Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55832 |
| ensemblid | ENSG00000111530.13 |
| hgncid | 30688 |
| symbol | CAND1 |
| name | cullin associated and neddylation dissociated 1 |
| refseq_nuc | NM_018448.5 |
| refseq_prot | NP_060918.2 |
| ensembl_nuc | ENST00000545606.6 |
| ensembl_prot | ENSP00000442318.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 67269358 |
| end | 67319953 |
| strand | + |
| ver | v1.2 |
| region | chr12:67269358-67319953 |
| region5000 | chr12:67264358-67324953 |
| regionname0 | CAND1_chr12_67269358_67319953 |
| regionname5000 | CAND1_chr12_67264358_67324953 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1230 | 325 | 82 | 49 | 142 | 12 | 38 | 112 | CAND1_chr12_67264358_67324953 | CAND1 | MASAS others(1225): Show |
chr12 | 67264358 | 67324953 |
| a0002 | 0/0 | 1230 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | MASAS others(1225): Show |
chr12 | 67264358 | 67324953 |
| a0003 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | MASAS others(1225): Show |
chr12 | 67264358 | 67324953 |
| a0004 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | MASAS others(1225): Show |
chr12 | 67264358 | 67324953 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3690 | 201 | 59 | 25 | 87 | 3 | 25 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0002 | 0/0 | 3690 | 103 | 11 | 22 | 52 | 6 | 12 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0003 | 0/0 | 3690 | 7 | 1 | 2 | 0 | 3 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0004 | 0/0 | 3690 | 6 | 6 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0005 | 0/0 | 3690 | 3 | 3 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0007 | 0/0 | 3690 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0009 | 0/0 | 3690 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0011 | 0/0 | 3690 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0012 | 0/0 | 3690 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0001c0013 | 0/0 | 3690 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0002c0008 | 0/0 | 3690 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0003c0006 | 0/0 | 3690 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 | ||
| a0004c0010 | 0/0 | 3690 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | ATGGC others(3685): Show |
chr12 | 67264358 | 67324953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 11174 | 35 | 0 | 2 | 26 | 1 | 6 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0003 | 1/0 | 11176 | 36 | 4 | 9 | 13 | 1 | 8 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0004 | 0/0 | 11176 | 14 | 0 | 4 | 8 | 0 | 2 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0005 | 0/0 | 11173 | 13 | 0 | 1 | 9 | 0 | 3 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0006 | 0/0 | 11173 | 10 | 0 | 0 | 10 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0007 | 0/0 | 11173 | 9 | 6 | 3 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0008 | 0/0 | 11177 | 9 | 0 | 0 | 9 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0011 | 0/0 | 11173 | 6 | 6 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0012 | 0/0 | 11173 | 6 | 6 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0013 | 0/0 | 11176 | 5 | 5 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0015 | 0/0 | 11177 | 4 | 2 | 0 | 2 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0017 | 0/0 | 11173 | 3 | 3 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0018 | 0/0 | 11172 | 3 | 3 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11167): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0019 | 0/0 | 11175 | 3 | 0 | 1 | 1 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0020 | 0/0 | 11177 | 3 | 3 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0021 | 0/0 | 11175 | 3 | 3 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0022 | 0/0 | 11174 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0023 | 0/0 | 11174 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0024 | 0/0 | 11176 | 2 | 0 | 0 | 2 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0025 | 0/0 | 11177 | 2 | 0 | 0 | 1 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0026 | 0/0 | 11177 | 2 | 0 | 0 | 0 | 0 | 2 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0027 | 0/0 | 11175 | 2 | 0 | 1 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0028 | 0/0 | 11173 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0030 | 0/1 | 11182 | 1 | 0 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11177): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0031 | 0/0 | 11175 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0032 | 0/0 | 11176 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0033 | 0/0 | 11172 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11167): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0034 | 0/0 | 11173 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0035 | 0/0 | 11173 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0036 | 0/0 | 11174 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0037 | 0/0 | 11174 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0038 | 0/0 | 11183 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11178): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0039 | 0/0 | 11173 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0040 | 0/0 | 11173 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0041 | 0/0 | 11176 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0042 | 0/0 | 11176 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0043 | 0/0 | 11176 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0044 | 0/0 | 11177 | 1 | 0 | 0 | 0 | 1 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0045 | 0/0 | 11174 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0046 | 0/0 | 11173 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11168): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0056 | 0/0 | 11175 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0057 | 0/0 | 11175 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0058 | 0/0 | 11176 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0059 | 0/0 | 11174 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0060 | 0/0 | 11174 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0061 | 0/0 | 11174 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0062 | 0/0 | 11206 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11201): Show |
chr12 | 67264358 | 67324953 |
| a0001c0001t0065 | 0/0 | 11176 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0001 | 0/0 | 11176 | 83 | 10 | 18 | 39 | 6 | 10 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0009 | 0/0 | 11177 | 9 | 1 | 0 | 8 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0016 | 0/0 | 11177 | 3 | 0 | 3 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0048 | 0/0 | 11177 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0049 | 0/0 | 11177 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0050 | 0/0 | 11143 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11138): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0051 | 0/0 | 11175 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0052 | 0/0 | 11176 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0053 | 0/0 | 11176 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0054 | 0/0 | 11176 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0002t0055 | 0/0 | 11176 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0003t0010 | 0/0 | 11175 | 6 | 0 | 2 | 0 | 3 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0003t0063 | 0/0 | 11176 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0004t0014 | 0/0 | 11175 | 5 | 5 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0001c0004t0047 | 0/0 | 11172 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11167): Show |
chr12 | 67264358 | 67324953 |
| a0001c0005t0029 | 0/0 | 11177 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11172): Show |
chr12 | 67264358 | 67324953 |
| a0001c0005t0064 | 0/0 | 11178 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11173): Show |
chr12 | 67264358 | 67324953 |
| a0001c0007t0002 | 0/0 | 11174 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0001c0009t0001 | 0/0 | 11176 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0011t0001 | 0/0 | 11176 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0012t0001 | 0/0 | 11176 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0001c0013t0001 | 0/0 | 11176 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| a0002c0008t0010 | 0/0 | 11175 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11170): Show |
chr12 | 67264358 | 67324953 |
| a0003c0006t0002 | 0/0 | 11174 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11169): Show |
chr12 | 67264358 | 67324953 |
| a0004c0010t0001 | 0/0 | 11176 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | CTTTT others(11171): Show |
chr12 | 67264358 | 67324953 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 16 | 0 | 1 | 11 | 1 | 3 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0003 | 0/0 | 11 | 0 | 6 | 2 | 0 | 3 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0006g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0007g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0008g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0008g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0011g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0012g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0013g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0015g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0015g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0015g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0017g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0017g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0018g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0018g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0019g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0019g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0020g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0020g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0021g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0021g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0022g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0022g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0023g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0023g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0024g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0024g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0025g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0025g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0026g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0027g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0027g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0028g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0028g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0030g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0031g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0032g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0033g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0034g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0035g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0036g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0037g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0038g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0039g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0040g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0041g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0042g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0043g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0044g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0045g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0046g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0056g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0057g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0058g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0059g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0060g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0061g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0062g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0001t0065g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0001 | 0/0 | 22 | 1 | 5 | 13 | 2 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0009g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0009g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0009g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0009g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0016g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0016g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0016g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0048g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0049g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0050g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0051g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0052g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0053g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0054g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0002t0055g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0003t0010g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0003t0010g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0003t0010g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0003t0010g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0003t0010g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0003t0063g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0004t0014g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0004t0014g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0004t0014g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0004t0014g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0004t0047g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0005t0029g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0005t0029g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0005t0064g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0007t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0009t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0011t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0001c0013t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0002c0008t0010g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0003c0006t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| a0004c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0123 | EUR | GBR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00099 | hp2 | a0001 | c0003 | t0010 | g0085 | EUR | GBR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0030 | EUR | GBR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00140 | hp2 | a0001 | c0001 | t0044 | g0176 | EUR | GBR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00597 | hp2 | a0001 | c0001 | t0008 | g0166 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00609 | hp2 | a0001 | c0002 | t0009 | g0001 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00639 | hp2 | a0001 | c0003 | t0010 | g0084 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | CHS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00733 | hp1 | a0001 | c0001 | t0041 | g0035 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01069 | hp1 | a0001 | c0001 | t0060 | g0048 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0093 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01109 | hp1 | a0001 | c0001 | t0045 | g0067 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01168 | hp2 | a0001 | c0001 | t0019 | g0160 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01255 | hp2 | a0001 | c0002 | t0016 | g0107 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0096 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01261 | hp2 | a0001 | c0003 | t0010 | g0086 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01346 | hp1 | a0001 | c0002 | t0054 | g0102 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01361 | hp1 | a0001 | c0001 | t0038 | g0005 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01361 | hp2 | a0001 | c0002 | t0016 | g0135 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01496 | hp2 | a0002 | c0008 | t0010 | g0082 | AMR | CLM | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0130 | EUR | IBS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01516 | hp2 | a0001 | c0003 | t0010 | g0020 | EUR | IBS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01517 | hp1 | a0001 | c0003 | t0010 | g0020 | EUR | IBS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0142 | EUR | IBS | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01884 | hp1 | a0001 | c0005 | t0029 | g0080 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01891 | hp1 | a0001 | c0001 | t0018 | g0023 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01928 | hp2 | a0001 | c0002 | t0016 | g0010 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01975 | hp2 | a0001 | c0001 | t0027 | g0011 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0092 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02040 | hp2 | a0001 | c0002 | t0053 | g0143 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02055 | hp1 | a0001 | c0001 | t0035 | g0047 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02071 | hp2 | a0001 | c0002 | t0049 | g0001 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02129 | hp2 | a0001 | c0001 | t0019 | g0159 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02132 | hp2 | a0001 | c0001 | t0061 | g0041 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02145 | hp1 | a0001 | c0001 | t0036 | g0005 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02145 | hp2 | a0001 | c0001 | t0033 | g0070 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0052 | EAS | CDX | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | CDX | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02257 | hp1 | a0001 | c0004 | t0014 | g0075 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02258 | hp2 | a0001 | c0001 | t0032 | g0043 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02280 | hp1 | a0001 | c0001 | t0034 | g0042 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02280 | hp2 | a0001 | c0004 | t0014 | g0074 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02451 | hp1 | a0001 | c0001 | t0022 | g0194 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02523 | hp1 | a0001 | c0002 | t0055 | g0139 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | KHV | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02572 | hp2 | a0001 | c0004 | t0047 | g0076 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02615 | hp1 | a0001 | c0003 | t0063 | g0083 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0068 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02622 | hp2 | a0001 | c0001 | t0023 | g0097 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02630 | hp1 | a0001 | c0001 | t0022 | g0195 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02630 | hp2 | a0001 | c0001 | t0028 | g0066 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0069 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02647 | hp2 | a0001 | c0001 | t0013 | g0078 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02717 | hp1 | a0001 | c0001 | t0065 | g0022 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02735 | hp1 | a0001 | c0002 | t0050 | g0128 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02735 | hp2 | a0001 | c0001 | t0019 | g0003 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02738 | hp1 | a0001 | c0001 | t0026 | g0006 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02809 | hp1 | a0001 | c0001 | t0031 | g0073 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0071 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02895 | hp1 | a0001 | c0011 | t0001 | g0099 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0045 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02922 | hp1 | a0001 | c0005 | t0064 | g0079 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02922 | hp2 | a0001 | c0001 | t0013 | g0072 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02965 | hp2 | a0001 | c0001 | t0018 | g0023 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02976 | hp1 | a0001 | c0001 | t0037 | g0063 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02976 | hp2 | a0001 | c0013 | t0001 | g0001 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0183 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0090 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03041 | hp2 | a0001 | c0001 | t0039 | g0005 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03130 | hp2 | a0001 | c0001 | t0020 | g0022 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03139 | hp2 | a0001 | c0001 | t0021 | g0021 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03209 | hp1 | a0001 | c0001 | t0040 | g0005 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03209 | hp2 | a0001 | c0004 | t0014 | g0019 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0044 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03239 | hp1 | a0001 | c0003 | t0010 | g0087 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03453 | hp2 | a0001 | c0001 | t0021 | g0021 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0046 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0060 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | ESN | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03540 | hp1 | a0001 | c0001 | t0023 | g0091 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | GWD | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03579 | hp2 | a0001 | c0001 | t0021 | g0089 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03654 | hp1 | a0001 | c0001 | t0027 | g0175 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03654 | hp2 | a0001 | c0002 | t0052 | g0001 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | STU | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0141 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0050 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0126 | SAS | BEB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | BEB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03942 | hp1 | a0001 | c0001 | t0025 | g0152 | SAS | BEB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03942 | hp2 | a0001 | c0001 | t0026 | g0006 | SAS | BEB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG04115 | hp1 | a0001 | c0001 | t0059 | g0004 | SAS | STU | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0173 | SAS | STU | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | BEB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | STU | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | STU | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | STU | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18522 | hp1 | a0001 | c0001 | t0028 | g0065 | AFR | YRI | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | YRI | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | YRI | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18906 | hp2 | a0001 | c0001 | t0020 | g0037 | AFR | YRI | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18939 | hp2 | a0001 | c0009 | t0001 | g0136 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18940 | hp1 | a0003 | c0006 | t0002 | g0180 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18941 | hp2 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18944 | hp1 | a0001 | c0007 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18947 | hp2 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18949 | hp1 | a0001 | c0002 | t0009 | g0118 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18949 | hp2 | a0001 | c0001 | t0015 | g0197 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18953 | hp1 | a0001 | c0002 | t0009 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18953 | hp2 | a0001 | c0001 | t0008 | g0193 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18963 | hp1 | a0001 | c0001 | t0042 | g0003 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18969 | hp1 | a0001 | c0001 | t0043 | g0034 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18972 | hp1 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18982 | hp2 | a0001 | c0002 | t0009 | g0114 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18983 | hp2 | a0001 | c0001 | t0015 | g0016 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18990 | hp1 | a0004 | c0010 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18991 | hp1 | a0001 | c0002 | t0009 | g0132 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18994 | hp1 | a0001 | c0001 | t0024 | g0156 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19000 | hp1 | a0001 | c0002 | t0048 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19000 | hp2 | a0001 | c0001 | t0025 | g0163 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19003 | hp1 | a0001 | c0002 | t0009 | g0115 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19006 | hp2 | a0001 | c0001 | t0057 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19010 | hp1 | a0001 | c0002 | t0009 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19011 | hp1 | a0001 | c0012 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19012 | hp1 | a0001 | c0001 | t0058 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19012 | hp2 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19030 | hp1 | a0001 | c0001 | t0015 | g0036 | AFR | LWK | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19030 | hp2 | a0001 | c0001 | t0018 | g0098 | AFR | LWK | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19043 | hp1 | a0001 | c0001 | t0046 | g0039 | AFR | LWK | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19043 | hp2 | a0001 | c0005 | t0029 | g0081 | AFR | LWK | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19060 | hp1 | a0001 | c0001 | t0056 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19063 | hp2 | a0001 | c0001 | t0024 | g0167 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19087 | hp2 | a0001 | c0002 | t0009 | g0001 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19091 | hp1 | a0001 | c0002 | t0051 | g0112 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | YRI | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0061 | AFR | YRI | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | TSI | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0131 | SAS | GIH | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02109 | hp2 | a0001 | c0004 | t0014 | g0019 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0018 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0036 | AFR | ACB | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG03471 | hp2 | a0001 | c0001 | t0062 | g0145 | AFR | MSL | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG06807 | hp1 | a0001 | c0004 | t0014 | g0077 | AFR | USA | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| HG06807 | hp2 | a0001 | c0001 | t0020 | g0088 | AFR | USA | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA18955 | hp2 | a0001 | c0001 | t0008 | g0164 | EAS | JPT | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA21309 | hp1 | a0001 | c0002 | t0009 | g0109 | AFR | LWK | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | LWK | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0030 | g0154 | REF | REF | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0151 | REF | REF | CAND1_chr12_67264358_67324953 | CAND1 | chr12 | 67264358 | 67324953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:67292627 | G | A | 1 | a0003 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.218G>A | p.Gly73Asp | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/15 | 578/11176 | 218/3693 | 73/1230 | chr12 | 67292627 | |||
| chr12:67292629 | C | A | 1 | a0003 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.220C>A | p.Pro74Thr | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/15 | 580/11176 | 220/3693 | 74/1230 | chr12 | 67292629 | |||
| chr12:67292632 | T | A | 1 | a0003 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.223T>A | p.Leu75Ile | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/15 | 583/11176 | 223/3693 | 75/1230 | chr12 | 67292632 | |||
| chr12:67292639 | G | T | 1 | a0003 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.230G>T | p.Ser77Ile | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/15 | 590/11176 | 230/3693 | 77/1230 | chr12 | 67292639 | |||
| chr12:67292640 | T | G | 1 | a0003 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.231T>G | p.Ser77Arg | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/15 | 591/11176 | 231/3693 | 77/1230 | chr12 | 67292640 | |||
| chr12:67292641 | A | T | 1 | a0003 | 1 | NA18940.hp1 | stop_gained | HIGH | c.232A>T | p.Lys78* | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/15 | 592/11176 | 232/3693 | 78/1230 | chr12 | 67292641 | |||
| chr12:67292642 | A | T | 1 | a0003 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.233A>T | p.Lys78Ile | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/15 | 593/11176 | 233/3693 | 78/1230 | chr12 | 67292642 | |||
| chr12:67305239 | T | C | 1 | a0002 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1571T>C | p.Val524Ala | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/15 | 1931/11176 | 1571/3693 | 524/1230 | chr12 | 67305239 | |||
| chr12:67306076 | T | C | 1 | a0004 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.2408T>C | p.Val803Ala | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/15 | 2768/11176 | 2408/3693 | 803/1230 | chr12 | 67306076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:67299007 | T | C | 1 | a0001c0007 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.912T>C | p.Tyr304Tyr | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/15 | 1272/11176 | 912/3693 | 304/1230 | chr12 | 67299007 | |||
| chr12:67302510 | C | T | 1 | a0001c0013 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1188C>T | p.His396His | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/15 | 1548/11176 | 1188/3693 | 396/1230 | chr12 | 67302510 | |||
| chr12:67305177 | A | C | 1 | a0001c0005 | 3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.1509A>C | p.Val503Val | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/15 | 1869/11176 | 1509/3693 | 503/1230 | chr12 | 67305177 | |||
| chr12:67305600 | G | A | 1 | a0001c0009 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.1932G>A | p.Leu644Leu | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/15 | 2292/11176 | 1932/3693 | 644/1230 | chr12 | 67305600 | |||
| chr12:67305687 | C | T | 1 | a0001c0012 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.2019C>T | p.Ala673Ala | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/15 | 2379/11176 | 2019/3693 | 673/1230 | chr12 | 67305687 | |||
| chr12:67305756 | G | A | 2 | a0001c0003 a0002c0008 |
8 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(5): Show |
synonymous_variant | LOW | c.2088G>A | p.Glu696Glu | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/15 | 2448/11176 | 2088/3693 | 696/1230 | chr12 | 67305756 | |||
| chr12:67306344 | G | A | 1 | a0001c0004 | 6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
synonymous_variant | LOW | c.2676G>A | p.Leu892Leu | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/15 | 3036/11176 | 2676/3693 | 892/1230 | chr12 | 67306344 | |||
| chr12:67309992 | A | G | 1 | a0001c0005 | 3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.3117A>G | p.Ser1039Ser | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 12/15 | 3477/11176 | 3117/3693 | 1039/1230 | chr12 | 67309992 | |||
| chr12:67312686 | G | A | 6 | a0001c0002 a0001c0009 a0001c0011 others(3): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
synonymous_variant | LOW | c.3549G>A | p.Leu1183Leu | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3909/11176 | 3549/3693 | 1183/1230 | chr12 | 67312686 | |||
| chr12:67312764 | G | A | 1 | a0001c0011 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.3627G>A | p.Ala1209Ala | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3987/11176 | 3627/3693 | 1209/1230 | chr12 | 67312764 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:67269428 | C | T | 8 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0065 others(5): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-290C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/15 | chr12 | 67269428 | |||||||
| chr12:67269643 | T | TGGCGGCG others(23): Show |
1 | a0001c0001t0062 | 1 | HG03471.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57_-56insGGCGGCGG others(22): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/15 | 56 | INFO_REALIGN_3_PRIME | chr12 | 67269643 | |||||
| chr12:67313071 | C | T | 5 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0059 others(2): Show |
26 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*241C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 241 | chr12 | 67313071 | ||||||
| chr12:67313337 | CAG | C | 6 | a0001c0001t0002 a0001c0001t0056 a0001c0001t0057 others(3): Show |
40 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*512_*513delAG | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 512 | INFO_REALIGN_3_PRIME | chr12 | 67313337 | |||||
| chr12:67313353 | T | C | 7 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0022 others(4): Show |
17 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*523T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 523 | chr12 | 67313353 | ||||||
| chr12:67313410 | C | A | 1 | a0001c0002t0016 | 3 | HG01255.hp2 HG01361.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*580C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 580 | chr12 | 67313410 | ||||||
| chr12:67313411 | G | A | 1 | a0001c0001t0035 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 581 | chr12 | 67313411 | ||||||
| chr12:67313450 | C | T | 1 | a0001c0001t0065 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 620 | chr12 | 67313450 | ||||||
| chr12:67313484 | T | C | 2 | a0001c0001t0017 a0001c0001t0035 |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*654T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 654 | chr12 | 67313484 | ||||||
| chr12:67313661 | A | G | 16 | a0001c0002t0001 a0001c0002t0009 a0001c0002t0016 others(13): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*831A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 831 | chr12 | 67313661 | ||||||
| chr12:67313664 | A | G | 1 | a0001c0001t0058 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*834A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 834 | chr12 | 67313664 | ||||||
