t0007g0009 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.232+12726C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892763 | |||||||
| chr2:47892791 | A | G | 1 | a0001c0001t0002g0288 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.232+12698T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892791 | |||||||
| chr2:47892821 | T | C | 5 | a0001c0001t0003g0135 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+12668A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892821 | |||||||
| chr2:47892856 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.232+12633G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892856 | |||||||
| chr2:47892949 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 others(106): Show |
110 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.232+12540A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47892949 | |||||||
| chr2:47893019 | G | T | 25 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(22): Show |
25 | HG00438.hp1 HG00544.hp1 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.232+12470C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893019 | |||||||
| chr2:47893042 | C | G | 4 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0282 others(1): Show |
4 | HG02027.hp1 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+12447G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893042 | |||||||
| chr2:47893048 | C | G | 3 | a0001c0001t0001g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+12441G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893048 | |||||||
| chr2:47893107 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.232+12382A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893107 | |||||||
| chr2:47893166 | T | TTAAATAA others(5): Show |
6 | a0001c0001t0001g0229 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01257.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+12311_232+1232 others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893166 | |||||||
| chr2:47893166 | T | TTAAATAA others(9): Show |
4 | a0001c0001t0001g0228 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG01081.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+12307_232+1232 others(20): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893166 | |||||||
| chr2:47893166 | T | TTAAATAA others(13): Show |
5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG00280.hp2 HG01070.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+12303_232+1232 others(24): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893166 | |||||||
| chr2:47893178 | A | ATAAATAA others(5): Show |
9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+12310_232+1231 others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893178 | |||||||
| chr2:47893178 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.232+12311T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893178 | |||||||
| chr2:47893281 | C | T | 6 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0002g0167 others(3): Show |
6 | HG01261.hp2 HG01891.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+12208G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893281 | |||||||
| chr2:47893353 | C | CAT | 4 | a0001c0001t0001g0077 a0001c0001t0001g0275 a0001c0001t0002g0276 others(1): Show |
4 | HG01074.hp2 NA19005.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+12134_232+1213 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893353 | |||||||
| chr2:47893353 | CAT | C | 20 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(17): Show |
20 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.232+12134_232+1213 others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893353 | |||||||
| chr2:47893367 | T | C | 8 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+12122A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893367 | |||||||
| chr2:47893381 | A | C | 1 | a0001c0001t0002g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.232+12108T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893381 | |||||||
| chr2:47893559 | G | C | 21 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(18): Show |
21 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.232+11930C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893559 | |||||||
| chr2:47893678 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.232+11811C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893678 | |||||||
| chr2:47893679 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.232+11810G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893679 | |||||||
| chr2:47893727 | G | A | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+11762C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893727 | |||||||
| chr2:47893992 | G | C | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0218 others(6): Show |
9 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+11497C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47893992 | |||||||
| chr2:47894049 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0110 |
2 | HG01169.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.232+11440A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894049 | |||||||
| chr2:47894464 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+11025A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894464 | |||||||
| chr2:47894571 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232+10918T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894571 | |||||||
| chr2:47894577 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+10912G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894577 | |||||||
| chr2:47894606 | A | C | 4 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0282 others(1): Show |
4 | HG02027.hp1 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+10883T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894606 | |||||||
| chr2:47894855 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0002g0046 a0001c0001t0004g0001 others(1): Show |
5 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+10634A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894855 | |||||||
| chr2:47894925 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232+10564G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47894925 | |||||||
| chr2:47895107 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.232+10382T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895107 | |||||||
| chr2:47895115 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.232+10374A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895115 | |||||||
| chr2:47895122 | G | C | 6 | a0001c0001t0003g0121 a0001c0001t0003g0135 a0001c0001t0003g0232 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+10367C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895122 | |||||||
| chr2:47895137 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232+10352C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895137 | |||||||
| chr2:47895238 | C | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG01891.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.232+10251G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895238 | |||||||
| chr2:47895418 | G | T | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+10071C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895418 | |||||||
| chr2:47895540 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+9949A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895540 | |||||||
| chr2:47895582 | G | A | 9 | a0001c0002t0002g0123 a0001c0002t0002g0196 a0001c0002t0002g0197 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+9907C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895582 | |||||||
| chr2:47895684 | A | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG01891.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.232+9805T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895684 | |||||||
| chr2:47895703 | T | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0303 |
4 | HG02055.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+9786A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895703 | |||||||
| chr2:47895709 | T | C | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+9780A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895709 | |||||||
| chr2:47895752 | G | T | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+9737C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895752 | |||||||
| chr2:47895818 | G | A | 3 | a0001c0001t0001g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG01074.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+9671C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895818 | |||||||
| chr2:47895883 | G | A | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+9606C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895883 | |||||||
| chr2:47895903 | G | C | 4 | a0001c0001t0001g0063 a0001c0001t0002g0046 a0001c0001t0004g0001 others(1): Show |
5 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+9586C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895903 | |||||||
| chr2:47895930 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+9559G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895930 | |||||||
| chr2:47895954 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232+9535G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895954 | |||||||
| chr2:47895990 | C | T | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+9499G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47895990 | |||||||
| chr2:47896016 | T | G | 1 | a0001c0001t0002g0263 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.232+9473A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896016 | |||||||
| chr2:47896247 | T | C | 22 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(19): Show |
22 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+9242A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896247 | |||||||
| chr2:47896321 | G | GTTTCT | 19 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(16): Show |
