Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51433 |
|---|---|
| ensemblid | ENSG00000089053.13 |
| hgncid | 15713 |
| symbol | ANAPC5 |
| name | anaphase promoting complex subunit 5 |
| refseq_nuc | NM_016237.5 |
| refseq_prot | NP_057321.2 |
| ensembl_nuc | ENST00000261819.8 |
| ensembl_prot | ENSP00000261819.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 121308245 |
| end | 121352411 |
| strand | - |
| ver | v1.2 |
| region | chr12:121308245-121352411 |
| region5000 | chr12:121303245-121357411 |
| regionname0 | ANAPC5_chr12_121308245_121352411 |
| regionname5000 | ANAPC5_chr12_121303245_121357411 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 755 | 277 | 88 | 55 | 98 | 6 | 28 | 64 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0002 | 0/0 | 755 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2268 | 258 | 76 | 53 | 96 | 6 | 25 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| c0002 | 0/0 | 2268 | 10 | 8 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| c0003 | 0/0 | 2268 | 3 | 0 | 0 | 0 | 0 | 3 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| c0004 | 0/0 | 2268 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| c0005 | 0/0 | 2268 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| c0006 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| c0007 | 0/0 | 2268 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| c0008 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 307 | 272 | 83 | 55 | 98 | 6 | 28 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| t0002 | 0/0 | 307 | 5 | 4 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| t0003 | 0/0 | 307 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0014 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2268 | 258 | 76 | 53 | 96 | 6 | 25 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0002 | 0/0 | 2268 | 10 | 8 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0003 | 0/0 | 2268 | 3 | 0 | 0 | 0 | 0 | 3 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0004 | 0/0 | 2268 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0005 | 0/0 | 2268 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0006 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0008 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0002c0007 | 0/0 | 2268 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2574 | 253 | 72 | 52 | 96 | 6 | 25 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0001t0002 | 0/0 | 2574 | 4 | 3 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0001t0003 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0002t0001 | 0/0 | 2574 | 10 | 8 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0003t0001 | 0/0 | 2574 | 3 | 0 | 0 | 0 | 0 | 3 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0004t0001 | 0/0 | 2574 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0005t0001 | 0/0 | 2574 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0006t0001 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0001c0008t0002 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| a0002c0007t0001 | 0/0 | 2574 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | copy fasta | chr12 | 121303245 | 121357411 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0008t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0002c0007t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00741 | hp2 | a0002 | c0007 | t0001 | g0228 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02083 | hp1 | a0001 | c0005 | t0001 | g0053 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02155 | hp1 | a0001 | c0005 | t0001 | g0030 | EAS | CDX | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0095 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0012 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0027 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0085 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0012 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG06807 | hp1 | a0001 | c0008 | t0002 | g0235 | AFR | USA | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0099 | AFR | USA | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | USA | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0134 | REF | REF | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121318281
|
G | A | 1 | a0002 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.1889C>T | p.Ala630Val | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/17 | 1960/2574 | 1889/2268 | 630/755 | chr12 | 121318281 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121308534
|
C | T | 1 | a0001c0003 | 3 | HG02683.hp2 HG03834.hp1 HG04184.hp1 |
synonymous_variant | LOW | c.2214G>A | p.Arg738Arg | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 17/17 | 2285/2574 | 2214/2268 | 738/755 | chr12 | 121308534 | ||
| chr12:121308612
|
G | A | 1 | a0001c0004 | 2 | HG02622.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.2136C>T | p.Asp712Asp | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 17/17 | 2207/2574 | 2136/2268 | 712/755 | chr12 | 121308612 | ||
| chr12:121309714
|
C | T | 1 | a0001c0003 | 3 | HG02683.hp2 HG03834.hp1 HG04184.hp1 |
synonymous_variant | LOW | c.2043G>A | p.Pro681Pro | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/17 | 2114/2574 | 2043/2268 | 681/755 | chr12 | 121309714 | ||
| chr12:121318412
|
G | A | 1 | a0001c0005 | 2 | HG02083.hp1 HG02155.hp1 |
synonymous_variant | LOW | c.1758C>T | p.Ser586Ser | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/17 | 1829/2574 | 1758/2268 | 586/755 | chr12 | 121318412 | ||
| chr12:121320403
|
A | T | 2 | a0001c0002a0001c0004 | 12 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(9): Show |
synonymous_variant | LOW | c.1497T>A | p.Pro499Pro | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 12/17 | 1568/2574 | 1497/2268 | 499/755 | chr12 | 121320403 | ||
| chr12:121327120
|
G | A | 1 | a0001c0008 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1416C>T | p.His472His | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/17 | 1487/2574 | 1416/2268 | 472/755 | chr12 | 121327120 | ||
| chr12:121335685
|
A | G | 1 | a0001c0006 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.798T>C | p.Asp266Asp | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/17 | 869/2574 | 798/2268 | 266/755 | chr12 | 121335685 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121308396
|
A | G | 1 | a0001c0001t0003 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*84T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 17/17 | 84 | chr12 | 121308396 | |||||
| chr12:121352375
|
G | A | 2 | a0001c0001t0002a0001c0008t0002 | 5 | HG01106.hp2 HG02647.hp1 HG02922.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-35C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/17 | 35 | chr12 | 121352375 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121308739
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2057-48C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121308739 | ||||||
| chr12:121309146
|
C | CA | 23 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0038others(20): Show | 25 | HG00438.hp1 HG00558.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.2057-456dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121309146 | ||||||
| chr12:121309146
|
CA | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 86 | HG00558.hp1 HG01109.hp1 HG01123.hp1 others(83): Show |
intron_variant | MODIFIER | c.2057-456delT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121309146 | ||||||
| chr12:121309161
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2057-470T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121309161 | ||||||
| chr12:121309165
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2057-474T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121309165 | ||||||
| chr12:121309188
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(3): Show | 8 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2057-497G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121309188 | ||||||
| chr12:121309313
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2056+388C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121309313 | ||||||
| chr12:121309387
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2056+314C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121309387 | ||||||
| chr12:121309990
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1894-127G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121309990 | ||||||
| chr12:121310252
|
A | AAGAG | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 181 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.1894-393_1894-390d others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310252 | ||||||
| chr12:121310252
|
A | AGAG | 6 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0052others(3): Show | 6 | HG00673.hp1 HG00673.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1894-390_1894-389i others(5): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310252 | ||||||
| chr12:121310453
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1894-590G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310453 | ||||||
| chr12:121310548
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(3): Show | 8 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1894-685C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310548 | ||||||
| chr12:121310602
|
G | A | 7 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(4): Show | 7 | HG01884.hp1 HG02622.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1894-739C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310602 | ||||||
| chr12:121310734
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1894-871C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310734 | ||||||
| chr12:121310761
|
C | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0028others(19): Show | 32 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.1894-898G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310761 | ||||||
| chr12:121310900
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0075others(5): Show | 18 | HG01109.hp1 HG02109.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1894-1037G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310900 | ||||||
| chr12:121310933
|
C | CA | 18 | a0001c0001t0001g0041a0001c0001t0001g0083a0001c0001t0001g0084others(15): Show | 18 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.1894-1071dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310933 | ||||||
| chr12:121310933
|
C | CAA | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 101 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(98): Show |
intron_variant | MODIFIER | c.1894-1072_1894-107 others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310933 | ||||||
| chr12:121310933
|
C | CAAA | 14 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0071others(11): Show | 16 | HG01243.hp2 HG01891.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.1894-1073_1894-107 others(7): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121310933 | ||||||
| chr12:121311029
|
CT | C | 13 | a0001c0001t0001g0024a0001c0001t0001g0062a0001c0001t0001g0063others(10): Show | 13 | HG01099.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1894-1167delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311029 | ||||||