| chr12:67314422 | T | C | 1 | a0001c0002t0016 | 3 | HG01255.hp2 HG01361.hp2 HG01928.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1592T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 1592 | chr12 | 67314422 | ||||||
| chr12:67314641 | G | A | 9 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0018 others(6): Show |
25 | HG01069.hp2 HG01261.hp1 HG01361.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1811G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 1811 | chr12 | 67314641 | ||||||
| chr12:67314763 | C | T | 59 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(56): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1933C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 1933 | chr12 | 67314763 | ||||||
| chr12:67314848 | A | AT | 2 | a0001c0005t0029 a0001c0005t0064 |
3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2019dupT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2020 | INFO_REALIGN_3_PRIME | chr12 | 67314848 | |||||
| chr12:67314889 | A | G | 4 | a0001c0001t0004 a0001c0001t0026 a0001c0001t0027 others(1): Show |
19 | HG00140.hp2 HG00438.hp2 HG01358.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2059A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2059 | chr12 | 67314889 | ||||||
| chr12:67315020 | C | T | 6 | a0001c0001t0002 a0001c0001t0056 a0001c0001t0057 others(3): Show |
40 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2190C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2190 | chr12 | 67315020 | ||||||
| chr12:67315181 | G | A | 1 | a0001c0001t0045 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2351G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2351 | chr12 | 67315181 | ||||||
| chr12:67315255 | C | T | 2 | a0001c0005t0029 a0001c0005t0064 |
3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2425C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2425 | chr12 | 67315255 | ||||||
| chr12:67315408 | G | A | 1 | a0001c0001t0045 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2578G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2578 | chr12 | 67315408 | ||||||
| chr12:67315450 | C | CA | 11 | a0001c0001t0015 a0001c0001t0018 a0001c0001t0026 others(8): Show |
18 | HG00733.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2640dupA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2641 | INFO_REALIGN_3_PRIME | chr12 | 67315450 | |||||
| chr12:67315450 | C | CAA | 16 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(13): Show |
54 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2639_*2640dupAA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2641 | INFO_REALIGN_3_PRIME | chr12 | 67315450 | |||||
| chr12:67315450 | C | CAAA | 7 | a0001c0001t0013 a0001c0001t0023 a0001c0001t0031 others(4): Show |
16 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2638_*2640dupAAA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2641 | INFO_REALIGN_3_PRIME | chr12 | 67315450 | |||||
| chr12:67315460 | A | AG | 2 | a0001c0001t0008 a0001c0001t0043 |
10 | HG00597.hp2 NA18941.hp2 NA18947.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2630_*2631insG | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2631 | chr12 | 67315460 | ||||||
| chr12:67315557 | C | T | 2 | a0001c0001t0032 a0001c0001t0034 |
2 | HG02258.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2727C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2727 | chr12 | 67315557 | ||||||
| chr12:67315610 | C | T | 28 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(25): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2780C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2780 | chr12 | 67315610 | ||||||
| chr12:67315656 | A | G | 1 | a0001c0001t0046 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2826A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2826 | chr12 | 67315656 | ||||||
| chr12:67315679 | ATAAT | A | 28 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(25): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2853_*2856delTTAA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 2853 | INFO_REALIGN_3_PRIME | chr12 | 67315679 | |||||
| chr12:67315856 | T | C | 25 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0062 others(22): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*3026T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3026 | chr12 | 67315856 | ||||||
| chr12:67315861 | A | G | 1 | a0001c0001t0044 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3031A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3031 | chr12 | 67315861 | ||||||
| chr12:67315920 | A | G | 9 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0018 others(6): Show |
25 | HG01069.hp2 HG01261.hp1 HG01361.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3090A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3090 | chr12 | 67315920 | ||||||
| chr12:67315984 | T | C | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3154T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3154 | chr12 | 67315984 | ||||||
| chr12:67315987 | C | T | 2 | a0001c0001t0006 a0001c0001t0061 |
11 | HG00673.hp1 HG02083.hp2 HG02132.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3157C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3157 | chr12 | 67315987 | ||||||
| chr12:67315992 | G | T | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3162G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3162 | chr12 | 67315992 | ||||||
| chr12:67315993 | A | T | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3163A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3163 | chr12 | 67315993 | ||||||
| chr12:67315999 | A | T | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3169A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3169 | chr12 | 67315999 | ||||||
| chr12:67316000 | T | C | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3170T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3170 | chr12 | 67316000 | ||||||
| chr12:67316011 | A | G | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3181A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3181 | chr12 | 67316011 | ||||||
| chr12:67316012 | A | C | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3182 | chr12 | 67316012 | ||||||
| chr12:67316020 | TCTCTGGA others(26): Show |
T | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3191_*3223delCTCT others(29): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3191 | chr12 | 67316020 | ||||||
| chr12:67316068 | A | C | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3238A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3238 | chr12 | 67316068 | ||||||
| chr12:67316070 | C | T | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3240C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3240 | chr12 | 67316070 | ||||||
| chr12:67316072 | T | G | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3242T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3242 | chr12 | 67316072 | ||||||
| chr12:67316079 | A | T | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3249A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3249 | chr12 | 67316079 | ||||||
| chr12:67316086 | T | G | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3256T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3256 | chr12 | 67316086 | ||||||
| chr12:67316088 | T | G | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3258T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3258 | chr12 | 67316088 | ||||||
| chr12:67316091 | G | A | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3261G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3261 | chr12 | 67316091 | ||||||
| chr12:67316094 | T | C | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3264T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3264 | chr12 | 67316094 | ||||||
| chr12:67316102 | T | A | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3272T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3272 | chr12 | 67316102 | ||||||
| chr12:67316105 | T | C | 1 | a0001c0002t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3275T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3275 | chr12 | 67316105 | ||||||
| chr12:67316185 | A | T | 16 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0011 others(13): Show |
53 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3355A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3355 | chr12 | 67316185 | ||||||
| chr12:67316288 | A | G | 5 | a0001c0001t0012 a0001c0001t0036 a0001c0001t0038 others(2): Show |
10 | HG01361.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3458A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3458 | chr12 | 67316288 | ||||||
| chr12:67316321 | G | A | 1 | a0001c0001t0062 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3491G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3491 | chr12 | 67316321 | ||||||
| chr12:67316422 | G | A | 5 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0059 others(2): Show |
26 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3592G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3592 | chr12 | 67316422 | ||||||
| chr12:67316511 | G | A | 2 | a0001c0001t0020 a0001c0001t0065 |
4 | HG02717.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3681G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3681 | chr12 | 67316511 | ||||||
| chr12:67316702 | T | C | 16 | a0001c0002t0001 a0001c0002t0009 a0001c0002t0016 others(13): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3872T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 3872 | chr12 | 67316702 | ||||||
| chr12:67316886 | C | T | 1 | a0001c0001t0040 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4056C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4056 | chr12 | 67316886 | ||||||
| chr12:67316962 | A | AACATAGT others(3): Show |
1 | a0001c0001t0038 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4135_*4144dupATAG others(6): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4145 | INFO_REALIGN_3_PRIME | chr12 | 67316962 | |||||
| chr12:67317127 | A | G | 16 | a0001c0002t0001 a0001c0002t0009 a0001c0002t0016 others(13): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*4297A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4297 | chr12 | 67317127 | ||||||
| chr12:67317260 | C | T | 12 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0018 others(9): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4430C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4430 | chr12 | 67317260 | ||||||
| chr12:67317293 | G | A | 1 | a0001c0001t0024 | 2 | NA18994.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4463G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4463 | chr12 | 67317293 | ||||||
| chr12:67317320 | G | A | 25 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0062 others(22): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4490G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4490 | chr12 | 67317320 | ||||||
| chr12:67317369 | T | A | 7 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0022 others(4): Show |
17 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4539T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4539 | chr12 | 67317369 | ||||||
| chr12:67317422 | C | G | 1 | a0001c0002t0049 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4592C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4592 | chr12 | 67317422 | ||||||
| chr12:67317471 | T | A | 1 | a0001c0001t0065 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4641T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4641 | chr12 | 67317471 | ||||||
| chr12:67317471 | TA | T | 2 | a0001c0001t0017 a0001c0001t0035 |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4643delA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4643 | INFO_REALIGN_3_PRIME | chr12 | 67317471 | |||||
| chr12:67317473 | A | AT | 11 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0020 others(8): Show |
33 | HG00140.hp2 HG00609.hp2 HG01255.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4666dupT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4667 | INFO_REALIGN_3_PRIME | chr12 | 67317473 | |||||
| chr12:67317473 | A | T | 1 | a0001c0001t0065 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4643A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4643 | chr12 | 67317473 | ||||||
| chr12:67317473 | AT | A | 23 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(20): Show |
72 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4666delT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4666 | INFO_REALIGN_3_PRIME | chr12 | 67317473 | |||||
| chr12:67317541 | G | C | 1 | a0001c0001t0031 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4711G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4711 | chr12 | 67317541 | ||||||
| chr12:67317614 | C | G | 6 | a0001c0001t0021 a0001c0003t0010 a0001c0003t0063 others(3): Show |
14 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4784C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4784 | chr12 | 67317614 | ||||||
| chr12:67317806 | C | T | 1 | a0001c0002t0055 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4976C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4976 | chr12 | 67317806 | ||||||
| chr12:67317814 | A | T | 2 | a0001c0004t0014 a0001c0004t0047 |
6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4984A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 4984 | chr12 | 67317814 | ||||||
| chr12:67317860 | C | T | 12 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0018 others(9): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5030C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5030 | chr12 | 67317860 | ||||||
| chr12:67317885 | A | G | 1 | a0001c0001t0042 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5055A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5055 | chr12 | 67317885 | ||||||
| chr12:67317887 | C | G | 1 | a0001c0001t0062 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5057C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5057 | chr12 | 67317887 | ||||||
| chr12:67318101 | C | T | 2 | a0001c0005t0029 a0001c0005t0064 |
3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5271C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5271 | chr12 | 67318101 | ||||||
| chr12:67318149 | T | C | 2 | a0001c0001t0020 a0001c0001t0065 |
4 | HG02717.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5319T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5319 | chr12 | 67318149 | ||||||
| chr12:67318169 | T | C | 25 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0062 others(22): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*5339T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5339 | chr12 | 67318169 | ||||||
| chr12:67318294 | A | G | 8 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0065 others(5): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5464A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5464 | chr12 | 67318294 | ||||||
| chr12:67318306 | G | A | 2 | a0001c0001t0017 a0001c0001t0035 |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5476G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5476 | chr12 | 67318306 | ||||||
| chr12:67318794 | G | A | 1 | a0001c0002t0052 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5964G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 5964 | chr12 | 67318794 | ||||||
| chr12:67318876 | T | C | 2 | a0001c0001t0017 a0001c0001t0035 |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6046T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6046 | chr12 | 67318876 | ||||||
| chr12:67318988 | A | G | 28 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(25): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*6158A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6158 | chr12 | 67318988 | ||||||
| chr12:67319198 | A | G | 6 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0065 others(3): Show |
15 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6368A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6368 | chr12 | 67319198 | ||||||
| chr12:67319245 | C | T | 1 | a0001c0002t0054 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6415C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6415 | chr12 | 67319245 | ||||||
| chr12:67319269 | C | T | 28 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(25): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*6439C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6439 | chr12 | 67319269 | ||||||
| chr12:67319342 | T | G | 1 | a0001c0002t0053 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6512T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6512 | chr12 | 67319342 | ||||||
| chr12:67319501 | G | A | 12 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0018 others(9): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6671G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6671 | chr12 | 67319501 | ||||||
| chr12:67319542 | A | G | 8 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0065 others(5): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*6712A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6712 | chr12 | 67319542 | ||||||
| chr12:67319700 | G | A | 1 | a0001c0001t0021 | 3 | HG03139.hp2 HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6870G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6870 | chr12 | 67319700 | ||||||