19 | HG01346.hp1 HG02145.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.232+9163_232+9167d others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896321 | |||||||
| chr2:47896330 | C | CT | 18 | a0001c0001t0001g0053 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.232+9158dupA | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896330 | |||||||
| chr2:47896330 | C | CTTTTCT | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+9158_232+9159i others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896330 | |||||||
| chr2:47896491 | C | G | 2 | a0001c0001t0002g0124 a0001c0002t0002g0123 |
2 | HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.232+8998G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896491 | |||||||
| chr2:47896540 | G | C | 6 | a0001c0001t0002g0264 a0001c0001t0002g0265 a0001c0001t0002g0285 others(3): Show |
6 | HG01884.hp1 HG01978.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+8949C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896540 | |||||||
| chr2:47896611 | C | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0268 |
2 | HG00735.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.232+8878G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896611 | |||||||
| chr2:47896613 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.232+8876A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896613 | |||||||
| chr2:47896720 | T | C | 6 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+8769A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896720 | |||||||
| chr2:47896749 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.232+8740C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896749 | |||||||
| chr2:47896756 | A | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+8733T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896756 | |||||||
| chr2:47896766 | G | A | 1 | a0001c0001t0014g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+8723C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896766 | |||||||
| chr2:47896776 | A | T | 31 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(28): Show |
31 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.232+8713T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896776 | |||||||
| chr2:47896931 | A | C | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.232+8558T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47896931 | |||||||
| chr2:47897039 | G | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(7): Show |
10 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+8450C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897039 | |||||||
| chr2:47897088 | A | C | 2 | a0001c0001t0001g0137 a0002c0003t0001g0014 |
2 | HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.232+8401T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897088 | |||||||
| chr2:47897090 | A | C | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.232+8399T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897090 | |||||||
| chr2:47897365 | G | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0032 others(97): Show |
102 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.232+8124C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897365 | |||||||
| chr2:47897525 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.232+7964G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897525 | |||||||
| chr2:47897563 | G | T | 1 | a0001c0001t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.232+7926C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897563 | |||||||
| chr2:47897616 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.232+7873C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897616 | |||||||
| chr2:47897701 | C | CA | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(72): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.232+7787dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897701 | |||||||
| chr2:47897701 | CA | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0032 others(90): Show |
95 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.232+7787delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897701 | |||||||
| chr2:47897930 | A | C | 1 | a0003c0004t0002g0195 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.232+7559T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47897930 | |||||||
| chr2:47898009 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.232+7480A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898009 | |||||||
| chr2:47898097 | T | C | 1 | a0001c0001t0007g0009 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.232+7392A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898097 | |||||||
| chr2:47898154 | A | G | 2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.232+7335T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898154 | |||||||
| chr2:47898288 | A | G | 1 | a0001c0001t0008g0010 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.232+7201T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898288 | |||||||
| chr2:47898361 | T | C | 6 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+7128A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898361 | |||||||
| chr2:47898399 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.232+7090T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898399 | |||||||
| chr2:47898569 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.232+6920G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898569 | |||||||
| chr2:47898589 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.232+6900T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898589 | |||||||
| chr2:47898692 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.232+6797T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898692 | |||||||
| chr2:47898784 | G | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+6705C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47898784 | |||||||
| chr2:47899002 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.232+6487G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899002 | |||||||
| chr2:47899059 | G | C | 3 | a0001c0001t0003g0232 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+6430C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899059 | |||||||
| chr2:47899147 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.232+6342T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899147 | |||||||
| chr2:47899223 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.232+6266C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899223 | |||||||
| chr2:47899263 | G | C | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+6226C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899263 | |||||||
| chr2:47899273 | C | CA | 33 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(30): Show |
33 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.232+6215dupT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899273 | |||||||
| chr2:47899273 | CA | C | 13 | a0001c0001t0001g0031 a0001c0001t0001g0065 a0001c0001t0001g0073 others(10): Show |
13 | HG00280.hp1 HG00609.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.232+6215delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899273 | |||||||
| chr2:47899357 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0112 |
2 | HG01993.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.232+6132A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899357 | |||||||
| chr2:47899397 | C | G | 1 | a0001c0001t0002g0046 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.232+6092G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899397 | |||||||
| chr2:47899455 | A | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.232+6034T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899455 | |||||||
| chr2:47899600 | T | G | 34 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0159 others(31): Show |
35 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.232+5889A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899600 | |||||||
| chr2:47899619 | C | T | 1 | a0001c0001t0008g0010 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.232+5870G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899619 | |||||||
| chr2:47899682 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.232+5807C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899682 | |||||||
| chr2:47899682 | G | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0002g0163 |
3 | NA18962.hp2 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.232+5807C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899682 | |||||||
| chr2:47899811 | C | A | 1 | a0001c0001t0002g0272 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.232+5678G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899811 | |||||||
| chr2:47899837 | C | A | 1 | a0001c0001t0002g0272 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.232+5652G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899837 | |||||||
| chr2:47899926 | T | C | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG00621.hp1 HG01993.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+5563A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47899926 | |||||||
| chr2:47900116 | C | A | 19 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(16): Show |
19 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.232+5373G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900116 | |||||||
| chr2:47900121 | T | C | 7 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+5368A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900121 | |||||||
| chr2:47900133 | T | A | 5 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(2): Show |
5 | HG01074.hp2 HG01891.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+5356A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900133 | |||||||
| chr2:47900173 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.232+5316A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900173 | |||||||