| chr12:121311040
|
T | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0193others(2): Show | 7 | HG00438.hp1 HG02071.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1894-1177A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311040 | ||||||
| chr12:121311268
|
T | A | 2 | a0001c0003t0001g0012a0001c0003t0001g0085 | 3 | HG02683.hp2 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1894-1405A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311268 | ||||||
| chr12:121311441
|
C | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0146 | 3 | HG03490.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1894-1578G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311441 | ||||||
| chr12:121311489
|
CA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 110 | HG00558.hp1 HG01099.hp1 HG01109.hp1 others(107): Show |
intron_variant | MODIFIER | c.1894-1627delT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311489 | ||||||
| chr12:121311496
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 110 | HG00558.hp1 HG01099.hp1 HG01109.hp1 others(107): Show |
intron_variant | MODIFIER | c.1894-1633A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311496 | ||||||
| chr12:121311549
|
T | C | 1 | a0001c0001t0001g0134 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1894-1686A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311549 | ||||||
| chr12:121311758
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 123 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(120): Show |
intron_variant | MODIFIER | c.1894-1895T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311758 | ||||||
| chr12:121311852
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1894-1989T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121311852 | ||||||
| chr12:121312263
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG01884.hp2 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1894-2400A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121312263 | ||||||
| chr12:121312285
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0201 | 3 | HG00140.hp1 HG01192.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1894-2422A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121312285 | ||||||
| chr12:121312334
|
C | G | 11 | a0001c0001t0001g0024a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01099.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1894-2471G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121312334 | ||||||
| chr12:121312546
|
C | CA | 9 | a0001c0001t0001g0024a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 9 | HG01099.hp1 HG01884.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1894-2684dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121312546 | ||||||
| chr12:121312706
|
C | CA | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 128 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1894-2844dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121312706 | ||||||
| chr12:121312706
|
C | CAA | 33 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0044others(30): Show | 34 | HG00558.hp1 HG01099.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1894-2845_1894-284 others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121312706 | ||||||
| chr12:121312879
|
C | CA | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0028others(19): Show | 32 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.1894-3017dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121312879 | ||||||
| chr12:121313012
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-3149C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121313012 | ||||||
| chr12:121313186
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0028others(19): Show | 32 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.1894-3323G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121313186 | ||||||
| chr12:121313301
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1894-3438G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121313301 | ||||||
| chr12:121313310
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1894-3447C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121313310 | ||||||
| chr12:121313791
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0071a0001c0001t0001g0072others(3): Show | 7 | NA18945.hp1 NA18955.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1894-3928C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121313791 | ||||||
| chr12:121314247
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1893+4030T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121314247 | ||||||
| chr12:121314620
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0066 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1893+3657A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121314620 | ||||||
| chr12:121314624
|
C | CT | 38 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(35): Show | 43 | HG00558.hp1 HG01243.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1893+3652dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121314624 | ||||||
| chr12:121314863
|
T | A | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1893+3414A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121314863 | ||||||
| chr12:121314958
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0054 | 2 | HG02135.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1893+3319A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121314958 | ||||||
| chr12:121315274
|
T | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1893+3003A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121315274 | ||||||
| chr12:121315465
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1893+2812C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121315465 | ||||||
| chr12:121315500
|
A | AAAG | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 123 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(120): Show |
intron_variant | MODIFIER | c.1893+2774_1893+277 others(7): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121315500 | ||||||
| chr12:121315745
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1893+2532G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121315745 | ||||||
| chr12:121315752
|
A | T | 2 | a0001c0003t0001g0012a0001c0003t0001g0085 | 3 | HG02683.hp2 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1893+2525T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121315752 | ||||||
| chr12:121315910
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 124 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(121): Show |
intron_variant | MODIFIER | c.1893+2367A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121315910 | ||||||
| chr12:121315998
|
A | G | 3 | a0001c0001t0001g0189a0001c0001t0001g0211a0001c0001t0001g0223 | 3 | HG02083.hp2 HG02155.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1893+2279T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121315998 | ||||||
| chr12:121316018
|
G | T | 1 | a0001c0001t0001g0188 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1893+2259C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316018 | ||||||
| chr12:121316088
|
T | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1893+2189A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316088 | ||||||
| chr12:121316419
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1893+1858C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316419 | ||||||
| chr12:121316452
|
C | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 110 | HG00558.hp1 HG01099.hp1 HG01109.hp1 others(107): Show |
intron_variant | MODIFIER | c.1893+1825G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316452 | ||||||
| chr12:121316608
|
C | T | 6 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1893+1669G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316608 | ||||||
| chr12:121316686
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1893+1591A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316686 | ||||||
| chr12:121316723
|
ACT | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1893+1552_1893+155 others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316723 | ||||||
| chr12:121316732
|
C | CA | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 73 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.1893+1544dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316732 | ||||||
| chr12:121316732
|
C | CAA | 9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0062others(6): Show | 9 | HG01891.hp2 HG02630.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1893+1543_1893+154 others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316732 | ||||||
| chr12:121316732
|
CA | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0071others(18): Show | 22 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1893+1544delT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316732 | ||||||
| chr12:121316732
|
CAA | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(16): Show | 24 | HG01243.hp2 HG01346.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1893+1543_1893+154 others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316732 | ||||||
| chr12:121316768
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 110 | HG00558.hp1 HG01099.hp1 HG01109.hp1 others(107): Show |
intron_variant | MODIFIER | c.1893+1509C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316768 | ||||||
| chr12:121316914
|
C | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 275 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(272): Show |
intron_variant | MODIFIER | c.1893+1363G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316914 | ||||||
| chr12:121317253
|
CT | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0081others(13): Show | 17 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1893+1023delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317253 | ||||||
| chr12:121317323
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG01884.hp2 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1893+954C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317323 | ||||||
| chr12:121317411
|
GC | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02258.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1893+865delG | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317411 | ||||||
| chr12:121317414
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1893+863G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317414 | ||||||
| chr12:121317473
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 277 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.1893+804A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317473 | ||||||
| chr12:121317549
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1893+728C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317549 | ||||||
| chr12:121317644
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1893+633G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317644 | ||||||
| chr12:121317671
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1893+606G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317671 | ||||||
| chr12:121317718
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(3): Show | 8 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1893+559A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317718 | ||||||