| chr12:67319716 | T | A | 1 | a0001c0001t0022 | 2 | HG02451.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6886T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 6886 | chr12 | 67319716 | ||||||
| chr12:67319849 | G | T | 1 | a0001c0001t0039 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7019G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 7019 | chr12 | 67319849 | ||||||
| chr12:67319907 | C | T | 1 | a0001c0001t0042 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7077C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 15/15 | 7077 | chr12 | 67319907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:67269931 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.68+146C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67269931 | |||||||
| chr12:67269967 | A | AACCCCCT others(24): Show |
4 | a0001c0001t0003g0016 a0001c0001t0003g0196 a0001c0001t0015g0016 others(1): Show |
5 | NA18949.hp2 NA18957.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+207_68+208insGT others(29): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67269967 | ||||||
| chr12:67270059 | C | T | 2 | a0001c0001t0022g0194 a0001c0001t0022g0195 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.68+274C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270059 | |||||||
| chr12:67270149 | G | A | 1 | a0001c0001t0020g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68+364G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270149 | |||||||
| chr12:67270198 | T | G | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.68+413T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270198 | |||||||
| chr12:67270247 | C | T | 1 | a0001c0001t0008g0193 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.68+462C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270247 | |||||||
| chr12:67270350 | G | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.68+565G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270350 | |||||||
| chr12:67270383 | A | C | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.68+598A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270383 | |||||||
| chr12:67270705 | G | A | 1 | a0001c0001t0005g0038 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.68+920G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270705 | |||||||
| chr12:67270706 | C | T | 1 | a0001c0001t0020g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68+921C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270706 | |||||||
| chr12:67270746 | T | C | 1 | a0001c0001t0004g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68+961T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270746 | |||||||
| chr12:67270769 | TA | T | 29 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0003g0035 others(26): Show |
38 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.68+1001delA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67270769 | ||||||
| chr12:67270769 | TAA | T | 153 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0178 others(150): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.68+1000_68+1001del others(2): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67270769 | ||||||
| chr12:67270769 | TAAA | T | 13 | a0001c0001t0007g0090 a0001c0001t0007g0092 a0001c0001t0007g0093 others(10): Show |
14 | HG01069.hp2 HG01261.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.68+999_68+1001delA others(2): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67270769 | ||||||
| chr12:67270788 | A | G | 1 | a0001c0001t0020g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.68+1003A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270788 | |||||||
| chr12:67270798 | C | T | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.68+1013C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270798 | |||||||
| chr12:67270832 | G | A | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.68+1047G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67270832 | |||||||
| chr12:67271038 | A | G | 10 | a0001c0001t0007g0090 a0001c0001t0007g0092 a0001c0001t0007g0093 others(7): Show |
11 | HG01069.hp2 HG01261.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.68+1253A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271038 | |||||||
| chr12:67271059 | A | G | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.68+1274A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271059 | |||||||
| chr12:67271091 | A | C | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.68+1306A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271091 | |||||||
| chr12:67271210 | G | C | 8 | a0001c0001t0008g0032 a0001c0001t0008g0033 a0001c0001t0008g0034 others(5): Show |
10 | HG00597.hp2 NA18941.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+1425G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271210 | |||||||
| chr12:67271319 | A | G | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+1534A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271319 | |||||||
| chr12:67271500 | G | T | 3 | a0001c0002t0001g0140 a0001c0002t0001g0141 a0001c0002t0001g0142 |
3 | HG00738.hp1 HG01517.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.68+1715G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271500 | |||||||
| chr12:67271560 | C | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.68+1775C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271560 | |||||||
| chr12:67271676 | G | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.68+1891G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271676 | |||||||
| chr12:67271782 | G | A | 1 | a0001c0001t0061g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.68+1997G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67271782 | |||||||
| chr12:67272022 | A | T | 1 | a0001c0001t0013g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.68+2237A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272022 | |||||||
| chr12:67272055 | A | G | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+2270A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272055 | |||||||
| chr12:67272109 | G | C | 1 | a0001c0002t0054g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.68+2324G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272109 | |||||||
| chr12:67272188 | G | T | 5 | a0001c0004t0014g0019 a0001c0004t0014g0074 a0001c0004t0014g0075 others(2): Show |
6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+2403G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272188 | |||||||
| chr12:67272461 | GAAAT | G | 3 | a0001c0001t0003g0015 a0001c0001t0003g0162 a0001c0001t0025g0163 |
5 | HG02004.hp2 HG02148.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+2677_68+2680del others(4): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272461 | |||||||
| chr12:67272524 | T | G | 2 | a0001c0001t0032g0043 a0001c0001t0034g0042 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.68+2739T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272524 | |||||||
| chr12:67272551 | G | A | 1 | a0001c0002t0001g0024 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.68+2766G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272551 | |||||||
| chr12:67272551 | G | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.68+2766G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272551 | |||||||
| chr12:67272604 | A | G | 1 | a0001c0001t0015g0036 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68+2819A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272604 | |||||||
| chr12:67272721 | T | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.68+2936T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272721 | |||||||
| chr12:67272722 | G | A | 3 | a0001c0005t0029g0080 a0001c0005t0029g0081 a0001c0005t0064g0079 |
3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68+2937G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272722 | |||||||
| chr12:67272757 | C | T | 1 | a0001c0001t0021g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.68+2972C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272757 | |||||||
| chr12:67272941 | C | T | 18 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(15): Show |
23 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.68+3156C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272941 | |||||||
| chr12:67272942 | G | A | 1 | a0001c0005t0064g0079 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68+3157G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67272942 | |||||||
| chr12:67273000 | T | A | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+3215T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273000 | |||||||
| chr12:67273111 | C | T | 1 | a0001c0002t0001g0030 | 2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.68+3326C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273111 | |||||||
| chr12:67273205 | T | C | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.68+3420T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273205 | |||||||
| chr12:67273270 | A | G | 1 | a0001c0002t0055g0139 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.68+3485A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273270 | |||||||
| chr12:67273278 | A | G | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.68+3493A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273278 | |||||||
| chr12:67273284 | G | T | 16 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(13): Show |
23 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.68+3499G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273284 | |||||||
| chr12:67273423 | C | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.68+3638C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273423 | |||||||
| chr12:67273479 | C | CT | 65 | a0001c0001t0015g0197 a0001c0001t0020g0022 a0001c0001t0020g0037 others(62): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.68+3712dupT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67273479 | ||||||
| chr12:67273479 | CT | C | 9 | a0001c0001t0002g0178 a0001c0001t0003g0147 a0001c0001t0003g0162 others(6): Show |
10 | HG01169.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+3712delT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67273479 | ||||||
| chr12:67273524 | A | T | 2 | a0001c0001t0022g0194 a0001c0001t0022g0195 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.68+3739A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273524 | |||||||
| chr12:67273588 | T | G | 1 | a0001c0001t0005g0017 | 2 | HG03491.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.68+3803T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273588 | |||||||
| chr12:67273674 | A | G | 2 | a0001c0001t0028g0065 a0001c0001t0028g0066 |
2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.68+3889A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273674 | |||||||
| chr12:67273704 | T | C | 1 | a0001c0001t0011g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.68+3919T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273704 | |||||||
| chr12:67273951 | C | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.68+4166C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67273951 | |||||||
| chr12:67274047 | C | T | 8 | a0001c0001t0008g0032 a0001c0001t0008g0033 a0001c0001t0008g0034 others(5): Show |
10 | HG00597.hp2 NA18941.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+4262C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274047 | |||||||
| chr12:67274102 | T | G | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.68+4317T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274102 | |||||||
| chr12:67274171 | G | A | 1 | a0001c0002t0009g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68+4386G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274171 | |||||||
| chr12:67274218 | G | A | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.68+4433G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274218 | |||||||
| chr12:67274230 | C | A | 6 | a0001c0001t0012g0005 a0001c0001t0012g0060 a0001c0001t0036g0005 others(3): Show |
10 | HG01361.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+4445C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274230 | |||||||
| chr12:67274231 | C | G | 6 | a0001c0001t0012g0005 a0001c0001t0012g0060 a0001c0001t0036g0005 others(3): Show |
10 | HG01361.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+4446C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274231 | |||||||
| chr12:67274264 | A | G | 1 | a0001c0001t0021g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.68+4479A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274264 | |||||||
| chr12:67274317 | G | C | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.68+4532G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274317 | |||||||
| chr12:67274418 | C | T | 5 | a0001c0004t0014g0019 a0001c0004t0014g0074 a0001c0004t0014g0075 others(2): Show |
6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+4633C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274418 | |||||||
| chr12:67274527 | C | T | 5 | a0001c0004t0014g0019 a0001c0004t0014g0074 a0001c0004t0014g0075 others(2): Show |
6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+4742C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274527 | |||||||
| chr12:67274584 | G | T | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.68+4799G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274584 | |||||||
| chr12:67274698 | C | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0137 a0001c0002t0001g0138 |
4 | HG01168.hp1 HG01169.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+4913C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274698 | |||||||
| chr12:67274820 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68+5035A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274820 | |||||||
| chr12:67274920 | C | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0178 a0001c0001t0002g0192 |
6 | HG03927.hp1 NA18945.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+5135C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67274920 | |||||||
| chr12:67275247 | T | C | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.68+5462T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67275247 | |||||||
| chr12:67275321 | G | T | 1 | a0001c0001t0031g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.68+5536G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67275321 | |||||||
| chr12:67275429 | A | AGGCAGC | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.68+5645_68+5650dup others(6): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67275429 | ||||||
| chr12:67275474 | A | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.68+5689A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67275474 | |||||||
| chr12:67275712 | G | A | 2 | a0001c0001t0004g0168 a0001c0001t0024g0167 |
2 | NA18952.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.68+5927G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67275712 | |||||||
| chr12:67275754 | A | G | 5 | a0001c0004t0014g0019 a0001c0004t0014g0074 a0001c0004t0014g0075 others(2): Show |
6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+5969A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67275754 | |||||||
| chr12:67275888 | A | G | 1 | a0001c0001t0013g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.69-6022A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67275888 | |||||||
| chr12:67275947 | C | T | 2 | a0001c0001t0028g0065 a0001c0001t0028g0066 |
2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69-5963C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67275947 | |||||||
| chr12:67275992 | A | G | 1 | a0001c0009t0001g0136 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.69-5918A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67275992 | |||||||
| chr12:67276016 | A | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.69-5894A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276016 | |||||||
| chr12:67276062 | A | G | 1 | a0001c0001t0045g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.69-5848A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276062 | |||||||
| chr12:67276179 | A | G | 1 | a0001c0001t0004g0177 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.69-5731A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276179 | |||||||
| chr12:67276261 | C | T | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.69-5649C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276261 | |||||||
| chr12:67276325 | G | A | 13 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(10): Show |
17 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.69-5585G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276325 | |||||||
| chr12:67276384 | C | T | 3 | a0001c0005t0029g0080 a0001c0005t0029g0081 a0001c0005t0064g0079 |
3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.69-5526C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276384 | |||||||
| chr12:67276463 | T | G | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.69-5447T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276463 | |||||||
| chr12:67276750 | C | T | 65 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(62): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.69-5160C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276750 | |||||||
| chr12:67276751 | G | A | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.69-5159G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276751 | |||||||
| chr12:67276886 | G | T | 2 | a0001c0001t0018g0023 a0001c0001t0018g0098 |