| chr2:47900182 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0164 |
3 | HG00099.hp1 HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.232+5307A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900182 | |||||||
| chr2:47900192 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232+5297T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900192 | |||||||
| chr2:47900199 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.232+5290A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900199 | |||||||
| chr2:47900423 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.232+5066T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900423 | |||||||
| chr2:47900450 | A | C | 1 | a0001c0001t0002g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.232+5039T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900450 | |||||||
| chr2:47900553 | TACACGTA others(7): Show |
T | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4922_232+4935d others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900553 | |||||||
| chr2:47900557 | C | CGTATATA others(19): Show |
7 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4931_232+4932i others(28): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900557 | |||||||
| chr2:47900557 | C | CGTATATA others(45): Show |
1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232+4931_232+4932i others(54): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900557 | |||||||
| chr2:47900558 | G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.232+4903_232+4930d others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900558 | |||||||
| chr2:47900560 | ATATATAC others(73): Show |
A | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.232+4849_232+4928d others(82): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900560 | |||||||
| chr2:47900565 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4924A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900565 | |||||||
| chr2:47900575 | T | TATACGTG others(21): Show |
1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+4913_232+4914i others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900575 | |||||||
| chr2:47900577 | C | CACGTGTG others(153): Show |
2 | a0001c0001t0001g0227 a0001c0001t0001g0230 |
2 | HG01255.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.232+4911_232+4912i others(162): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | |||||||
| chr2:47900577 | C | CACGTGTG others(181): Show |
1 | a0001c0001t0001g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.232+4911_232+4912i others(190): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | |||||||
| chr2:47900577 | C | CACGTGTG others(209): Show |
2 | a0001c0001t0001g0225 a0001c0001t0001g0231 |
2 | HG00280.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.232+4911_232+4912i others(218): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | |||||||
| chr2:47900577 | C | CACGTGTG others(237): Show |
1 | a0001c0001t0001g0226 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.232+4911_232+4912i others(246): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | |||||||
| chr2:47900577 | C | CACGTGTG others(154): Show |
1 | a0001c0001t0001g0229 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.232+4911_232+4912i others(163): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | |||||||
| chr2:47900577 | C | T | 3 | a0001c0001t0003g0121 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4912G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900577 | |||||||
| chr2:47900580 | A | G | 1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+4909T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900580 | |||||||
| chr2:47900581 | C | T | 3 | a0001c0001t0003g0121 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4908G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900581 | |||||||
| chr2:47900583 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4906A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900583 | |||||||
| chr2:47900585 | T | C | 9 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(6): Show |
9 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+4904A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900585 | |||||||
| chr2:47900586 | A | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4903T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900586 | |||||||
| chr2:47900586 | ATACGTAT others(43): Show |
A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0030 |
3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.232+4853_232+4902d others(52): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900586 | |||||||
| chr2:47900587 | T | C | 4 | a0001c0001t0003g0121 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4902A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900587 | |||||||
| chr2:47900587 | TACGTATA others(15): Show |
T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG02080.hp1 NA18747.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.232+4880_232+4901d others(24): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900587 | |||||||
| chr2:47900590 | G | A | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4899C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900590 | |||||||
| chr2:47900591 | T | C | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4898A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900591 | |||||||
| chr2:47900592 | A | G | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4897T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900592 | |||||||
| chr2:47900595 | T | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(20): Show |
23 | HG00738.hp1 HG01109.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.232+4894A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900595 | |||||||
| chr2:47900602 | GTATACAC others(5): Show |
G | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.232+4875_232+4886d others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900602 | |||||||
| chr2:47900603 | T | C | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.232+4886A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900603 | |||||||
| chr2:47900607 | C | T | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4882G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900607 | |||||||
| chr2:47900609 | C | CACACGT | 19 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(16): Show |
19 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.232+4879_232+4880i others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900609 | |||||||
| chr2:47900609 | C | CACGTATA others(9): Show |
3 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01346.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4879_232+4880i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900609 | |||||||
| chr2:47900609 | CACGTATA others(21): Show |
C | 23 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(20): Show |
23 | HG01069.hp2 HG01168.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.232+4852_232+4879d others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900609 | |||||||
| chr2:47900612 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4877C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900612 | |||||||
| chr2:47900613 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4876A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900613 | |||||||
| chr2:47900614 | A | G | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4875T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900614 | |||||||
| chr2:47900617 | T | C | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0073 others(8): Show |
11 | HG00609.hp2 HG00639.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+4872A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900617 | |||||||
| chr2:47900617 | T | TACACACG others(9): Show |
1 | a0001c0001t0001g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.232+4871_232+4872i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900617 | |||||||
| chr2:47900617 | TACACACG others(5): Show |
T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0297 a0001c0001t0007g0009 |
3 | HG03669.hp1 HG04204.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.232+4860_232+4871d others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900617 | |||||||
| chr2:47900621 | C | CACGT | 28 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(25): Show |
29 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.232+4864_232+4867d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900621 | |||||||
| chr2:47900625 | T | C | 1 | a0001c0001t0003g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+4864A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900625 | |||||||
| chr2:47900625 | TATACACA others(17): Show |
T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0165 a0001c0001t0001g0299 |
3 | HG00639.hp2 NA18991.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.232+4840_232+4863d others(26): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900625 | |||||||
| chr2:47900626 | A | ACG | 44 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0037 others(41): Show |
45 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.232+4862_232+4863i others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900626 | |||||||
| chr2:47900627 | TACACACA others(33): Show |
T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0216 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.232+4822_232+4861d others(42): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900627 | |||||||
| chr2:47900629 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0037 others(59): Show |
64 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.232+4860G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900629 | |||||||
| chr2:47900631 | C | CGTACGTA others(61): Show |
1 | a0001c0001t0003g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+4857_232+4858i others(70): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900631 | |||||||