| chr12:121317758
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 123 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(120): Show |
intron_variant | MODIFIER | c.1893+519T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317758 | ||||||
| chr12:121317927
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1893+350T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317927 | ||||||
| chr12:121318164
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02258.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1893+113G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121318164 | ||||||
| chr12:121318431
|
G | A | 2 | a0001c0001t0001g0140a0001c0008t0002g0235 | 2 | HG06807.hp1 NA19002.hp2 |
splice_region_variant&intron_variant | LOW | c.1746-7C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 14/16 | chr12 | 121318431 | ||||||
| chr12:121318747
|
G | A | 46 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(43): Show | 52 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(49): Show |
intron_variant | MODIFIER | c.1638-139C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121318747 | ||||||
| chr12:121318806
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1638-198C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121318806 | ||||||
| chr12:121318839
|
G | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 123 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(120): Show |
intron_variant | MODIFIER | c.1638-231C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121318839 | ||||||
| chr12:121318881
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1638-273C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121318881 | ||||||
| chr12:121319005
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1638-397C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319005 | ||||||
| chr12:121319019
|
C | CA | 6 | a0001c0001t0001g0106a0001c0001t0001g0197a0001c0001t0001g0200others(3): Show | 6 | HG02738.hp1 HG03098.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-412dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319019 | ||||||
| chr12:121319108
|
T | TAC | 11 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0083others(8): Show | 13 | HG01243.hp1 HG02683.hp2 HG02897.hp2 others(10): Show |
intron_variant | MODIFIER | c.1638-502_1638-501d others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319108 | ||||||
| chr12:121319108
|
TACACAA | T | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0135others(3): Show | 6 | HG01074.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-506_1638-501d others(8): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319108 | ||||||
| chr12:121319110
|
CACAA | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0087others(25): Show | 29 | HG01069.hp1 HG01099.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1638-506_1638-503d others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319110 | ||||||
| chr12:121319112
|
CAA | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(35): Show | 48 | HG00558.hp1 HG01099.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1638-506_1638-505d others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319112 | ||||||
| chr12:121319114
|
A | C | 35 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(32): Show | 41 | HG01243.hp1 HG01243.hp2 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.1638-506T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319114 | ||||||
| chr12:121319114
|
AAC | A | 29 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(26): Show | 32 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1638-508_1638-507d others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319114 | ||||||
| chr12:121319114
|
AACAC | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0219 | 3 | HG00621.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1638-510_1638-507d others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319114 | ||||||
| chr12:121319237
|
CT | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 116 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(113): Show |
intron_variant | MODIFIER | c.1637+459delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319237 | ||||||
| chr12:121319297
|
A | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02258.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1637+400T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319297 | ||||||
| chr12:121319407
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1637+290A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319407 | ||||||
| chr12:121319499
|
GCTGGGAT others(3): Show |
G | 1 | a0001c0001t0001g0199 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1637+188_1637+197d others(12): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319499 | ||||||
| chr12:121319505
|
ATTACAGG others(19): Show |
A | 2 | a0001c0001t0001g0103a0001c0001t0001g0198 | 2 | HG01517.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1637+166_1637+191d others(28): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319505 | ||||||
| chr12:121319508
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1637+189T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319508 | ||||||
| chr12:121319510
|
A | T | 1 | a0001c0001t0001g0199 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1637+187T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319510 | ||||||
| chr12:121319512
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1637+185C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319512 | ||||||
| chr12:121319518
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1637+179C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319518 | ||||||
| chr12:121319530
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0199 | 2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1637+167T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319530 | ||||||
| chr12:121319531
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0199 | 2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1637+166C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319531 | ||||||
| chr12:121319857
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 124 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(121): Show |
intron_variant | MODIFIER | c.1516-39C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 12/16 | chr12 | 121319857 | ||||||
| chr12:121319954
|
T | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 123 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(120): Show |
intron_variant | MODIFIER | c.1516-136A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 12/16 | chr12 | 121319954 | ||||||
| chr12:121320159
|
G | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0129 | 2 | NA19007.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1515+226C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 12/16 | chr12 | 121320159 | ||||||
| chr12:121320159
|
G | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 122 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(119): Show |
intron_variant | MODIFIER | c.1515+226C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 12/16 | chr12 | 121320159 | ||||||
| chr12:121320228
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1515+157T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 12/16 | chr12 | 121320228 | ||||||
| chr12:121320309
|
T | C | 2 | a0001c0001t0002g0236a0001c0001t0002g0239 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1515+76A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 12/16 | chr12 | 121320309 | ||||||
| chr12:121320479
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1441-20A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320479 | ||||||
| chr12:121320559
|
G | C | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0141others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-100C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320559 | ||||||
| chr12:121320621
|
T | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0201 | 3 | HG00140.hp1 HG01192.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1441-162A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320621 | ||||||
| chr12:121320662
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1441-203C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320662 | ||||||
| chr12:121320666
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1441-207C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320666 | ||||||
| chr12:121320688
|
C | T | 27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(24): Show | 30 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1441-229G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320688 | ||||||
| chr12:121320691
|
T | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-232A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320691 | ||||||
| chr12:121320695
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-236G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320695 | ||||||
| chr12:121320710
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG01884.hp2 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1441-251G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320710 | ||||||
| chr12:121320752
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG01884.hp2 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1441-293C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320752 | ||||||
| chr12:121320810
|
A | C | 11 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1441-351T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320810 | ||||||
| chr12:121320860
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0239 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1441-401G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320860 | ||||||
| chr12:121320902
|
CAG | C | 43 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(40): Show | 48 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.1441-445_1441-444d others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121320902 | ||||||
| chr12:121321015
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1441-556G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321015 | ||||||
| chr12:121321047
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(37): Show | 50 | HG01099.hp1 HG01109.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.1441-588G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321047 | ||||||
| chr12:121321164
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-705C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321164 | ||||||
| chr12:121321245
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-786C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321245 | ||||||
| chr12:121321260
|
AT | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-802delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321260 | ||||||
| chr12:121321261
|
T | A | 7 | a0001c0001t0001g0074a0001c0001t0001g0084a0001c0001t0001g0131others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-802A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321261 | ||||||
| chr12:121321269
|
T | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG01123.hp1 HG02148.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-810A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321269 | ||||||
| chr12:121321343
|
C | CT | 57 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(54): Show | 64 | HG00558.hp1 HG01099.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.1441-885dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321343 | ||||||
| chr12:121321343
|
C | CTT | 8 | a0001c0001t0001g0072a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG01074.hp1 HG01346.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1441-886_1441-885d others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321343 | ||||||
| chr12:121321343
|
CT | C | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 42 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1441-885delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321343 | ||||||
| chr12:121321513
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG01517.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1441-1054G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321513 | ||||||
| chr12:121321532
|
C | CT | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 101 | HG00558.hp1 HG01099.hp1 HG01109.hp1 others(98): Show |
intron_variant | MODIFIER | c.1441-1074dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321532 | ||||||
| chr12:121321685
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1441-1226C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321685 | ||||||
| chr12:121321752
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1441-1293C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321752 | ||||||
| chr12:121321853
|
G | A | 43 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(40): Show | 48 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.1441-1394C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321853 | ||||||
| chr12:121321872
|
C | CT | 12 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(9): Show | 12 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1441-1414dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321872 | ||||||
| chr12:121321953
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1441-1494G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321953 | ||||||
| chr12:121322048
|
G | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 111 | HG00558.hp1 HG01099.hp1 HG01109.hp1 others(108): Show |
intron_variant | MODIFIER | c.1441-1589C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322048 | ||||||
| chr12:121322115
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1441-1656G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322115 | ||||||
| chr12:121322165
|
G | GT | 20 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0131others(17): Show | 21 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1441-1707dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322165 | ||||||
| chr12:121322379
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0171a0001c0001t0001g0184others(1): Show | 4 | HG00609.hp1 NA18950.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-1920G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322379 | ||||||
| chr12:121322585
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0225 | 2 | HG02258.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1441-2126G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322585 | ||||||
| chr12:121322586
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-2127C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322586 | ||||||
| chr12:121322647
|
ATT | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1441-2190_1441-218 others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322647 | ||||||
| chr12:121322671
|
A | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(41): Show | 49 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.1441-2212T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322671 | ||||||
| chr12:121322848
|
C | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(24): Show | 32 | HG00558.hp1 HG01243.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1441-2389G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322848 | ||||||
| chr12:121322893
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | NA18945.hp1 NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1441-2434G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322893 | ||||||
| chr12:121322993
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1441-2534G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322993 | ||||||
| chr12:121323054
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0055others(7): Show | 20 | HG01109.hp1 HG02109.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1441-2595T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121323054 | ||||||
| chr12:121323217
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1441-2758A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121323217 | ||||||
| chr12:121323260
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1441-2801C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121323260 | ||||||
| chr12:121323315
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1441-2856T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121323315 | ||||||
| chr12:121323320
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1441-2861G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121323320 | ||||||
| chr12:121323718
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1441-3259G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121323718 | ||||||
| chr12:121323729
|
CAT | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0146 | 4 | HG03490.hp2 HG03492.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-3272_1441-327 others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121323729 | ||||||
| chr12:121323973
|
G | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(37): Show | 50 | HG01099.hp1 HG01109.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.1440+3123C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121323973 | ||||||
| chr12:121324124
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0008t0002g0235 | 3 | HG02109.hp2 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1440+2972G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121324124 | ||||||
| chr12:121324192
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1440+2904C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121324192 | ||||||
| chr12:121324327
|
G | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1440+2769C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121324327 | ||||||
| chr12:121324393
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1440+2703A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121324393 | ||||||
| chr12:121324808
|
G | A | 2 | a0001c0003t0001g0012a0001c0003t0001g0085 | 3 | HG02683.hp2 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1440+2288C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121324808 | ||||||
| chr12:121324811
|
G | GTT | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02258.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1440+2283_1440+228 others(6): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121324811 | ||||||
| chr12:121324845
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1440+2251C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121324845 | ||||||
| chr12:121325179
|
C | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(195): Show | 227 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.1440+1917G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325179 | ||||||
| chr12:121325190
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1440+1906G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325190 | ||||||
| chr12:121325441
|
TGACA | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(3): Show | 8 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1440+1651_1440+165 others(8): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325441 | ||||||
| chr12:121325505
|
TTAAAAA | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0209 | 3 | NA18952.hp2 NA18962.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1440+1585_1440+159 others(10): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325505 | ||||||
| chr12:121325506
|
T | TA | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 119 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(116): Show |
intron_variant | MODIFIER | c.1440+1589dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325506 | ||||||
| chr12:121325511
|
A | AT | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(124): Show | 149 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.1440+1584_1440+158 others(5): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325511 | ||||||
| chr12:121325702
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1440+1394T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325702 | ||||||
| chr12:121325810
|
T | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(41): Show | 49 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.1440+1286A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325810 | ||||||
| chr12:121325978
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0130others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+1118G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325978 | ||||||
| chr12:121326067
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(195): Show | 227 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.1440+1029T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121326067 | ||||||
| chr12:121326102
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1440+994T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121326102 | ||||||
| chr12:121326361
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 121 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1440+735A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121326361 | ||||||
| chr12:121326996
|
A | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(196): Show | 228 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(225): Show |
intron_variant | MODIFIER | c.1440+100T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121326996 | ||||||
| chr12:121327297
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1305-66C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 10/16 | chr12 | 121327297 | ||||||
| chr12:121327441
|
C | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02258.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1305-210G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 10/16 | chr12 | 121327441 | ||||||
| chr12:121327472
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1305-241C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 10/16 | chr12 | 121327472 | ||||||
| chr12:121327488
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1305-257C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 10/16 | chr12 | 121327488 | ||||||
| chr12:121327755
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1305-524G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 10/16 | chr12 | 121327755 | ||||||
| chr12:121327797
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1304+519T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 10/16 | chr12 | 121327797 | ||||||