3 | HG01891.hp1 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.69-5024G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276886 | |||||||
| chr12:67276897 | C | A | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69-5013C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276897 | |||||||
| chr12:67276927 | A | G | 4 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(1): Show |
4 | HG02717.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-4983A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276927 | |||||||
| chr12:67276938 | CATTCCAT others(2164): Show |
C | 1 | a0001c0001t0023g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69-4971_69-2801del | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67276938 | |||||||
| chr12:67277287 | C | A | 147 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(144): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.69-4623C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67277287 | |||||||
| chr12:67277412 | G | A | 2 | a0001c0001t0028g0065 a0001c0001t0028g0066 |
2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69-4498G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67277412 | |||||||
| chr12:67277766 | C | T | 1 | a0001c0001t0017g0045 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.69-4144C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67277766 | |||||||
| chr12:67277802 | A | T | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69-4108A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67277802 | |||||||
| chr12:67277886 | G | T | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.69-4024G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67277886 | |||||||
| chr12:67277890 | CCATT | C | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-4017_69-4014del others(4): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67277890 | ||||||
| chr12:67277979 | C | T | 64 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(61): Show |
81 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.69-3931C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67277979 | |||||||
| chr12:67278109 | C | T | 147 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(144): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.69-3801C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278109 | |||||||
| chr12:67278146 | T | C | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.69-3764T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278146 | |||||||
| chr12:67278246 | C | T | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.69-3664C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278246 | |||||||
| chr12:67278381 | T | C | 9 | a0001c0001t0007g0090 a0001c0001t0007g0092 a0001c0001t0007g0093 others(6): Show |
10 | HG01069.hp2 HG01261.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-3529T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278381 | |||||||
| chr12:67278572 | G | A | 1 | a0001c0002t0001g0001 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.69-3338G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278572 | |||||||
| chr12:67278578 | G | A | 4 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(1): Show |
4 | HG02717.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-3332G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278578 | |||||||
| chr12:67278817 | G | T | 2 | a0001c0002t0001g0007 a0001c0002t0001g0104 |
2 | NA18955.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.69-3093G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278817 | |||||||
| chr12:67278898 | G | T | 1 | a0001c0001t0032g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.69-3012G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278898 | |||||||
| chr12:67278910 | G | A | 9 | a0001c0001t0021g0021 a0001c0001t0021g0089 a0001c0003t0010g0020 others(6): Show |
11 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-3000G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67278910 | |||||||
| chr12:67279011 | G | C | 3 | a0001c0001t0028g0065 a0001c0001t0028g0066 a0001c0001t0045g0067 |
3 | HG01109.hp1 HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69-2899G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279011 | |||||||
| chr12:67279045 | G | T | 19 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(16): Show |
24 | HG01069.hp2 HG01261.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.69-2865G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279045 | |||||||
| chr12:67279049 | A | T | 9 | a0001c0001t0021g0021 a0001c0001t0021g0089 a0001c0003t0010g0020 others(6): Show |
11 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-2861A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279049 | |||||||
| chr12:67279090 | A | G | 9 | a0001c0002t0001g0010 a0001c0002t0001g0030 a0001c0002t0001g0129 others(6): Show |
12 | HG00140.hp1 HG00733.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-2820A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279090 | |||||||
| chr12:67279098 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.69-2812A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279098 | |||||||
| chr12:67279111 | G | T | 1 | a0001c0001t0023g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69-2799G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279111 | |||||||
| chr12:67279112 | C | G | 1 | a0001c0001t0023g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69-2798C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279112 | |||||||
| chr12:67279117 | C | G | 1 | a0001c0001t0023g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69-2793C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279117 | |||||||
| chr12:67279119 | T | G | 1 | a0001c0001t0023g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69-2791T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279119 | |||||||
| chr12:67279120 | A | T | 1 | a0001c0001t0023g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69-2790A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279120 | |||||||
| chr12:67279123 | G | T | 1 | a0001c0001t0023g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69-2787G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279123 | |||||||
| chr12:67279125 | A | G | 12 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(9): Show |
16 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.69-2785A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279125 | |||||||
| chr12:67279174 | C | CA | 141 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(138): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.69-2720dupA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67279174 | ||||||
| chr12:67279174 | CA | C | 4 | a0001c0001t0002g0191 a0001c0001t0003g0014 a0001c0001t0003g0196 others(1): Show |
6 | HG01168.hp2 HG03688.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.69-2720delA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67279174 | ||||||
| chr12:67279392 | C | G | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.69-2518C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279392 | |||||||
| chr12:67279599 | T | A | 19 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(16): Show |
26 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.69-2311T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279599 | |||||||
| chr12:67279739 | G | C | 4 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-2171G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279739 | |||||||
| chr12:67279818 | T | G | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69-2092T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279818 | |||||||
| chr12:67279872 | G | A | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.69-2038G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67279872 | |||||||
| chr12:67280124 | G | A | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.69-1786G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280124 | |||||||
| chr12:67280149 | T | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.69-1761T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280149 | |||||||
| chr12:67280200 | A | G | 41 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(38): Show |
53 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.69-1710A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280200 | |||||||
| chr12:67280211 | A | G | 10 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(7): Show |
14 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.69-1699A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280211 | |||||||
| chr12:67280415 | C | T | 3 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0001g0144 |
3 | HG02004.hp1 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.69-1495C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280415 | |||||||
| chr12:67280431 | A | G | 1 | a0001c0002t0009g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69-1479A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280431 | |||||||
| chr12:67280432 | T | G | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-1478T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280432 | |||||||
| chr12:67280619 | A | G | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.69-1291A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280619 | |||||||
| chr12:67280844 | AC | A | 12 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(9): Show |
16 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.69-1065delC | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280844 | |||||||
| chr12:67280881 | G | T | 12 | a0001c0001t0021g0021 a0001c0001t0021g0089 a0001c0003t0010g0020 others(9): Show |
14 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-1029G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280881 | |||||||
| chr12:67280895 | C | A | 171 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0170 others(168): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.69-1015C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280895 | |||||||
| chr12:67280965 | G | T | 2 | a0001c0004t0014g0077 a0001c0004t0047g0076 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.69-945G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67280965 | |||||||
| chr12:67281057 | A | G | 5 | a0001c0004t0014g0019 a0001c0004t0014g0074 a0001c0004t0014g0075 others(2): Show |
6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.69-853A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67281057 | |||||||
| chr12:67281166 | C | T | 19 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(16): Show |
26 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.69-744C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67281166 | |||||||
| chr12:67281336 | AAAG | A | 6 | a0001c0001t0012g0005 a0001c0001t0012g0060 a0001c0001t0036g0005 others(3): Show |
10 | HG01361.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-572_69-570delAG others(1): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 67281336 | ||||||
| chr12:67281385 | G | T | 6 | a0001c0001t0012g0005 a0001c0001t0012g0060 a0001c0001t0036g0005 others(3): Show |
10 | HG01361.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-525G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67281385 | |||||||
| chr12:67281447 | C | T | 1 | a0001c0001t0007g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.69-463C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67281447 | |||||||
| chr12:67281499 | G | A | 2 | a0001c0001t0003g0148 a0001c0001t0003g0149 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.69-411G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67281499 | |||||||
| chr12:67281581 | G | A | 65 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(62): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.69-329G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67281581 | |||||||
| chr12:67281708 | A | G | 1 | a0001c0002t0053g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.69-202A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 1/14 | chr12 | 67281708 | |||||||
| chr12:67282268 | A | G | 1 | a0001c0001t0017g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.212+215A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282268 | |||||||
| chr12:67282297 | A | C | 1 | a0001c0001t0003g0196 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.212+244A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282297 | |||||||
| chr12:67282343 | GTTGAGTT others(10): Show |
G | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.212+293_212+309del others(17): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67282343 | ||||||
| chr12:67282415 | C | T | 132 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(129): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.212+362C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282415 | |||||||
| chr12:67282523 | C | T | 3 | a0001c0005t0029g0080 a0001c0005t0029g0081 a0001c0005t0064g0079 |
3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212+470C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282523 | |||||||
| chr12:67282602 | G | C | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.212+549G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282602 | |||||||
| chr12:67282782 | A | G | 2 | a0001c0001t0004g0146 a0001c0001t0044g0176 |
2 | HG00140.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.212+729A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282782 | |||||||
| chr12:67282796 | C | T | 2 | a0001c0001t0013g0072 a0001c0001t0013g0078 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.212+743C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282796 | |||||||
| chr12:67282817 | G | T | 1 | a0001c0002t0016g0135 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.212+764G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282817 | |||||||
| chr12:67282838 | G | C | 2 | a0001c0001t0028g0065 a0001c0001t0028g0066 |
2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.212+785G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282838 | |||||||
| chr12:67282862 | T | C | 19 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(16): Show |
26 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.212+809T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67282862 | |||||||
| chr12:67283034 | C | G | 1 | a0001c0001t0027g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.212+981C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283034 | |||||||
| chr12:67283329 | A | G | 37 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(34): Show |
49 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.212+1276A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283329 | |||||||
| chr12:67283371 | G | A | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+1318G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283371 | |||||||
| chr12:67283386 | C | A | 1 | a0001c0002t0001g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.212+1333C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283386 | |||||||
| chr12:67283437 | G | T | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+1384G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283437 | |||||||
| chr12:67283442 | G | A | 10 | a0001c0001t0007g0090 a0001c0001t0007g0092 a0001c0001t0007g0093 others(7): Show |
11 | HG01069.hp2 HG01261.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.212+1389G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283442 | |||||||
| chr12:67283537 | C | T | 1 | a0001c0002t0001g0013 | 3 | NA18962.hp1 NA19004.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.212+1484C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283537 | |||||||
| chr12:67283561 | C | T | 4 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+1508C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283561 | |||||||
| chr12:67283582 | C | CA | 38 | a0001c0001t0004g0150 a0001c0001t0006g0051 a0001c0001t0007g0061 others(35): Show |
45 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.212+1545dupA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67283582 | ||||||
| chr12:67283621 | C | G | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.212+1568C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283621 | |||||||
| chr12:67283647 | T | C | 1 | a0001c0001t0008g0164 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.212+1594T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283647 | |||||||
| chr12:67283811 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.212+1758T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283811 | |||||||
| chr12:67283814 | A | G | 1 | a0001c0001t0006g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.212+1761A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283814 | |||||||
| chr12:67283856 | A | G | 65 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(62): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.212+1803A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283856 | |||||||
| chr12:67283935 | A | G | 4 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(1): Show |
4 | HG02717.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+1882A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283935 | |||||||
| chr12:67283966 | T | C | 1 | a0001c0001t0028g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.212+1913T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67283966 | |||||||