| chr2:47900631 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0113 a0001c0001t0003g0300 others(1): Show |
4 | HG02027.hp2 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4858G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900631 | |||||||
| chr2:47900635 | CGT | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0037 others(42): Show |
46 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.232+4852_232+4853d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900635 | |||||||
| chr2:47900637 | T | TATACACA others(1): Show |
27 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
28 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.232+4851_232+4852i others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900637 | |||||||
| chr2:47900639 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.232+4850G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900639 | |||||||
| chr2:47900640 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0002g0034 |
2 | HG03927.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.232+4849C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900640 | |||||||
| chr2:47900641 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.232+4848A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900641 | |||||||
| chr2:47900642 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.232+4847T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900642 | |||||||
| chr2:47900645 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0031 others(78): Show |
83 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.232+4844A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900645 | |||||||
| chr2:47900645 | TACACACG others(33): Show |
T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.232+4804_232+4843d others(42): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900645 | |||||||
| chr2:47900647 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+4842G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900647 | |||||||
| chr2:47900647 | CACACGTA others(61): Show |
C | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232+4774_232+4841d others(70): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900647 | |||||||
| chr2:47900649 | C | CGT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0084 others(6): Show |
10 | HG00544.hp2 HG00597.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.232+4839_232+4840i others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900649 | |||||||
| chr2:47900652 | GTATA | G | 5 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4833_232+4836d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900652 | |||||||
| chr2:47900654 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG03831.hp1 NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4835T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900654 | |||||||
| chr2:47900655 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+4834A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900655 | |||||||
| chr2:47900657 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0165 a0001c0001t0001g0294 others(1): Show |
4 | HG00639.hp2 HG03831.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4832G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900657 | |||||||
| chr2:47900657 | CACACACG others(9): Show |
C | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+4816_232+4831d others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900657 | |||||||
| chr2:47900659 | C | T | 8 | a0001c0001t0001g0093 a0001c0001t0001g0294 a0001c0001t0001g0295 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4830G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900659 | |||||||
| chr2:47900659 | CACACGTA others(49): Show |
C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0146 others(6): Show |
10 | HG02055.hp2 HG03130.hp1 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+4774_232+4829d others(58): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900659 | |||||||
| chr2:47900659 | CACACGTA others(77): Show |
C | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.232+4746_232+4829d others(86): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900659 | |||||||
| chr2:47900661 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.232+4828G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900661 | |||||||
| chr2:47900661 | C | T | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4828G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900661 | |||||||
| chr2:47900661 | CACGT | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0043 others(109): Show |
113 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.232+4824_232+4827d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900661 | |||||||
| chr2:47900663 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG03831.hp1 NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4826G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900663 | |||||||
| chr2:47900664 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG03831.hp1 NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4825C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900664 | |||||||
| chr2:47900665 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG03831.hp1 NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+4824A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | |||||||
| chr2:47900665 | T | TATACACA others(57): Show |
1 | a0001c0001t0001g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232+4823_232+4824i others(66): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | |||||||
| chr2:47900665 | T | TATACACA others(17): Show |
6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+4823_232+4824i others(26): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | |||||||
| chr2:47900665 | T | TATACACA others(45): Show |
2 | a0001c0002t0002g0198 a0001c0002t0002g0202 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.232+4823_232+4824i others(54): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | |||||||
| chr2:47900665 | T | TGTATATA others(7): Show |
1 | a0001c0001t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.232+4823_232+4824i others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | |||||||
| chr2:47900665 | TAC | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0115 others(5): Show |
8 | HG00099.hp1 HG00099.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4822_232+4823d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | |||||||
| chr2:47900665 | TACGTATA others(5): Show |
T | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4812_232+4823d others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900665 | |||||||
| chr2:47900666 | A | G | 33 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(30): Show |
34 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.232+4823T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900666 | |||||||
| chr2:47900667 | C | T | 35 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(32): Show |
36 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.232+4822G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900667 | |||||||
| chr2:47900668 | G | A | 35 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(32): Show |
36 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.232+4821C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900668 | |||||||
| chr2:47900668 | G | GTA | 5 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(2): Show |
5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4819_232+4820d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900668 | |||||||
| chr2:47900668 | G | GTATATAC others(93): Show |
1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+4820_232+4821i others(102): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900668 | |||||||
| chr2:47900673 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(139): Show |
143 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.232+4816A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900673 | |||||||
| chr2:47900674 | ACACACG | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0115 others(5): Show |
8 | HG00099.hp1 HG00099.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4809_232+4814d others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900674 | |||||||
| chr2:47900675 | C | T | 38 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(35): Show |
39 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.232+4814G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900675 | |||||||
| chr2:47900678 | A | ACGTATAC others(9): Show |
1 | a0001c0001t0014g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+4810_232+4811i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900678 | |||||||
| chr2:47900678 | A | G | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | HG00738.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.232+4811T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900678 | |||||||
| chr2:47900680 | G | GTATATAT others(53): Show |
12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(9): Show |
12 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.232+4808_232+4809i others(62): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900680 | |||||||
| chr2:47900680 | G | GTATATAT others(81): Show |
1 | a0001c0001t0001g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.232+4808_232+4809i others(90): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900680 | |||||||
| chr2:47900680 | G | GTGTA | 122 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0038 others(119): Show |
123 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.232+4808_232+4809i others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900680 | |||||||
| chr2:47900680 | G | GTGTATAT others(53): Show |
1 | a0001c0001t0001g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.232+4808_232+4809i others(62): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900680 | |||||||
| chr2:47900681 | T | C | 4 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4808A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900681 | |||||||