| chr12:121327952
|
C | A | 12 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(9): Show | 12 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1304+364G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 10/16 | chr12 | 121327952 | ||||||
| chr12:121328065
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1304+251A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 10/16 | chr12 | 121328065 | ||||||
| chr12:121328716
|
C | T | 11 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1123-219G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121328716 | ||||||
| chr12:121329080
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1123-583T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329080 | ||||||
| chr12:121329192
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1123-695G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329192 | ||||||
| chr12:121329315
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1123-818C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329315 | ||||||
| chr12:121329465
|
A | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(21): Show | 29 | HG00558.hp1 HG01243.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.1123-968T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329465 | ||||||
| chr12:121329617
|
C | CT | 7 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG01069.hp2 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+965dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329617 | ||||||
| chr12:121329617
|
CT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(23): Show | 34 | HG00438.hp2 HG00673.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.1122+965delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329617 | ||||||
| chr12:121329656
|
C | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(206): Show | 238 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1122+927G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329656 | ||||||
| chr12:121329687
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1122+896G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329687 | ||||||
| chr12:121329756
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1122+827G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329756 | ||||||
| chr12:121329814
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1122+769G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121329814 | ||||||
| chr12:121330408
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02148.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1122+175G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121330408 | ||||||
| chr12:121330445
|
C | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(124): Show | 149 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.1122+138G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121330445 | ||||||
| chr12:121330541
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1122+42G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 9/16 | chr12 | 121330541 | ||||||
| chr12:121330680
|
G | C | 1 | a0001c0001t0001g0207 | 1 | NA18979.hp2 | splice_region_variant&intron_variant | LOW | c.1033-8C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 8/16 | chr12 | 121330680 | ||||||
| chr12:121331454
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.951-26G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121331454 | ||||||
| chr12:121331462
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG01517.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.951-34A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121331462 | ||||||
| chr12:121331505
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.951-77A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121331505 | ||||||
| chr12:121331838
|
ATGTT | A | 10 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0133others(7): Show | 10 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.951-414_951-411del others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121331838 | ||||||
| chr12:121331852
|
G | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.951-424C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121331852 | ||||||
| chr12:121331900
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.951-472C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121331900 | ||||||
| chr12:121331926
|
TGAATTCC others(8): Show |
T | 1 | a0001c0001t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.951-513_951-499del others(15): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121331926 | ||||||
| chr12:121331945
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.951-517C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121331945 | ||||||
| chr12:121332101
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(22): Show | 33 | HG00438.hp2 HG00673.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.951-673G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332101 | ||||||
| chr12:121332201
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.951-773C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332201 | ||||||
| chr12:121332208
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.951-780G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332208 | ||||||
| chr12:121332343
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.951-915A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332343 | ||||||
| chr12:121332518
|
T | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 174 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.951-1090A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332518 | ||||||
| chr12:121332577
|
G | GT | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 221 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.951-1150dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332577 | ||||||
| chr12:121332621
|
T | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(54): Show | 64 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.951-1193A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332621 | ||||||
| chr12:121332724
|
C | T | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0141others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.951-1296G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332724 | ||||||
| chr12:121332942
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.951-1514C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332942 | ||||||
| chr12:121332967
|
G | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0201 | 3 | HG00140.hp1 HG01192.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.951-1539C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332967 | ||||||
| chr12:121332996
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.951-1568A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332996 | ||||||
| chr12:121333129
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.951-1701C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333129 | ||||||
| chr12:121333137
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.951-1709C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333137 | ||||||
| chr12:121333144
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.951-1716G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333144 | ||||||
| chr12:121333411
|
C | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(3): Show | 8 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.951-1983G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333411 | ||||||
| chr12:121333492
|
C | A | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG02258.hp2 HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.950+2041G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333492 | ||||||
| chr12:121333492
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.950+2041G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333492 | ||||||
| chr12:121333544
|
T | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG01891.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.950+1989A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333544 | ||||||
| chr12:121333770
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950+1763G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333770 | ||||||
| chr12:121333829
|
T | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(27): Show | 35 | HG00558.hp1 HG00558.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.950+1704A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333829 | ||||||
| chr12:121333972
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.950+1561A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121333972 | ||||||
| chr12:121334127
|
A | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0038others(9): Show | 13 | HG00609.hp1 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.950+1406T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334127 | ||||||
| chr12:121334176
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.950+1357C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334176 | ||||||
| chr12:121334219
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(18): Show | 26 | HG00558.hp1 HG01346.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.950+1314G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334219 | ||||||
| chr12:121334479
|
G | C | 1 | a0001c0008t0002g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.950+1054C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334479 | ||||||
| chr12:121334507
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.950+1026T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334507 | ||||||
| chr12:121334568
|
T | C | 10 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0002t0001g0094others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.950+965A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334568 | ||||||
| chr12:121334654
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.950+879T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334654 | ||||||
| chr12:121334727
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.950+806G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334727 | ||||||
| chr12:121334986
|
TC | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(33): Show | 41 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.950+546delG | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334986 | ||||||
| chr12:121335063
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950+470T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121335063 | ||||||
| chr12:121335078
|
T | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.950+455A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121335078 | ||||||
| chr12:121335166
|
A | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.950+367T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121335166 | ||||||
| chr12:121335227
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | NA18945.hp1 NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.950+306C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121335227 | ||||||
| chr12:121335413
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0100 | 2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.950+120C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121335413 | ||||||
| chr12:121335476
