Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MASVH others(750): Show |
chr12 | 121303245 | 121357411 |
| a0002 | 0/0 | 755 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | MASVH others(750): Show |
chr12 | 121303245 | 121357411 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2265 | 258 | 76 | 53 | 96 | 6 | 25 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | ATGGC others(2260): Show |
chr12 | 121303245 | 121357411 | ||
| a0001c0002 | 0/0 | 2265 | 10 | 8 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | ATGGC others(2260): Show |
chr12 | 121303245 | 121357411 | ||
| a0001c0003 | 0/0 | 2265 | 3 | 0 | 0 | 0 | 0 | 3 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | ATGGC others(2260): Show |
chr12 | 121303245 | 121357411 | ||
| a0001c0004 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | ATGGC others(2260): Show |
chr12 | 121303245 | 121357411 | ||
| a0001c0005 | 0/0 | 2265 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | ATGGC others(2260): Show |
chr12 | 121303245 | 121357411 | ||
| a0001c0006 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | ATGGC others(2260): Show |
chr12 | 121303245 | 121357411 | ||
| a0001c0008 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | ATGGC others(2260): Show |
chr12 | 121303245 | 121357411 | ||
| a0002c0007 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | ATGGC others(2260): Show |
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 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0001c0001t0002 | 0/0 | 2574 | 4 | 3 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0001c0001t0003 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0001c0002t0001 | 0/0 | 2574 | 10 | 8 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0001c0003t0001 | 0/0 | 2574 | 3 | 0 | 0 | 0 | 0 | 3 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0001c0004t0001 | 0/0 | 2574 | 2 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0001c0005t0001 | 0/0 | 2574 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0001c0006t0001 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0001c0008t0002 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
chr12 | 121303245 | 121357411 |
| a0002c0007t0001 | 0/0 | 2574 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | GGTAG others(2569): Show |
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 | 0 | 0 | 3 | 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 | 3 | 0 | 0 | 3 | 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 | 2 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 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 | 2 | 0 | 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 | 2 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0001c0001t0001g0027 | 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 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0053 | 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 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0058 | 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 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0085 | 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 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0099 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0132 | 0/1 | 1 | 0 | 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 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0013 | 0/0 | 2 | 2 | 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 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0001c0008t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| a0002c0007t0001g0225 | 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 | g0024 | EUR | GBR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG00741 | hp2 | a0002 | c0007 | t0001 | g0225 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0160 | 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 | g0131 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0146 | 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 | g0041 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0113 | 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 | g0115 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0040 | 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 | g0179 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0091 | 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 | g0191 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0119 | 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 | g0165 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02083 | hp1 | a0001 | c0005 | t0001 | g0055 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02155 | hp1 | a0001 | c0005 | t0001 | g0032 | EAS | CDX | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0223 | 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 | g0025 | EAS | KHV | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0100 | 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 | g0080 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0093 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0015 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0096 | 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 | g0221 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0195 | 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 | g0079 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0059 | 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 | g0013 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | 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 | g0236 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0029 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0218 | 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 | g0227 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0118 | 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 | g0130 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0057 | 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 | g0085 | 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 | g0102 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | 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 | g0011 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0083 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0015 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0037 | 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 | g0197 | AFR | YRI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | 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 | g0112 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0182 | 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 | g0186 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | 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 | g0174 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | 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 | g0105 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | 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 | g0046 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | 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 | g0200 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | 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 | g0110 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0109 | 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 | g0193 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0039 | 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 | g0224 | 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 | g0017 | AFR | ASW | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0074 | 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 | g0084 | AFR | ACB | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | MSL | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG06807 | hp1 | a0001 | c0008 | t0002 | g0232 | AFR | USA | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0097 | AFR | USA | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0231 | 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 | g0077 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0132 | REF | REF | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0065 | REF | REF | ANAPC5_chr12_121303245_121357411 | ANAPC5 | chr12 | 121303245 | 121357411 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121318281 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121308534 | 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 | a0001c0002 a0001c0004 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121308396 | 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 | a0001c0001t0002 a0001c0008t0002 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121308739 | G | A | 1 | a0001c0001t0001g0161 | 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 | 22 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0040 others(19): Show |
24 | HG00438.hp1 HG00558.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.2057-456dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 16/16 | chr12 | 121309146 | |||||||
| chr12:121309146 | CA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0115 | 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 | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
180 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(177): 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 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | 6 | a0001c0002t0001g0013 a0001c0002t0001g0059 a0001c0002t0001g0060 others(3): 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0082 others(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 | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
100 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(97): 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 | 13 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0016 others(10): 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 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0191 others(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 | a0001c0003t0001g0015 a0001c0003t0001g0083 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0144 |
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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): 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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): 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 | |||||||
| chr12:121311758 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
122 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(119): 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
127 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.1894-2844dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121312706 | |||||||
| chr12:121312706 | C | CAA | 33 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
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 | a0001c0001t0001g0075 | 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 | 5 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0071 others(2): 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0066 |
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 | 37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(34): 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 |
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 | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): 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 | a0001c0001t0001g0157 | 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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
122 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(119): 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 | a0001c0001t0001g0081 | 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 | a0001c0003t0001g0015 a0001c0003t0001g0083 |
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 | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