| chr2:47900683 | TACAC | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0115 others(5): Show |
8 | HG00099.hp1 HG00099.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4802_232+4805d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900683 | |||||||
| chr2:47900685 | C | CACACACG others(9): Show |
7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4803_232+4804i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | |||||||
| chr2:47900685 | C | CACACACG others(39): Show |
1 | a0001c0001t0001g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.232+4803_232+4804i others(48): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | |||||||
| chr2:47900685 | C | CACACACG others(67): Show |
3 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG01346.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4803_232+4804i others(76): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | |||||||
| chr2:47900685 | C | CACACACG others(95): Show |
1 | a0001c0001t0001g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.232+4803_232+4804i others(104): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | |||||||
| chr2:47900685 | C | CACACACG others(99): Show |
1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232+4803_232+4804i others(108): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | |||||||
| chr2:47900685 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.232+4804G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | |||||||
| chr2:47900685 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(133): Show |
137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.232+4804G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900685 | |||||||
| chr2:47900687 | C | CACACGTA others(119): Show |
1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+4801_232+4802i others(128): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | |||||||
| chr2:47900687 | C | CACACGTG others(9): Show |
21 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0067 others(18): Show |
22 | HG00323.hp1 HG00597.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+4801_232+4802i others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | |||||||
| chr2:47900687 | C | CACACGTG others(37): Show |
14 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0064 others(11): Show |
14 | HG00609.hp2 HG00621.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+4801_232+4802i others(46): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | |||||||
| chr2:47900687 | C | CACACGTG others(65): Show |
1 | a0001c0001t0001g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+4801_232+4802i others(74): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | |||||||
| chr2:47900687 | C | CACACGTG others(93): Show |
2 | a0001c0001t0001g0036 a0001c0001t0002g0169 |
2 | HG02055.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.232+4801_232+4802i others(102): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | |||||||
| chr2:47900687 | C | CGTACGTA others(21): Show |
1 | a0004c0005t0002g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.232+4801_232+4802i others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | |||||||
| chr2:47900687 | C | CGTACGTA others(225): Show |
1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232+4801_232+4802i others(234): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | |||||||
| chr2:47900687 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(133): Show |
137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.232+4802G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900687 | |||||||
| chr2:47900688 | A | G | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4801T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900688 | |||||||
| chr2:47900689 | C | T | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4800G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900689 | |||||||
| chr2:47900693 | T | TGTATATA others(205): Show |
1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4795_232+4796i others(214): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900693 | |||||||
| chr2:47900697 | C | T | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.232+4792G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900697 | |||||||
| chr2:47900705 | T | C | 3 | a0001c0001t0001g0113 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02027.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4784A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900705 | |||||||
| chr2:47900706 | G | A | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4783C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900706 | |||||||
| chr2:47900706 | G | GTA | 3 | a0001c0001t0002g0094 a0001c0001t0004g0001 a0001c0001t0004g0012 |
4 | HG02135.hp2 HG02523.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4781_232+4782d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900706 | |||||||
| chr2:47900707 | T | C | 4 | a0001c0001t0002g0124 a0001c0001t0002g0126 a0001c0001t0014g0127 others(1): Show |
4 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4782A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900707 | |||||||
| chr2:47900708 | A | ACACGTAC others(97): Show |
1 | a0001c0001t0003g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.232+4780_232+4781i others(106): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900708 | |||||||
| chr2:47900708 | A | ATACACAC others(47): Show |
1 | a0001c0001t0002g0125 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.232+4780_232+4781i others(56): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900708 | |||||||
| chr2:47900708 | A | G | 4 | a0001c0001t0002g0124 a0001c0001t0002g0126 a0001c0001t0014g0127 others(1): Show |
4 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4781T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900708 | |||||||
| chr2:47900713 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4776A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900713 | |||||||
| chr2:47900715 | T | C | 21 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(18): Show |
21 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.232+4774A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900715 | |||||||
| chr2:47900721 | T | C | 1 | a0001c0001t0003g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.232+4768A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900721 | |||||||
| chr2:47900728 | A | G | 1 | a0001c0001t0003g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+4761T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900728 | |||||||
| chr2:47900729 | C | T | 1 | a0001c0001t0003g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+4760G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900729 | |||||||
| chr2:47900733 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.232+4756A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900733 | |||||||
| chr2:47900735 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4754A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900735 | |||||||
| chr2:47900736 | A | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4753T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900736 | |||||||
| chr2:47900740 | A | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4749T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900740 | |||||||
| chr2:47900741 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4748A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900741 | |||||||
| chr2:47900743 | T | C | 22 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(19): Show |
22 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+4746A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900743 | |||||||
| chr2:47900761 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.232+4728A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900761 | |||||||
| chr2:47900763 | T | C | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0014g0127 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4726A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900763 | |||||||
| chr2:47900764 | A | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4725T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900764 | |||||||
| chr2:47900769 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4720A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900769 | |||||||
| chr2:47900771 | T | C | 22 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(19): Show |
22 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+4718A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900771 | |||||||
| chr2:47900789 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.232+4700A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900789 | |||||||
| chr2:47900791 | T | C | 3 | a0001c0001t0002g0124 a0001c0001t0014g0127 a0001c0002t0002g0123 |
3 | HG01109.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.232+4698A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900791 | |||||||
| chr2:47900792 | A | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4697T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900792 | |||||||
| chr2:47900797 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4692A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900797 | |||||||
| chr2:47900799 | T | C | 21 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(18): Show |
21 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.232+4690A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900799 | |||||||
| chr2:47900809 | CACACACG others(19): Show |
C | 6 | a0001c0001t0001g0284 a0001c0001t0002g0281 a0001c0001t0002g0282 others(3): Show |
6 | HG02080.hp1 HG04228.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4654_232+4679d others(28): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900809 | |||||||
| chr2:47900818 | GTA | G | 5 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0228 others(2): Show |