| chr12:67284337 | A | G | 41 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(38): Show |
53 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.212+2284A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67284337 | |||||||
| chr12:67284371 | AT | A | 37 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(34): Show |
49 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.212+2322delT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67284371 | ||||||
| chr12:67284432 | A | C | 1 | a0001c0001t0005g0057 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.212+2379A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67284432 | |||||||
| chr12:67284461 | C | G | 1 | a0001c0001t0022g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212+2408C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67284461 | |||||||
| chr12:67284705 | T | TAC | 38 | a0001c0001t0007g0062 a0001c0001t0007g0090 a0001c0001t0007g0092 others(35): Show |
45 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.212+2672_212+2673d others(4): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67284705 | ||||||
| chr12:67284705 | T | TACAC | 4 | a0001c0001t0003g0035 a0001c0001t0037g0063 a0001c0001t0041g0035 others(1): Show |
4 | HG00733.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.212+2670_212+2673d others(6): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67284705 | ||||||
| chr12:67284711 | C | CACACACA others(74): Show |
1 | a0001c0002t0001g0103 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.212+2671_212+2672i others(83): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67284711 | ||||||
| chr12:67284711 | C | CACACACA others(76): Show |
10 | a0001c0001t0062g0145 a0001c0002t0001g0007 a0001c0002t0001g0013 others(7): Show |
17 | HG02523.hp2 HG02683.hp2 HG03471.hp2 others(14): Show |
intron_variant | MODIFIER | c.212+2667_212+2749d others(85): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67284711 | ||||||
| chr12:67284711 | C | CACACACA others(78): Show |
55 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(52): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.212+2673_212+2674i others(87): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67284711 | ||||||
| chr12:67284711 | C | CACACACA others(78): Show |
1 | a0001c0002t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.212+2673_212+2674i others(87): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67284711 | ||||||
| chr12:67284725 | CAA | C | 16 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(13): Show |
23 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.212+2674_212+2675d others(4): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67284725 | ||||||
| chr12:67284794 | T | C | 5 | a0001c0001t0006g0052 a0001c0001t0007g0061 a0001c0001t0007g0062 others(2): Show |
5 | HG02155.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+2741T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67284794 | |||||||
| chr12:67284860 | A | G | 1 | a0001c0001t0019g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.212+2807A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67284860 | |||||||
| chr12:67284952 | G | T | 1 | a0001c0002t0001g0134 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.212+2899G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67284952 | |||||||
| chr12:67284959 | T | A | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.212+2906T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67284959 | |||||||
| chr12:67285082 | G | C | 3 | a0001c0001t0028g0065 a0001c0001t0028g0066 a0001c0001t0045g0067 |
3 | HG01109.hp1 HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.212+3029G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67285082 | |||||||
| chr12:67285179 | C | G | 2 | a0001c0001t0032g0043 a0001c0001t0034g0042 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.212+3126C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67285179 | |||||||
| chr12:67285262 | C | G | 1 | a0001c0002t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.212+3209C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67285262 | |||||||
| chr12:67285725 | G | A | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.212+3672G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67285725 | |||||||
| chr12:67285800 | T | A | 3 | a0001c0002t0001g0009 a0001c0002t0001g0024 a0001c0002t0001g0027 |
8 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+3747T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67285800 | |||||||
| chr12:67285992 | T | C | 9 | a0001c0001t0021g0021 a0001c0001t0021g0089 a0001c0003t0010g0020 others(6): Show |
11 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.212+3939T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67285992 | |||||||
| chr12:67286009 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.212+3956A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286009 | |||||||
| chr12:67286044 | G | C | 65 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(62): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.212+3991G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286044 | |||||||
| chr12:67286094 | G | A | 1 | a0001c0001t0005g0057 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.212+4041G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286094 | |||||||
| chr12:67286120 | G | C | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+4067G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286120 | |||||||
| chr12:67286231 | C | T | 2 | a0001c0001t0007g0090 a0001c0001t0007g0095 |
2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.212+4178C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286231 | |||||||
| chr12:67286271 | A | G | 1 | a0001c0004t0014g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.212+4218A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286271 | |||||||
| chr12:67286285 | C | T | 1 | a0001c0001t0031g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.212+4232C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286285 | |||||||
| chr12:67286395 | C | G | 1 | a0001c0001t0017g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.212+4342C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286395 | |||||||
| chr12:67286454 | G | A | 1 | a0001c0001t0033g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.212+4401G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286454 | |||||||
| chr12:67286538 | A | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.212+4485A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286538 | |||||||
| chr12:67286562 | A | AT | 82 | a0001c0001t0012g0005 a0001c0001t0012g0060 a0001c0001t0021g0021 others(79): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.212+4522dupT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67286562 | ||||||
| chr12:67286562 | A | ATT | 9 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(6): Show |
9 | HG00099.hp2 HG01261.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.212+4521_212+4522d others(4): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67286562 | ||||||
| chr12:67286605 | GTTC | G | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+4557_212+4559d others(5): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67286605 | ||||||
| chr12:67286799 | C | T | 1 | a0001c0001t0008g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.212+4746C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286799 | |||||||
| chr12:67286885 | A | T | 2 | a0001c0001t0007g0093 a0001c0001t0007g0094 |
2 | HG01069.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.212+4832A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67286885 | |||||||
| chr12:67287051 | A | G | 10 | a0001c0002t0001g0010 a0001c0002t0001g0030 a0001c0002t0001g0129 others(7): Show |
13 | HG00140.hp1 HG00733.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.212+4998A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287051 | |||||||
| chr12:67287077 | T | C | 2 | a0001c0001t0003g0035 a0001c0001t0041g0035 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.212+5024T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287077 | |||||||
| chr12:67287289 | C | T | 1 | a0001c0001t0045g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.212+5236C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287289 | |||||||
| chr12:67287325 | G | A | 1 | a0001c0001t0003g0031 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.212+5272G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287325 | |||||||
| chr12:67287380 | A | G | 7 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(4): Show |
10 | HG02145.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.213-5242A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287380 | |||||||
| chr12:67287612 | T | C | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.213-5010T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287612 | |||||||
| chr12:67287645 | G | A | 23 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(20): Show |
30 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.213-4977G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287645 | |||||||
| chr12:67287737 | G | C | 147 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(144): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.213-4885G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287737 | |||||||
| chr12:67287784 | A | G | 2 | a0001c0001t0021g0021 a0001c0001t0021g0089 |
3 | HG03139.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.213-4838A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287784 | |||||||
| chr12:67287797 | C | T | 1 | a0001c0001t0045g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.213-4825C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287797 | |||||||
| chr12:67287803 | A | G | 1 | a0001c0001t0028g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.213-4819A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287803 | |||||||
| chr12:67287857 | A | AT | 109 | a0001c0001t0002g0170 a0001c0001t0002g0179 a0001c0001t0002g0186 others(106): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.213-4744dupT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67287857 | ||||||
| chr12:67287857 | A | ATT | 16 | a0001c0001t0002g0189 a0001c0001t0004g0011 a0001c0001t0004g0150 others(13): Show |
20 | HG01928.hp1 HG01975.hp2 HG02273.hp1 others(17): Show |
intron_variant | MODIFIER | c.213-4745_213-4744d others(4): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67287857 | ||||||
| chr12:67287857 | AT | A | 53 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(50): Show |
66 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.213-4744delT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67287857 | ||||||
| chr12:67287857 | ATT | A | 7 | a0001c0001t0012g0005 a0001c0001t0018g0023 a0001c0001t0036g0005 others(4): Show |
12 | HG01069.hp1 HG01361.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.213-4745_213-4744d others(4): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67287857 | ||||||
| chr12:67287923 | A | T | 1 | a0001c0002t0001g0142 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.213-4699A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67287923 | |||||||
| chr12:67288124 | T | G | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.213-4498T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288124 | |||||||
| chr12:67288136 | A | AT | 7 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(4): Show |
7 | HG02717.hp1 HG02738.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.213-4467dupT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67288136 | ||||||
| chr12:67288136 | AT | A | 25 | a0001c0001t0002g0191 a0001c0001t0007g0061 a0001c0001t0007g0062 others(22): Show |
30 | HG01069.hp2 HG01261.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.213-4467delT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67288136 | ||||||
| chr12:67288155 | T | A | 1 | a0001c0001t0013g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.213-4467T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288155 | |||||||
| chr12:67288273 | C | T | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.213-4349C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288273 | |||||||
| chr12:67288288 | T | C | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.213-4334T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288288 | |||||||
| chr12:67288316 | C | T | 37 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(34): Show |
49 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.213-4306C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288316 | |||||||
| chr12:67288347 | C | T | 20 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(17): Show |
25 | HG01069.hp2 HG01261.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.213-4275C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288347 | |||||||
| chr12:67288615 | A | G | 1 | a0001c0003t0010g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.213-4007A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288615 | |||||||
| chr12:67288636 | A | G | 1 | a0001c0001t0028g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.213-3986A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288636 | |||||||
| chr12:67288751 | C | A | 1 | a0001c0001t0007g0093 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.213-3871C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288751 | |||||||
| chr12:67288771 | C | A | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.213-3851C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288771 | |||||||
| chr12:67288784 | A | G | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.213-3838A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288784 | |||||||
| chr12:67288838 | G | A | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.213-3784G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67288838 | |||||||
| chr12:67289060 | ATCT | A | 2 | a0001c0001t0021g0021 a0001c0001t0021g0089 |
3 | HG03139.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.213-3557_213-3555d others(5): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67289060 | ||||||
| chr12:67289181 | T | C | 1 | a0001c0001t0025g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.213-3441T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67289181 | |||||||
| chr12:67289280 | G | A | 2 | a0001c0001t0032g0043 a0001c0001t0034g0042 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.213-3342G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67289280 | |||||||
| chr12:67289367 | T | TACC | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.213-3253_213-3251d others(5): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67289367 | ||||||
| chr12:67289432 | A | G | 1 | a0001c0001t0007g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.213-3190A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67289432 | |||||||
| chr12:67289466 | G | T | 1 | a0001c0001t0004g0190 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.213-3156G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67289466 | |||||||
| chr12:67289850 | T | G | 1 | a0001c0002t0001g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.213-2772T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67289850 | |||||||
| chr12:67289883 | T | C | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.213-2739T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67289883 | |||||||
| chr12:67289908 | G | A | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.213-2714G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67289908 | |||||||
| chr12:67289945 | T | C | 1 | a0001c0001t0025g0163 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.213-2677T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67289945 | |||||||
| chr12:67290165 | C | T | 18 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(15): Show |
23 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.213-2457C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290165 | |||||||
| chr12:67290256 | A | G | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.213-2366A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290256 | |||||||
| chr12:67290283 | G | A | 3 | a0001c0005t0029g0080 a0001c0005t0029g0081 a0001c0005t0064g0079 |
3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.213-2339G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290283 | |||||||
| chr12:67290339 | C | T | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.213-2283C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290339 | |||||||
| chr12:67290383 | T | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.213-2239T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290383 | |||||||
| chr12:67290487 | G | C | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.213-2135G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290487 | |||||||
| chr12:67290655 | T | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.213-1967T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290655 | |||||||
| chr12:67290657 | G | T | 1 | a0001c0001t0003g0174 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.213-1965G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290657 | |||||||
| chr12:67290690 | T | A | 1 | a0001c0002t0001g0117 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.213-1932T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290690 | |||||||