|
C | A | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.950+57G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121335476 | ||||||
| chr12:121335749
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(128): Show | 153 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.760-26A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121335749 | ||||||
| chr12:121335790
|
G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(3): Show | 8 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.760-67C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121335790 | ||||||
| chr12:121335848
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.760-125C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121335848 | ||||||
| chr12:121336015
|
T | G | 13 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0083others(10): Show | 14 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.760-292A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121336015 | ||||||
| chr12:121336218
|
T | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | NA18946.hp2 NA18979.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.760-495A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121336218 | ||||||
| chr12:121336443
|
C | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(186): Show | 218 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.760-720G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121336443 | ||||||
| chr12:121336471
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.760-748T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121336471 | ||||||
| chr12:121336572
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.759+719C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121336572 | ||||||
| chr12:121336666
|
G | T | 1 | a0001c0001t0002g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.759+625C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121336666 | ||||||
| chr12:121336694
|
C | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(9): Show | 19 | HG00438.hp2 HG00673.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.759+597G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121336694 | ||||||
| chr12:121336709
|
G | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+582C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121336709 | ||||||
| chr12:121337208
|
C | T | 1 | a0001c0006t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.759+83G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121337208 | ||||||
| chr12:121337209
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.759+82A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121337209 | ||||||
| chr12:121337218
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.759+73T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 6/16 | chr12 | 121337218 | ||||||
| chr12:121337408
|
G | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(24): Show | 32 | HG00558.hp1 HG01243.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.658-16C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121337408 | ||||||
| chr12:121337581
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.658-189G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121337581 | ||||||
| chr12:121337653
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.658-261G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121337653 | ||||||
| chr12:121337693
|
T | C | 6 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-301A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121337693 | ||||||
| chr12:121337791
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.658-399G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121337791 | ||||||
| chr12:121337939
|
A | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0105a0001c0001t0001g0107 | 4 | NA18955.hp1 NA18975.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-547T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121337939 | ||||||
| chr12:121338017
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.658-625G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338017 | ||||||
| chr12:121338130
|
T | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(41): Show | 50 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(47): Show |
intron_variant | MODIFIER | c.658-738A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338130 | ||||||
| chr12:121338160
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.658-768C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338160 | ||||||
| chr12:121338244
|
A | T | 6 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-852T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338244 | ||||||
| chr12:121338362
|
G | A | 5 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(2): Show | 5 | HG01884.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.658-970C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338362 | ||||||
| chr12:121338370
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0003t0001g0012others(1): Show | 5 | HG02074.hp2 HG02683.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.658-978T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338370 | ||||||
| chr12:121338512
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.658-1120A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338512 | ||||||
| chr12:121338654
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.658-1262A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338654 | ||||||
| chr12:121338662
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.658-1270T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338662 | ||||||
| chr12:121338739
|
G | GTATATTA others(7): Show |
3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG02258.hp2 HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.658-1348_658-1347i others(16): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338739 | ||||||
| chr12:121338945
|
A | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0177a0001c0001t0001g0210 | 3 | HG01192.hp1 HG03710.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.658-1553T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338945 | ||||||
| chr12:121339054
|
C | CT | 8 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0071others(5): Show | 8 | HG00438.hp2 HG02109.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-1663dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339054 | ||||||
| chr12:121339054
|
CT | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0131others(14): Show | 18 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.658-1663delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339054 | ||||||
| chr12:121339055
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.658-1663A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339055 | ||||||
| chr12:121339312
|
A | C | 10 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0002t0001g0094others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.658-1920T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339312 | ||||||
| chr12:121339362
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.658-1970A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339362 | ||||||
| chr12:121339513
|
CA | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(39): Show | 48 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.658-2122delT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339513 | ||||||
| chr12:121339560
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.658-2168A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339560 | ||||||
| chr12:121339619
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.658-2227A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339619 | ||||||
| chr12:121339657
|
C | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.658-2265G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339657 | ||||||
| chr12:121339749
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(188): Show | 220 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.657+2254T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339749 | ||||||
| chr12:121339761
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.657+2242C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339761 | ||||||
| chr12:121339763
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.657+2240G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339763 | ||||||
| chr12:121339806
|
T | G | 1 | a0001c0001t0001g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.657+2197A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339806 | ||||||
| chr12:121339868
|
G | GT | 67 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(64): Show | 79 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.657+2134dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339868 | ||||||
| chr12:121339868
|
G | GTT | 10 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0067others(7): Show | 10 | HG01099.hp2 HG01243.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+2133_657+2134d others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339868 | ||||||
| chr12:121339868
|
GTTTTTTT others(2): Show |
G | 39 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(36): Show | 44 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.657+2126_657+2134d others(11): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339868 | ||||||
| chr12:121339872
|
T | TG | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG01891.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.657+2130_657+2131i others(3): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339872 | ||||||
| chr12:121339891
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.657+2112A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339891 | ||||||
| chr12:121339914
|
T | C | 2 | a0001c0003t0001g0012a0001c0003t0001g0085 | 3 | HG02683.hp2 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.657+2089A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339914 | ||||||
| chr12:121339929
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.657+2074A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339929 | ||||||
| chr12:121339940
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(25): Show | 33 | HG00558.hp1 HG01243.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.657+2063C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339940 | ||||||
| chr12:121339946
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.657+2057C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339946 | ||||||
| chr12:121340041
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 201 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.657+1962C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340041 | ||||||
| chr12:121340181
|
G | A | 8 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0067others(5): Show | 8 | HG01358.hp2 HG02647.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.657+1822C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340181 | ||||||
| chr12:121340243
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.657+1760C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340243 | ||||||
| chr12:121340316
|
C | CA | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(42): Show | 53 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.657+1686dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340316 | ||||||