5 | HG00280.hp2 HG01081.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4669_232+4670d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900818 | |||||||
| chr2:47900820 | A | ATATACAC others(71): Show |
1 | a0001c0001t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.232+4668_232+4669i others(80): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900820 | |||||||
| chr2:47900820 | A | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4669T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900820 | |||||||
| chr2:47900825 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4664A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900825 | |||||||
| chr2:47900827 | T | C | 16 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(13): Show |
16 | HG00738.hp1 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+4662A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900827 | |||||||
| chr2:47900832 | G | GTA | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+4655_232+4656d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900832 | |||||||
| chr2:47900832 | G | GTATACAC others(21): Show |
1 | a0001c0001t0001g0225 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.232+4656_232+4657i others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900832 | |||||||
| chr2:47900832 | G | GTATACAC others(23): Show |
1 | a0001c0001t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.232+4627_232+4656d others(32): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900832 | |||||||
| chr2:47900835 | T | TAC | 119 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(116): Show |
120 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.232+4652_232+4653d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | |||||||
| chr2:47900835 | T | TACACACA others(25): Show |
1 | a0001c0001t0001g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.232+4653_232+4654i others(34): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | |||||||
| chr2:47900835 | T | TACACACA others(23): Show |
7 | a0001c0001t0002g0235 a0001c0001t0002g0259 a0001c0002t0002g0196 others(4): Show |
7 | HG01099.hp1 HG01175.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.232+4624_232+4653d others(32): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | |||||||
| chr2:47900835 | T | TACACACA others(53): Show |
2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.232+4653_232+4654i others(62): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | |||||||
| chr2:47900835 | T | TACACACA others(51): Show |
1 | a0001c0002t0002g0197 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.232+4653_232+4654i others(60): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900835 | |||||||
| chr2:47900844 | G | GTGTATAT others(79): Show |
3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0231 |
3 | HG01070.hp1 HG01516.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.232+4644_232+4645i others(88): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900844 | |||||||
| chr2:47900844 | G | GTGTATAT others(53): Show |
3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG01081.hp1 HG01255.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.232+4644_232+4645i others(62): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900844 | |||||||
| chr2:47900846 | GTA | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02723.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4641_232+4642d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900846 | |||||||
| chr2:47900848 | A | G | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4641T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900848 | |||||||
| chr2:47900853 | T | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4636A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900853 | |||||||
| chr2:47900855 | T | C | 6 | a0001c0001t0001g0218 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4634A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900855 | |||||||
| chr2:47900860 | G | GTA | 10 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(7): Show |
10 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+4627_232+4628d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900860 | |||||||
| chr2:47900860 | G | GTATACAC others(57): Show |
1 | a0001c0001t0002g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.232+4628_232+4629i others(66): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900860 | |||||||
| chr2:47900860 | G | GTATACAC others(23): Show |
3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02723.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4628_232+4629i others(32): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900860 | |||||||
| chr2:47900863 | TAC | T | 3 | a0001c0001t0001g0218 a0001c0001t0003g0121 a0001c0001t0003g0300 |
3 | HG01346.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.232+4624_232+4625d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900863 | |||||||
| chr2:47900865 | C | CACACACA others(23): Show |
33 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0062 others(30): Show |
35 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.232+4594_232+4623d others(32): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(51): Show |
7 | a0001c0001t0001g0290 a0001c0001t0002g0005 a0001c0001t0002g0233 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+4623_232+4624i others(60): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(101): Show |
1 | a0001c0001t0001g0205 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.232+4623_232+4624i others(110): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(79): Show |
2 | a0001c0001t0001g0192 a0001c0001t0015g0211 |
2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.232+4623_232+4624i others(88): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(77): Show |
1 | a0001c0001t0001g0159 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.232+4623_232+4624i others(86): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(77): Show |
1 | a0001c0001t0001g0184 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.232+4623_232+4624i others(86): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(49): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0293 |
3 | HG01243.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.232+4623_232+4624i others(58): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(21): Show |
12 | a0001c0001t0001g0052 a0001c0001t0001g0116 a0001c0001t0001g0173 others(9): Show |
12 | HG00438.hp1 HG00544.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.232+4623_232+4624i others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(51): Show |
1 | a0001c0001t0001g0043 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.232+4623_232+4624i others(60): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | CACACACG others(49): Show |
1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.232+4623_232+4624i others(58): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900865 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.232+4624G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900865 | |||||||
| chr2:47900867 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.232+4622G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900867 | |||||||
| chr2:47900872 | A | G | 3 | a0001c0001t0003g0232 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4617T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900872 | |||||||
| chr2:47900873 | C | CGT | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4614_232+4615d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900873 | |||||||
| chr2:47900873 | C | T | 16 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(13): Show |
16 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.232+4616G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900873 | |||||||
| chr2:47900874 | G | A | 13 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(10): Show |
13 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.232+4615C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900874 | |||||||
| chr2:47900874 | G | GTGTATAT others(51): Show |
1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+4614_232+4615i others(60): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900874 | |||||||
| chr2:47900876 | G | A | 3 | a0001c0001t0003g0232 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.232+4613C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900876 | |||||||
| chr2:47900880 | A | ATATATAC others(3): Show |
1 | a0001c0001t0003g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232+4599_232+4608d others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900880 | |||||||
| chr2:47900880 | A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+4608_232+4609i others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900880 | |||||||
| chr2:47900883 | T | C | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4606A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900883 | |||||||
| chr2:47900885 | T | TACACGTA others(3): Show |
1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4603_232+4604i others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900885 | |||||||
| chr2:47900892 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.232+4597T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900892 | |||||||
| chr2:47900897 | T | C | 14 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(11): Show |
14 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.232+4592A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900897 | |||||||
| chr2:47900903 | CAT | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(2): Show |
5 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+4584_232+4585d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900903 | |||||||
| chr2:47900912 | G | GTATA | 4 | a0001c0001t0003g0232 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+4573_232+4576d others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900912 | |||||||