| chr12:67290701 | G | A | 1 | a0001c0001t0003g0153 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.213-1921G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290701 | |||||||
| chr12:67290756 | A | G | 2 | a0001c0001t0004g0146 a0001c0001t0044g0176 |
2 | HG00140.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.213-1866A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290756 | |||||||
| chr12:67290779 | T | C | 1 | a0001c0001t0020g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.213-1843T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290779 | |||||||
| chr12:67290875 | G | A | 19 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(16): Show |
26 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.213-1747G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290875 | |||||||
| chr12:67290922 | T | C | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.213-1700T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67290922 | |||||||
| chr12:67291358 | TCTC | T | 2 | a0001c0001t0021g0021 a0001c0001t0021g0089 |
3 | HG03139.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.213-1260_213-1258d others(5): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 67291358 | ||||||
| chr12:67291558 | G | A | 1 | a0001c0002t0009g0118 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.213-1064G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67291558 | |||||||
| chr12:67291623 | C | A | 1 | a0001c0001t0002g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.213-999C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67291623 | |||||||
| chr12:67291702 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.213-920G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67291702 | |||||||
| chr12:67291723 | A | T | 1 | a0001c0001t0020g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.213-899A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67291723 | |||||||
| chr12:67291783 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.213-839G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67291783 | |||||||
| chr12:67291813 | G | T | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.213-809G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67291813 | |||||||
| chr12:67291863 | G | A | 1 | a0001c0002t0001g0110 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.213-759G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67291863 | |||||||
| chr12:67292002 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.213-620C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292002 | |||||||
| chr12:67292019 | T | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.213-603T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292019 | |||||||
| chr12:67292055 | C | T | 1 | a0001c0002t0001g0105 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.213-567C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292055 | |||||||
| chr12:67292084 | C | T | 1 | a0001c0001t0013g0018 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.213-538C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292084 | |||||||
| chr12:67292092 | C | T | 18 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(15): Show |
23 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.213-530C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292092 | |||||||
| chr12:67292127 | G | A | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.213-495G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292127 | |||||||
| chr12:67292163 | G | A | 27 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(24): Show |
32 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.213-459G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292163 | |||||||
| chr12:67292314 | T | A | 1 | a0003c0006t0002g0180 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.213-308T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292314 | |||||||
| chr12:67292314 | T | C | 1 | a0001c0005t0029g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.213-308T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292314 | |||||||
| chr12:67292386 | G | A | 65 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(62): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.213-236G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292386 | |||||||
| chr12:67292447 | A | G | 1 | a0001c0011t0001g0099 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.213-175A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292447 | |||||||
| chr12:67292452 | T | C | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.213-170T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292452 | |||||||
| chr12:67292466 | A | C | 1 | a0001c0004t0014g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.213-156A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292466 | |||||||
| chr12:67292508 | G | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0137 a0001c0002t0001g0138 |
4 | HG01168.hp1 HG01169.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-114G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292508 | |||||||
| chr12:67292577 | G | C | 4 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-45G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 2/14 | chr12 | 67292577 | |||||||
| chr12:67292811 | T | A | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+35T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67292811 | |||||||
| chr12:67292882 | C | G | 1 | a0001c0002t0001g0131 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.367+106C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67292882 | |||||||
| chr12:67293152 | G | A | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.367+376G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67293152 | |||||||
| chr12:67293352 | G | A | 1 | a0001c0001t0006g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.367+576G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67293352 | |||||||
| chr12:67293411 | A | G | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.367+635A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67293411 | |||||||
| chr12:67293716 | G | A | 1 | a0001c0002t0001g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.367+940G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67293716 | |||||||
| chr12:67293748 | C | T | 1 | a0001c0001t0005g0050 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.367+972C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67293748 | |||||||
| chr12:67293791 | T | C | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.367+1015T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67293791 | |||||||
| chr12:67293859 | A | G | 1 | a0001c0002t0001g0110 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.367+1083A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67293859 | |||||||
| chr12:67294012 | G | C | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.368-1021G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67294012 | |||||||
| chr12:67294265 | C | G | 4 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(1): Show |
7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-768C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67294265 | |||||||
| chr12:67294329 | C | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.368-704C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67294329 | |||||||
| chr12:67294348 | C | T | 3 | a0001c0001t0020g0022 a0001c0001t0020g0088 a0001c0001t0065g0022 |
3 | HG02717.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.368-685C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67294348 | |||||||
| chr12:67294392 | AT | A | 13 | a0001c0001t0021g0021 a0001c0001t0021g0089 a0001c0002t0001g0117 others(10): Show |
15 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.368-630delT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 67294392 | ||||||
| chr12:67294560 | C | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.368-473C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67294560 | |||||||
| chr12:67294633 | A | G | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.368-400A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67294633 | |||||||
| chr12:67294783 | T | C | 1 | a0001c0001t0005g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.368-250T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67294783 | |||||||
| chr12:67294938 | G | A | 65 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(62): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.368-95G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 3/14 | chr12 | 67294938 | |||||||
| chr12:67295178 | C | T | 7 | a0001c0003t0010g0020 a0001c0003t0010g0084 a0001c0003t0010g0085 others(4): Show |
8 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.491+22C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67295178 | |||||||
| chr12:67295528 | C | T | 3 | a0001c0001t0028g0065 a0001c0001t0028g0066 a0001c0001t0045g0067 |
3 | HG01109.hp1 HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.491+372C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67295528 | |||||||
| chr12:67295529 | G | A | 10 | a0001c0001t0007g0090 a0001c0001t0007g0092 a0001c0001t0007g0093 others(7): Show |
11 | HG01069.hp2 HG01261.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.491+373G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67295529 | |||||||
| chr12:67295614 | T | A | 2 | a0001c0001t0028g0065 a0001c0001t0028g0066 |
2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.491+458T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67295614 | |||||||
| chr12:67295637 | C | T | 1 | a0001c0001t0003g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.491+481C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67295637 | |||||||
| chr12:67295694 | A | G | 1 | a0001c0002t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.491+538A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67295694 | |||||||
| chr12:67296006 | T | G | 1 | a0003c0006t0002g0180 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.491+850T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296006 | |||||||
| chr12:67296115 | G | T | 13 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(10): Show |
17 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.491+959G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296115 | |||||||
| chr12:67296147 | TA | T | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.491+992delA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296147 | |||||||
| chr12:67296196 | A | G | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.491+1040A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296196 | |||||||
| chr12:67296260 | A | G | 1 | a0001c0001t0020g0088 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.491+1104A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296260 | |||||||
| chr12:67296419 | A | C | 1 | a0001c0002t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.492-988A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296419 | |||||||
| chr12:67296652 | C | G | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.492-755C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296652 | |||||||
| chr12:67296655 | G | A | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.492-752G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296655 | |||||||
| chr12:67296705 | G | A | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.492-702G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67296705 | |||||||
| chr12:67296747 | T | TA | 6 | a0001c0003t0010g0020 a0001c0003t0010g0084 a0001c0003t0010g0085 others(3): Show |
7 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.492-659dupA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 67296747 | ||||||
| chr12:67297003 | G | T | 8 | a0001c0001t0007g0092 a0001c0001t0007g0093 a0001c0001t0007g0094 others(5): Show |
9 | HG01069.hp2 HG01261.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.492-404G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67297003 | |||||||
| chr12:67297139 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.492-268A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67297139 | |||||||
| chr12:67297188 | C | G | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-219C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 4/14 | chr12 | 67297188 | |||||||
| chr12:67297673 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.748+10C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 5/14 | chr12 | 67297673 | |||||||
| chr12:67297678 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.748+15A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 5/14 | chr12 | 67297678 | |||||||
| chr12:67298144 | G | T | 1 | a0001c0001t0003g0162 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.854+291G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | chr12 | 67298144 | |||||||
| chr12:67298271 | A | G | 1 | a0001c0011t0001g0099 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.854+418A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | chr12 | 67298271 | |||||||
| chr12:67298365 | A | ATG | 65 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(62): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.854+513_854+514dup others(2): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 67298365 | ||||||
| chr12:67298370 | G | T | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.854+517G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | chr12 | 67298370 | |||||||
| chr12:67298454 | T | C | 1 | a0001c0001t0003g0172 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.855-496T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | chr12 | 67298454 | |||||||
| chr12:67298536 | C | T | 1 | a0001c0001t0013g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.855-414C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | chr12 | 67298536 | |||||||
| chr12:67298563 | A | G | 18 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(15): Show |
23 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.855-387A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | chr12 | 67298563 | |||||||
| chr12:67298565 | C | T | 10 | a0001c0001t0007g0090 a0001c0001t0007g0092 a0001c0001t0007g0093 others(7): Show |
11 | HG01069.hp2 HG01261.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.855-385C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | chr12 | 67298565 | |||||||
| chr12:67298901 | CAAG | C | 6 | a0001c0001t0012g0005 a0001c0001t0012g0060 a0001c0001t0036g0005 others(3): Show |
10 | HG01361.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.855-48_855-46delAA others(1): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 6/14 | chr12 | 67298901 | |||||||
| chr12:67299138 | C | T | 13 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(10): Show |
17 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1000+43C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67299138 | |||||||
| chr12:67299328 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1000+233T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67299328 | |||||||
| chr12:67299453 | A | G | 2 | a0001c0001t0022g0194 a0001c0001t0022g0195 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1000+358A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67299453 | |||||||
| chr12:67299523 | G | A | 1 | a0001c0001t0006g0055 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1000+428G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67299523 | |||||||
| chr12:67299897 | A | T | 1 | a0001c0001t0011g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1000+802A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67299897 | |||||||
| chr12:67299973 | A | G | 10 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(7): Show |
14 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1000+878A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67299973 | |||||||
| chr12:67300118 | C | G | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1000+1023C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67300118 | |||||||
| chr12:67300252 | G | C | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1000+1157G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67300252 | |||||||
| chr12:67300280 | TA | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0178 others(162): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1000+1187delA | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 67300280 | ||||||
| chr12:67300299 | T | C | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1000+1204T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67300299 | |||||||
| chr12:67300309 | G | C | 1 | a0003c0006t0002g0180 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1000+1214G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67300309 | |||||||
| chr12:67300897 | C | T | 1 | a0001c0001t0045g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1001-1426C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67300897 | |||||||
| chr12:67301368 | C | T | 1 | a0001c0001t0031g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1001-955C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67301368 | |||||||
| chr12:67301553 | C | T | 1 | a0001c0002t0001g0029 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1001-770C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67301553 | |||||||
| chr12:67301556 | C | T | 3 | a0001c0005t0029g0080 a0001c0005t0029g0081 a0001c0005t0064g0079 |