| chr12:121340445
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.657+1558C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340445 | ||||||
| chr12:121340519
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.657+1484C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340519 | ||||||
| chr12:121340537
|
A | AT | 11 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.657+1465dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340537 | ||||||
| chr12:121340537
|
AT | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(23): Show | 34 | HG00438.hp2 HG00673.hp2 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.657+1465delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340537 | ||||||
| chr12:121340629
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.657+1374G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340629 | ||||||
| chr12:121340637
|
C | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.657+1366G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340637 | ||||||
| chr12:121340656
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.657+1347C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340656 | ||||||
| chr12:121340678
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.657+1325C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340678 | ||||||
| chr12:121340700
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.657+1303C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340700 | ||||||
| chr12:121340733
|
G | GT | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(124): Show | 149 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.657+1269dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340733 | ||||||
| chr12:121340997
|
T | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0133a0001c0001t0001g0134others(8): Show | 12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.657+1006A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340997 | ||||||
| chr12:121341102
|
T | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(204): Show | 236 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.657+901A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341102 | ||||||
| chr12:121341198
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(25): Show | 33 | HG00558.hp1 HG01243.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.657+805C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341198 | ||||||
| chr12:121341588
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.657+415C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341588 | ||||||
| chr12:121341625
|
A | C | 5 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(2): Show | 5 | HG01884.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+378T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341625 | ||||||
| chr12:121341848
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.657+155G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341848 | ||||||
| chr12:121341857
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+146C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341857 | ||||||
| chr12:121341898
|
A | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034 | 3 | HG01123.hp1 HG02148.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.657+105T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341898 | ||||||
| chr12:121341930
|
A | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0083others(15): Show | 19 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.657+73T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341930 | ||||||
| chr12:121342157
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.591-88C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342157 | ||||||
| chr12:121342196
|
G | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG01891.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.591-127C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342196 | ||||||
| chr12:121342273
|
G | C | 2 | a0001c0003t0001g0012a0001c0003t0001g0085 | 3 | HG02683.hp2 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.591-204C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342273 | ||||||
| chr12:121342284
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591-215G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342284 | ||||||
| chr12:121342472
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.591-403T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342472 | ||||||
| chr12:121342495
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.591-426A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342495 | ||||||
| chr12:121342662
|
C | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | NA18952.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.591-593G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342662 | ||||||
| chr12:121342790
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.591-721A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342790 | ||||||
| chr12:121342808
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0133others(9): Show | 13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.591-739T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342808 | ||||||
| chr12:121342816
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.591-747C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342816 | ||||||
| chr12:121342979
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.591-910T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342979 | ||||||
| chr12:121343167
|
A | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.591-1098T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121343167 | ||||||
| chr12:121343210
|
A | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(46): Show | 61 | HG00140.hp2 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.591-1141T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121343210 | ||||||
| chr12:121343267
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG01884.hp2 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.591-1198T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121343267 | ||||||
| chr12:121343389
|
T | C | 3 | a0001c0001t0001g0093a0001c0003t0001g0012a0001c0003t0001g0085 | 4 | HG02055.hp2 HG02683.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.591-1320A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121343389 | ||||||
| chr12:121343722
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.591-1653A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121343722 | ||||||
| chr12:121343866
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.591-1797A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121343866 | ||||||
| chr12:121343998
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.590+1841C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121343998 | ||||||
| chr12:121343999
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.590+1840C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121343999 | ||||||
| chr12:121344184
|
A | G | 8 | a0001c0001t0001g0035a0001c0002t0001g0094a0001c0002t0001g0096others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.590+1655T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344184 | ||||||
| chr12:121344306
|
C | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0038others(9): Show | 13 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.590+1533G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344306 | ||||||
| chr12:121344317
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.590+1522C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344317 | ||||||
| chr12:121344388
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0140 | 4 | HG01243.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.590+1451C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344388 | ||||||
| chr12:121344388
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590+1451C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344388 | ||||||
| chr12:121344576
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | HG01346.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.590+1263C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344576 | ||||||
| chr12:121344581
|
C | CA | 13 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.590+1257dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344581 | ||||||
| chr12:121344594
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02109.hp2 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.590+1245T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344594 | ||||||
| chr12:121344626
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.590+1213G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344626 | ||||||
| chr12:121344905
|
G | C | 6 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.590+934C>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344905 | ||||||
| chr12:121344910
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590+929T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344910 | ||||||
| chr12:121344980
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.590+859A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121344980 | ||||||
| chr12:121345150
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0075others(5): Show | 18 | HG01109.hp1 HG02109.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.590+689C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121345150 | ||||||
| chr12:121345358
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.590+481A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121345358 | ||||||
| chr12:121345418
|
A | C | 10 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(7): Show | 10 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.590+421T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121345418 | ||||||
| chr12:121346171
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.398-140G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 3/16 | chr12 | 121346171 | ||||||
| chr12:121346296
|
T | A | 1 | a0001c0001t0001g0227 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.398-265A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 3/16 | chr12 | 121346296 | ||||||
| chr12:121346364
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.398-333C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 3/16 | chr12 | 121346364 | ||||||
| chr12:121346390
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.398-359G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 3/16 | chr12 | 121346390 | ||||||
| chr12:121346431
|
G | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | HG01891.hp2 HG02015.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-400C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 3/16 | chr12 | 121346431 | ||||||
| chr12:121346583
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.397+313C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 3/16 | chr12 | 121346583 | ||||||
| chr12:121347094
|
A | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0002t0001g0144 | 3 | HG03209.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.288-89T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 2/16 | chr12 | 121347094 | ||||||
| chr12:121347288