| chr2:47900951 | A | T | 1 | a0001c0001t0002g0272 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.232+4538T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900951 | |||||||
| chr2:47900998 | G | A | 1 | a0001c0001t0013g0287 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.232+4491C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47900998 | |||||||
| chr2:47901014 | T | C | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4475A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901014 | |||||||
| chr2:47901018 | TATGTATA others(103): Show |
T | 35 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(32): Show |
35 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.232+4361_232+4470d others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901018 | |||||||
| chr2:47901037 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0030 |
3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.232+4452C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901037 | |||||||
| chr2:47901052 | C | T | 24 | a0001c0001t0001g0122 a0001c0001t0001g0218 a0001c0001t0001g0219 others(21): Show |
24 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.232+4437G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901052 | |||||||
| chr2:47901058 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0032 others(103): Show |
108 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.232+4431A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901058 | |||||||
| chr2:47901065 | A | G | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.232+4424T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901065 | |||||||
| chr2:47901071 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.232+4418T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901071 | |||||||
| chr2:47901072 | T | TAC | 9 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+4415_232+4416d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901072 | |||||||
| chr2:47901086 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.232+4403G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901086 | |||||||
| chr2:47901094 | T | C | 14 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0225 others(11): Show |
14 | HG00280.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+4395A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901094 | |||||||
| chr2:47901095 | A | G | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4394T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901095 | |||||||
| chr2:47901096 | C | T | 15 | a0001c0001t0001g0122 a0001c0001t0001g0156 a0001c0001t0001g0158 others(12): Show |
15 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.232+4393G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901096 | |||||||
| chr2:47901096 | CAT | C | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01346.hp1 HG02723.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+4391_232+4392d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901096 | |||||||
| chr2:47901100 | TATATGTA others(21): Show |
T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG02615.hp2 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.232+4361_232+4388d others(30): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901100 | |||||||
| chr2:47901103 | A | ATG | 35 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0128 others(32): Show |
36 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.232+4384_232+4385d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901103 | |||||||
| chr2:47901103 | A | G | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4386T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901103 | |||||||
| chr2:47901105 | G | A | 13 | a0001c0001t0001g0122 a0001c0001t0001g0225 a0001c0001t0001g0226 others(10): Show |
13 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.232+4384C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901105 | |||||||
| chr2:47901108 | T | C | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4381A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901108 | |||||||
| chr2:47901109 | A | ACACG | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4379_232+4380i others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901109 | |||||||
| chr2:47901111 | A | G | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4378T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901111 | |||||||
| chr2:47901113 | G | A | 11 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(8): Show |
11 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+4376C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901113 | |||||||
| chr2:47901118 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4371G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901118 | |||||||
| chr2:47901120 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4369G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901120 | |||||||
| chr2:47901121 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4368C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901121 | |||||||
| chr2:47901122 | T | TAC | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4366_232+4367i others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901122 | |||||||
| chr2:47901123 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4366C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901123 | |||||||
| chr2:47901125 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4364C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901125 | |||||||
| chr2:47901128 | C | CATATATA others(7): Show |
7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4360_232+4361i others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | |||||||
| chr2:47901128 | C | CATATATA others(155): Show |
1 | a0001c0001t0001g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.232+4360_232+4361i others(164): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | |||||||
| chr2:47901128 | C | CATATATA others(157): Show |
2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+4360_232+4361i others(166): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | |||||||
| chr2:47901128 | C | CATATATA others(155): Show |
1 | a0001c0001t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.232+4360_232+4361i others(164): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | |||||||
| chr2:47901128 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4361G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901128 | |||||||
| chr2:47901131 | G | GTA | 14 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
14 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+4356_232+4357d others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901131 | |||||||
| chr2:47901147 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.232+4342C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901147 | |||||||
| chr2:47901162 | C | CACACGTG others(33): Show |
1 | a0001c0001t0001g0231 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.232+4326_232+4327i others(42): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901162 | |||||||
| chr2:47901162 | C | CACACGTG others(13): Show |
6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG00280.hp2 HG01081.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+4326_232+4327i others(22): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901162 | |||||||
| chr2:47901164 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4325A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901164 | |||||||
| chr2:47901270 | C | T | 7 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG01346.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+4219G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901270 | |||||||
| chr2:47901316 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+4173A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901316 | |||||||
| chr2:47901534 | T | C | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG02922.hp2 HG03225.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+3955A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901534 | |||||||
| chr2:47901667 | CTCAGT | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+3817_232+3821d others(7): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901667 | |||||||
| chr2:47901720 | A | T | 1 | a0001c0001t0002g0046 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.232+3769T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47901720 | |||||||
| chr2:47902252 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.232+3237A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902252 | |||||||
| chr2:47902273 | C | T | 9 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(6): Show |
9 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+3216G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902273 | |||||||
| chr2:47902333 | G | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0216 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.232+3156C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902333 | |||||||
| chr2:47902403 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232+3086C>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902403 | |||||||
| chr2:47902529 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232+2960A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902529 | |||||||
| chr2:47902725 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.232+2764A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902725 | |||||||
| chr2:47902896 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.232+2593A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902896 | |||||||
| chr2:47902919 | TA | T | 6 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(3): Show |
6 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+2569delT | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47902919 | |||||||
| chr2:47903075 | G | A | 5 | a0001c0001t0003g0121 a0001c0001t0003g0232 a0001c0001t0003g0300 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+2414C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903075 | |||||||