123 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(120): 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 | a0001c0001t0001g0187 a0001c0001t0001g0208 a0001c0001t0001g0220 |
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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0081 | 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 | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): 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 | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0062 others(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 | 19 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0048 others(16): Show |
21 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1893+1544delT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316732 | |||||||
| chr12:121316732 | CAA | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): 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 | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
274 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.1893+1363G>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121316914 | |||||||
| chr12:121317253 | CT | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0079 others(12): Show |
16 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1893+1023delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317253 | |||||||
| chr12:121317323 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 |
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 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
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 | a0001c0001t0002g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1893+863G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 15/16 | chr12 | 121317414 | |||||||
| chr12:121317549 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
122 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(119): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
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 | a0001c0001t0001g0138 a0001c0008t0002g0232 |
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 | 44 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(41): 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 | a0001c0001t0001g0221 | 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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
122 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(119): Show |
intron_variant | MODIFIER | c.1638-231C>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121318839 | |||||||
| chr12:121318881 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0104 a0001c0001t0001g0195 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0133 others(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 | 26 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0085 others(23): Show |
28 | HG01069.hp1 HG01099.hp2 HG01109.hp2 others(25): 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0026 others(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 | 34 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(31): 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0216 |
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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
115 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(112): Show |
intron_variant | MODIFIER | c.1637+459delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 13/16 | chr12 | 121319237 | |||||||
| chr12:121319297 | A | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0196 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0196 |
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 | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
123 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(120): Show |
intron_variant | MODIFIER | c.1516-39C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 12/16 | chr12 | 121319857 | |||||||
| chr12:121319954 | T | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
122 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(119): 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 | a0001c0001t0001g0110 a0001c0001t0001g0127 |
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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
121 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(118): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0002g0233 a0001c0001t0002g0236 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 |
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 | 10 | a0001c0002t0001g0013 a0001c0002t0001g0059 a0001c0002t0001g0060 others(7): 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 | a0001c0001t0002g0233 a0001c0001t0002g0236 |
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 | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(38): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | 54 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(51): Show |
63 | HG00558.hp1 HG01099.hp2 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.1441-885dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121321343 | |||||||
| chr12:121321343 | C | CTT | 8 | a0001c0001t0001g0071 a0001c0001t0001g0106 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0017 | 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 | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0082 | 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 | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(38): 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 | 11 | a0001c0002t0001g0013 a0001c0002t0001g0059 a0001c0002t0001g0060 others(8): 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 | a0001c0001t0001g0146 | 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 | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): 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 | a0001c0001t0001g0219 | 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 | 19 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0129 others(16): Show |
20 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.1441-1707dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121322165 | |||||||
| chr12:121322379 | C | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0169 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0222 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): 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 | 42 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(39): 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 | 26 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(23): 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 | 2 | a0001c0001t0001g0014 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0115 | 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 | a0001c0003t0001g0083 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0144 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0008t0002g0232 |
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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0115 | 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 | a0001c0003t0001g0015 a0001c0003t0001g0083 |
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 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
226 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(223): 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 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0176 a0001c0001t0001g0206 |
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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
118 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(115): Show |
intron_variant | MODIFIER | c.1440+1589dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 11/16 | chr12 | 121325506 | |||||||
| chr12:121325511 | A | AT | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(123): 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 | a0001c0001t0001g0198 | 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 | 42 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(39): 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 | a0001c0001t0001g0038 a0001c0001t0001g0114 a0001c0001t0001g0128 others(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 | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
226 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(223): 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 | a0001c0001t0001g0116 | 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 | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): 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 | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
227 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(224): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0106 | 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 | 11 | a0001c0002t0001g0013 a0001c0002t0001g0059 a0001c0002t0001g0060 others(8): 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 | 10 | a0001c0002t0001g0013 a0001c0002t0001g0059 a0001c0002t0001g0060 others(7): 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0162 | 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 | 23 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(20): 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(202): Show |
237 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(234): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(123): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0116 | 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 | 9 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0131 others(6): Show |
9 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(6): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0031 | 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 | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
173 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.951-1090A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332518 | |||||||
| chr12:121332577 | G | GT | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
220 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.951-1150dupA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121332577 | |||||||
| chr12:121332621 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(52): Show |
63 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(60): 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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0081 | 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 | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0081 | 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 | 29 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(26): 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0200 | 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 | 20 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(17): 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 | a0001c0008t0002g0232 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0002t0001g0092 others(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 | a0001c0001t0001g0163 | 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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.950+806G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121334727 | |||||||
| chr12:121334986 | TC | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(32): 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 | a0001c0001t0001g0081 | 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 | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.950+455A>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121335078 | |||||||
| chr12:121335166 | A | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.950+367T>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 7/16 | chr12 | 121335166 | |||||||
| chr12:121335227 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0098 |