3 | HG01884.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-767C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67301556 | |||||||
| chr12:67301625 | A | G | 1 | a0001c0002t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1001-698A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67301625 | |||||||
| chr12:67301903 | A | G | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-420A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67301903 | |||||||
| chr12:67302023 | G | A | 6 | a0001c0001t0012g0005 a0001c0001t0012g0060 a0001c0001t0036g0005 others(3): Show |
10 | HG01361.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001-300G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67302023 | |||||||
| chr12:67302029 | T | G | 1 | a0001c0001t0045g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1001-294T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67302029 | |||||||
| chr12:67302044 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0028 |
4 | NA18944.hp2 NA18950.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-279G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67302044 | |||||||
| chr12:67302208 | T | A | 1 | a0001c0002t0001g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1001-115T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67302208 | |||||||
| chr12:67302272 | A | T | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1001-51A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 7/14 | chr12 | 67302272 | |||||||
| chr12:67302895 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1293+280A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67302895 | |||||||
| chr12:67302941 | G | C | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1293+326G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67302941 | |||||||
| chr12:67303042 | G | A | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1293+427G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303042 | |||||||
| chr12:67303139 | A | G | 1 | a0001c0001t0003g0147 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1293+524A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303139 | |||||||
| chr12:67303389 | G | A | 24 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(21): Show |
29 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1293+774G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303389 | |||||||
| chr12:67303495 | C | T | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1293+880C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303495 | |||||||
| chr12:67303537 | C | T | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1293+922C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303537 | |||||||
| chr12:67303545 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1293+930T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303545 | |||||||
| chr12:67303592 | G | T | 1 | a0001c0001t0032g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1293+977G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303592 | |||||||
| chr12:67303739 | C | G | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1294-866C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303739 | |||||||
| chr12:67303854 | T | C | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(63): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1294-751T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303854 | |||||||
| chr12:67303938 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1294-667T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303938 | |||||||
| chr12:67303992 | CT | C | 20 | a0001c0001t0006g0040 a0001c0001t0020g0022 a0001c0001t0020g0037 others(17): Show |
22 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1294-597delT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 67303992 | ||||||
| chr12:67303994 | T | C | 1 | a0001c0001t0003g0147 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1294-611T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67303994 | |||||||
| chr12:67304076 | G | A | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1294-529G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67304076 | |||||||
| chr12:67304115 | G | A | 10 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(7): Show |
14 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1294-490G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67304115 | |||||||
| chr12:67304147 | G | A | 1 | a0001c0001t0032g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1294-458G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67304147 | |||||||
| chr12:67304182 | G | T | 1 | a0001c0001t0004g0183 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1294-423G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67304182 | |||||||
| chr12:67304292 | A | C | 1 | a0001c0001t0031g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1294-313A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67304292 | |||||||
| chr12:67304477 | T | G | 4 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(1): Show |
4 | HG02717.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294-128T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67304477 | |||||||
| chr12:67304543 | T | C | 4 | a0001c0001t0017g0044 a0001c0001t0017g0045 a0001c0001t0017g0046 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294-62T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 8/14 | chr12 | 67304543 | |||||||
| chr12:67306618 | A | T | 22 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0146 others(19): Show |
31 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2929+21A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/14 | chr12 | 67306618 | |||||||
| chr12:67306783 | A | T | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2929+186A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/14 | chr12 | 67306783 | |||||||
| chr12:67306852 | A | G | 1 | a0001c0001t0003g0157 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2929+255A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/14 | chr12 | 67306852 | |||||||
| chr12:67307091 | A | T | 1 | a0001c0002t0051g0112 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2930-306A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/14 | chr12 | 67307091 | |||||||
| chr12:67307160 | A | G | 1 | a0001c0005t0064g0079 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2930-237A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/14 | chr12 | 67307160 | |||||||
| chr12:67307323 | G | A | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2930-74G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/14 | chr12 | 67307323 | |||||||
| chr12:67307342 | T | A | 1 | a0001c0001t0007g0093 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2930-55T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/14 | chr12 | 67307342 | |||||||
| chr12:67307371 | T | C | 1 | a0001c0001t0003g0161 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2930-26T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 10/14 | chr12 | 67307371 | |||||||
| chr12:67307594 | T | C | 65 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(62): Show |
82 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.3025+102T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67307594 | |||||||
| chr12:67307659 | A | G | 2 | a0001c0001t0021g0021 a0001c0001t0021g0089 |
3 | HG03139.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3025+167A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67307659 | |||||||
| chr12:67307735 | A | G | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3025+243A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67307735 | |||||||
| chr12:67307921 | T | A | 1 | a0001c0001t0037g0063 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3025+429T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67307921 | |||||||
| chr12:67307960 | G | T | 12 | a0001c0001t0021g0021 a0001c0001t0021g0089 a0001c0003t0010g0020 others(9): Show |
14 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.3025+468G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67307960 | |||||||
| chr12:67307986 | T | C | 10 | a0001c0001t0011g0008 a0001c0001t0011g0069 a0001c0001t0011g0071 others(7): Show |
14 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3025+494T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67307986 | |||||||
| chr12:67308021 | C | G | 3 | a0001c0001t0028g0065 a0001c0001t0028g0066 a0001c0001t0045g0067 |
3 | HG01109.hp1 HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3025+529C>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308021 | |||||||
| chr12:67308078 | T | A | 1 | a0001c0001t0003g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3025+586T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308078 | |||||||
| chr12:67308079 | T | G | 1 | a0001c0001t0003g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3025+587T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308079 | |||||||
| chr12:67308379 | A | T | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3025+887A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308379 | |||||||
| chr12:67308380 | A | T | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3025+888A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308380 | |||||||
| chr12:67308401 | A | C | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.3025+909A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308401 | |||||||
| chr12:67308418 | A | G | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3025+926A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308418 | |||||||
| chr12:67308572 | T | C | 19 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(16): Show |
26 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.3025+1080T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308572 | |||||||
| chr12:67308779 | T | A | 2 | a0001c0001t0004g0146 a0001c0001t0044g0176 |
2 | HG00140.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3026-1122T>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308779 | |||||||
| chr12:67308921 | A | C | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3026-980A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67308921 | |||||||
| chr12:67308946 | CTT | C | 3 | a0001c0001t0028g0065 a0001c0001t0028g0066 a0001c0001t0045g0067 |
3 | HG01109.hp1 HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3026-952_3026-951d others(4): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 67308946 | ||||||
| chr12:67309023 | A | G | 1 | a0001c0002t0001g0133 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3026-878A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309023 | |||||||
| chr12:67309070 | A | G | 1 | a0001c0003t0010g0086 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3026-831A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309070 | |||||||
| chr12:67309074 | A | C | 2 | a0001c0001t0024g0156 a0001c0001t0024g0167 |
2 | NA18994.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.3026-827A>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309074 | |||||||
| chr12:67309078 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3026-823G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309078 | |||||||
| chr12:67309190 | T | C | 1 | a0001c0002t0001g0027 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3026-711T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309190 | |||||||
| chr12:67309272 | A | T | 1 | a0001c0001t0002g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3026-629A>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309272 | |||||||
| chr12:67309392 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3026-509G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309392 | |||||||
| chr12:67309406 | C | T | 67 | a0001c0001t0062g0145 a0001c0002t0001g0001 a0001c0002t0001g0007 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.3026-495C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309406 | |||||||
| chr12:67309464 | C | CAGTGGGT others(28): Show |
1 | a0001c0002t0050g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3026-436_3026-402d others(37): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 67309464 | ||||||
| chr12:67309511 | G | A | 3 | a0001c0001t0013g0018 a0001c0001t0032g0043 a0001c0001t0034g0042 |
4 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3026-390G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309511 | |||||||
| chr12:67309554 | G | A | 1 | a0001c0001t0003g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3026-347G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309554 | |||||||
| chr12:67309609 | T | C | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.3026-292T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309609 | |||||||
| chr12:67309797 | A | G | 3 | a0001c0001t0007g0092 a0001c0001t0007g0096 a0001c0001t0023g0097 |
3 | HG01261.hp1 HG01993.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3026-104A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309797 | |||||||
| chr12:67309843 | T | C | 1 | a0001c0001t0019g0160 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3026-58T>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309843 | |||||||
| chr12:67309877 | G | T | 1 | a0001c0001t0004g0173 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3026-24G>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 11/14 | chr12 | 67309877 | |||||||
| chr12:67310129 | C | A | 16 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.3196-23C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 12/14 | chr12 | 67310129 | |||||||
| chr12:67310369 | G | C | 1 | a0001c0001t0031g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3360+53G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67310369 | |||||||
| chr12:67310391 | A | G | 1 | a0001c0001t0023g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3360+75A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67310391 | |||||||
| chr12:67310491 | C | T | 4 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3360+175C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67310491 | |||||||
| chr12:67310685 | G | A | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3360+369G>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67310685 | |||||||
| chr12:67310755 | G | C | 4 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3360+439G>C | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67310755 | |||||||
| chr12:67310893 | C | T | 4 | a0001c0004t0014g0019 a0001c0004t0014g0074 a0001c0004t0014g0077 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3360+577C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67310893 | |||||||
| chr12:67311168 | C | A | 1 | a0001c0001t0046g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3361-525C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67311168 | |||||||
| chr12:67311230 | A | AGGTTTAT others(2): Show |
83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.3361-461_3361-453d others(11): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 67311230 | ||||||
| chr12:67311344 | A | G | 4 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(1): Show |
4 | HG02717.hp1 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-349A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67311344 | |||||||
| chr12:67311390 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0198 |
2 | HG00544.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.3361-303A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67311390 | |||||||
| chr12:67311407 | A | G | 147 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(144): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3361-286A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | chr12 | 67311407 | |||||||
| chr12:67311532 | T | TGTTTGAG others(124): Show |
1 | a0001c0002t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3361-151_3361-150i others(133): Show |
CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 67311532 | ||||||
| chr12:67311900 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3468+100C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 14/14 | chr12 | 67311900 | |||||||
| chr12:67311961 | C | A | 148 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0038 others(145): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3468+161C>A | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 14/14 | chr12 | 67311961 | |||||||
| chr12:67312000 | A | G | 1 | a0001c0001t0031g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3468+200A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 14/14 | chr12 | 67312000 | |||||||
| chr12:67312132 | T | G | 83 | a0001c0001t0020g0022 a0001c0001t0020g0037 a0001c0001t0020g0088 others(80): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.3468+332T>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 14/14 | chr12 | 67312132 | |||||||
| chr12:67312167 | AT | A | 106 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0001t0007g0064 others(103): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.3468+380delT | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 67312167 | ||||||
| chr12:67312229 | C | T | 1 | a0001c0001t0027g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3469-377C>T | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 14/14 | chr12 | 67312229 | |||||||
| chr12:67312559 | A | G | 1 | a0001c0002t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3469-47A>G | CAND1 | ENSG00000111530.13 | transcript | ENST00000545606.6 | protein_coding | 14/14 | chr12 | 67312559 |