| chr2:47903193 | T | G | 7 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+2296A>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903193 | |||||||
| chr2:47903416 | G | A | 4 | a0001c0001t0003g0232 a0001c0001t0003g0300 a0001c0001t0003g0301 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+2073C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903416 | |||||||
| chr2:47903453 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0002g0289 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.232+2036A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903453 | |||||||
| chr2:47903567 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+1922A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903567 | |||||||
| chr2:47903703 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.232+1786A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903703 | |||||||
| chr2:47903778 | A | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG01358.hp2 HG03017.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+1711T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903778 | |||||||
| chr2:47903782 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.232+1707T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903782 | |||||||
| chr2:47903800 | G | A | 22 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(19): Show |
22 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.232+1689C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903800 | |||||||
| chr2:47903810 | G | C | 23 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(20): Show |
23 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.232+1679C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903810 | |||||||
| chr2:47903825 | G | A | 1 | a0006c0008t0001g0304 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.232+1664C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47903825 | |||||||
| chr2:47904150 | A | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0299 a0001c0001t0002g0033 |
3 | HG02071.hp1 NA18967.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.232+1339T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904150 | |||||||
| chr2:47904176 | T | C | 1 | a0006c0008t0001g0304 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.232+1313A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904176 | |||||||
| chr2:47904184 | C | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(43): Show |
48 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.232+1305G>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904184 | |||||||
| chr2:47904247 | A | C | 6 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 others(3): Show |
6 | HG00738.hp1 HG01109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+1242T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904247 | |||||||
| chr2:47904284 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.232+1205T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904284 | |||||||
| chr2:47904581 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.232+908T>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AAC | A | 20 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0001g0039 others(17): Show |
21 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.232+906_232+907del others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACAC | A | 43 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0068 others(40): Show |
43 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.232+904_232+907del others(4): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACACAC | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0035 others(86): Show |
90 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.232+902_232+907del others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACACACA others(1): Show |
A | 33 | a0001c0001t0001g0077 a0001c0001t0001g0139 a0001c0001t0001g0156 others(30): Show |
33 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.232+900_232+907del others(8): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACACACA others(3): Show |
A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(69): Show |
75 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.232+898_232+907del others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACACACA others(5): Show |
A | 23 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
23 | HG00738.hp1 HG01109.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.232+896_232+907del others(12): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACACACA others(7): Show |
A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0207 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+894_232+907del others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACACACA others(9): Show |
A | 13 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0096 others(10): Show |
13 | HG00280.hp2 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.232+892_232+907del others(16): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACACACA others(11): Show |
A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0226 |
2 | HG01516.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.232+890_232+907del others(18): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904581 | AACACACA others(13): Show |
A | 1 | a0001c0001t0001g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.232+888_232+907del others(20): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904581 | |||||||
| chr2:47904584 | A | G | 1 | a0001c0001t0002g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.232+905T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904584 | |||||||
| chr2:47904587 | C | A | 1 | a0001c0001t0002g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.232+902G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904587 | |||||||
| chr2:47904621 | C | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0030 |
3 | HG01243.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.232+868G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904621 | |||||||
| chr2:47904709 | C | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(206): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.232+780G>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904709 | |||||||
| chr2:47904797 | T | C | 66 | a0001c0001t0001g0006 a0001c0001t0001g0237 a0001c0001t0001g0253 others(63): Show |
68 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.232+692A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904797 | |||||||
| chr2:47904885 | T | A | 1 | a0001c0001t0001g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.232+604A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47904885 | |||||||
| chr2:47905020 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.232+469T>C | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905020 | |||||||
| chr2:47905157 | T | C | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.232+332A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905157 | |||||||
| chr2:47905185 | G | C | 1 | a0001c0001t0001g0296 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.232+304C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905185 | |||||||
| chr2:47905204 | A | T | 1 | a0001c0001t0002g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.232+285T>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905204 | |||||||
| chr2:47905224 | G | C | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.232+265C>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905224 | |||||||
| chr2:47905235 | T | A | 1 | a0001c0002t0002g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.232+254A>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905235 | |||||||
| chr2:47905295 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.232+194C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905295 | |||||||
| chr2:47905349 | G | A | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.232+140C>T | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905349 | |||||||
| chr2:47905355 | C | T | 1 | a0004c0005t0002g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.232+134G>A | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905355 | |||||||
| chr2:47905400 | GCCCCCGC others(9): Show |
G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(11): Show |
14 | HG01433.hp1 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+73_232+88delGG others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905400 | |||||||
| chr2:47905402 | C | CCCCG | 5 | a0001c0002t0002g0197 a0001c0002t0002g0198 a0001c0002t0002g0200 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+83_232+86dupCG others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | |||||||
| chr2:47905402 | CCCCG | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(94): Show |
99 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.232+83_232+86delCG others(2): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | |||||||
| chr2:47905402 | CCCCGCCC others(1): Show |
C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0071 a0001c0001t0001g0225 others(14): Show |
17 | HG00280.hp2 HG00738.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.232+79_232+86delCG others(6): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | |||||||
| chr2:47905402 | CCCCGCCC others(5): Show |
C | 7 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
7 | HG01358.hp2 HG01981.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+75_232+86delCG others(10): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | |||||||
| chr2:47905402 | CCCCGCCC others(9): Show |
C | 2 | a0001c0001t0001g0303 a0001c0001t0002g0150 |
2 | HG02155.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.232+71_232+86delCG others(14): Show |
FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905402 | |||||||
| chr2:47905467 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232+22A>G | FBXO11 | ENSG00000138081.22 | transcript | ENST00000403359.8 | protein_coding | 1/22 | chr2 | 47905467 |