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 | a0001c0002t0001g0096 | 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 | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(127): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0201 | 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 | 12 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0081 others(9): Show |
13 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(10): 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 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
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 | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(183): Show |
217 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(214): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0002g0234 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0049 others(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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): 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 | a0001c0006t0001g0029 | 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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0205 | 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 | 26 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(23): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): 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 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0105 |
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 | a0001c0001t0001g0073 | 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 | 43 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(40): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | 4 | a0001c0002t0001g0013 a0001c0002t0001g0059 a0001c0002t0001g0060 others(1): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0003t0001g0015 others(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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.658-1120A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121338512 | |||||||
| chr12:121338654 | T | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0207 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0070 others(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 | 16 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0129 others(13): Show |
17 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.658-1663delA | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339054 | |||||||
| chr12:121339055 | T | C | 1 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0002t0001g0092 others(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 | a0001c0001t0001g0038 | 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 | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(38): 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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.658-2168A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339560 | |||||||
| chr12:121339619 | T | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.658-2227A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339619 | |||||||
| chr12:121339657 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.658-2265G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339657 | |||||||
| chr12:121339749 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(185): Show |
219 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(216): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0077 | 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 | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(63): 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 | 9 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0067 others(6): Show |
9 | HG01099.hp2 HG01243.hp1 HG01358.hp2 others(6): 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 | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(35): 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0205 | 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 | a0001c0003t0001g0015 a0001c0003t0001g0083 |
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 | a0001c0001t0001g0078 | 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 | 27 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(24): 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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.657+2057C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121339946 | |||||||
| chr12:121340041 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0067 others(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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.657+1760C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340243 | |||||||
| chr12:121340316 | C | CA | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(41): 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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0039 | 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 | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): 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 | a0001c0001t0001g0153 | 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 | a0001c0003t0001g0083 | 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 | a0001c0001t0001g0082 | 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 | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(123): 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 | 10 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(7): Show |
11 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.657+1006A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121340997 | |||||||
| chr12:121341102 | T | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
235 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(232): Show |
intron_variant | MODIFIER | c.657+901A>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 5/16 | chr12 | 121341102 | |||||||
| chr12:121341198 | G | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(24): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | 4 | a0001c0002t0001g0013 a0001c0002t0001g0059 a0001c0002t0001g0060 others(1): 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | 17 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0081 others(14): Show |
18 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(15): 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0003t0001g0015 a0001c0003t0001g0083 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
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 | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.591-721A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 4/16 | chr12 | 121342790 | |||||||
| chr12:121342808 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0131 others(8): Show |
12 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(9): 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 |
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 | a0001c0001t0001g0091 a0001c0003t0001g0015 a0001c0003t0001g0083 |
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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0037 a0001c0002t0001g0092 a0001c0002t0001g0094 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0002g0233 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0125 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0082 | 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 | 9 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(6): 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0002t0001g0142 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0002t0001g0142 |
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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0027 | 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 | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0216 a0001c0001t0001g0217 |
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 | 9 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(6): 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 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
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 | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): 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 | a0001c0001t0001g0162 | 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 | a0001c0002t0001g0092 a0001c0002t0001g0094 a0001c0002t0001g0095 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0160 a0001c0001t0001g0161 |
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 | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
158 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(155): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0081 | 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 | a0001c0003t0001g0083 | 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 | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): 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 | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): 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 | 179 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
200 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(197): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0159 |
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 | a0001c0005t0001g0032 | 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0139 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0002t0001g0142 |
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 | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): 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 | 17 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(14): Show |
17 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(14): 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 | a0001c0002t0001g0092 a0001c0002t0001g0094 a0001c0002t0001g0095 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0002t0001g0142 |
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 | a0001c0001t0001g0226 a0002c0007t0001g0225 |
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 | 9 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-2124G>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350005 | |||||||
| chr12:121350299 | A | G | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
158 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.207+1835T>C | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350299 | |||||||
| chr12:121350310 | G | A | 170 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
189 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(186): 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 | a0001c0008t0002g0232 | 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 | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
130 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.207+1715A>G | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350419 | |||||||
| chr12:121350488 | C | T | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
129 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.207+1646G>A | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350488 | |||||||
| chr12:121350530 | A | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
130 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.207+1471C>T | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350663 | |||||||
| chr12:121350680 | C | CA | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
122 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.207+1453dupT | ANAPC5 | ENSG00000089053.13 | transcript | ENST00000261819.8 | protein_coding | 1/16 | chr12 | 121350680 | |||||||
| chr12:121350680 | C | CAA | 10 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0026 | 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 | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): 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 | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): 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 | 87 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): 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 |