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.288-283C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 2/16 | chr12 | 121347288 | ||||||
| chr12:121347373
|
T | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0002t0001g0144 | 3 | HG03209.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.288-368A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 2/16 | chr12 | 121347373 | ||||||
| chr12:121347522
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.287+280A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 2/16 | chr12 | 121347522 | ||||||
| chr12:121347678
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287+124G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 2/16 | chr12 | 121347678 | ||||||
| chr12:121347992
|
C | A | 107 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 123 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.208-111G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121347992 | ||||||
| chr12:121348046
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.208-165A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348046 | ||||||
| chr12:121348308
|
C | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0219a0001c0001t0001g0220 | 4 | HG00621.hp1 HG02132.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-427G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348308 | ||||||
| chr12:121348370
|
G | A | 10 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(7): Show | 10 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-489C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348370 | ||||||
| chr12:121348549
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 6 | HG01123.hp1 HG02148.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-668G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348549 | ||||||
| chr12:121348659
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00735.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.208-778G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348659 | ||||||
| chr12:121348669
|
A | T | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(96): Show | 113 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.208-788T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348669 | ||||||
| chr12:121348670
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.208-789T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348670 | ||||||
| chr12:121348684
|
C | T | 6 | a0001c0002t0001g0094a0001c0002t0001g0096a0001c0002t0001g0097others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-803G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348684 | ||||||
| chr12:121348936
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0162a0001c0001t0001g0163 | 4 | HG00639.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1055G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348936 | ||||||
| chr12:121348980
|
T | C | 144 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(141): Show | 159 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.208-1099A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348980 | ||||||
| chr12:121348999
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.208-1118A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348999 | ||||||
| chr12:121348999
|
T | G | 16 | a0001c0001t0001g0084a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 17 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.208-1118A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121348999 | ||||||
| chr12:121349002
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.208-1121G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349002 | ||||||
| chr12:121349018
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.208-1137C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349018 | ||||||
| chr12:121349039
|
C | T | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(96): Show | 113 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.208-1158G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349039 | ||||||
| chr12:121349040
|
A | G | 116 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(113): Show | 131 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.208-1159T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349040 | ||||||
| chr12:121349165
|
A | C | 181 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 201 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.208-1284T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349165 | ||||||
| chr12:121349273
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(5): Show | 10 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-1392C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349273 | ||||||
| chr12:121349324
|
G | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0161 | 2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.208-1443C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349324 | ||||||
| chr12:121349390
|
A | T | 1 | a0001c0005t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.208-1509T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349390 | ||||||
| chr12:121349537
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.208-1656C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349537 | ||||||
| chr12:121349576
|
A | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02258.hp1 HG02818.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-1695T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349576 | ||||||
| chr12:121349717
|
T | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0002t0001g0144 | 3 | HG03209.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208-1836A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349717 | ||||||
| chr12:121349720
|
A | AT | 151 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(148): Show | 169 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.208-1840dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349720 | ||||||
| chr12:121349720
|
A | ATT | 18 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(15): Show | 18 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.208-1841_208-1840d others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349720 | ||||||
| chr12:121349768
|
T | A | 6 | a0001c0002t0001g0094a0001c0002t0001g0096a0001c0002t0001g0097others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-1887A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349768 | ||||||
| chr12:121349829
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG02109.hp2 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.208-1948G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349829 | ||||||
| chr12:121349851
|
C | A | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-1970G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349851 | ||||||
| chr12:121349852
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.208-1971C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349852 | ||||||
| chr12:121349993
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0002t0001g0144 | 3 | HG03209.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208-2112C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121349993 | ||||||
| chr12:121350003
|
G | A | 2 | a0001c0001t0001g0229a0002c0007t0001g0228 | 2 | HG00741.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.208-2122C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350003 | ||||||
| chr12:121350005
|
C | A | 10 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(7): Show | 10 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-2124G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350005 | ||||||
| chr12:121350299
|
A | G | 144 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(141): Show | 159 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.207+1835T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350299 | ||||||
| chr12:121350310
|
G | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 190 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.207+1824C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350310 | ||||||
| chr12:121350383
|
T | G | 1 | a0001c0008t0002g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.207+1751A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350383 | ||||||
| chr12:121350419
|
T | C | 117 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(114): Show | 131 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.207+1715A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350419 | ||||||
| chr12:121350488
|
C | T | 116 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(113): Show | 130 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.207+1646G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350488 | ||||||
| chr12:121350530
|
A | C | 104 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(101): Show | 118 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.207+1604T>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350530 | ||||||
| chr12:121350537
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.207+1597G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350537 | ||||||
| chr12:121350551
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.207+1583C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350551 | ||||||
| chr12:121350663
|
G | A | 117 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(114): Show | 131 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.207+1471C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350663 | ||||||
| chr12:121350680
|
C | CA | 110 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(107): Show | 123 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.207+1453dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350680 | ||||||
| chr12:121350680
|
C | CAA | 10 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG01975.hp1 HG02258.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+1452_207+1453d others(4): Show |
ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350680 | ||||||
| chr12:121350810
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.207+1324T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350810 | ||||||
| chr12:121351142
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.207+992C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121351142 | ||||||
| chr12:121351463
|
C | CT | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(4): Show | 9 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+670dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121351463 | ||||||
| chr12:121351609
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.207+525G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121351609 | ||||||
| chr12:121351757
|
C | A | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(96): Show | 113 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.207+377G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121351757 | ||||||
| chr12:121352084
|
T | A | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(96): Show | 113 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.207+50A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121352084 | ||||||
| chr12:121352124
|
C | A | 88 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0016others(85): Show | 100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.207+10G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121352124 |