Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79087 |
| ensemblid | ENSG00000182858.14 |
| hgncid | 19358 |
| symbol | ALG12 |
| name | ALG12 alpha-1,6-mannosyltransferase |
| refseq_nuc | NM_024105.4 |
| refseq_prot | NP_077010.1 |
| ensembl_nuc | ENST00000330817.11 |
| ensembl_prot | ENSP00000333813.5 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 49900229 |
| end | 49918438 |
| strand | - |
| ver | v1.2 |
| region | chr22:49900229-49918438 |
| region5000 | chr22:49895229-49923438 |
| regionname0 | ALG12_chr22_49900229_49918438 |
| regionname5000 | ALG12_chr22_49895229_49923438 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 488 | 299 | 80 | 55 | 119 | 12 | 31 | 81 | ALG12_chr22_49895229_49923438 | ALG12 | MAGKG others(483): Show |
chr22 | 49895229 | 49923438 |
| a0002 | 0/0 | 488 | 31 | 2 | 5 | 16 | 0 | 8 | 13 | ALG12_chr22_49895229_49923438 | ALG12 | MAGKG others(483): Show |
chr22 | 49895229 | 49923438 |
| a0003 | 0/0 | 488 | 12 | 0 | 0 | 7 | 0 | 5 | 6 | ALG12_chr22_49895229_49923438 | ALG12 | MAGKG others(483): Show |
chr22 | 49895229 | 49923438 |
| a0004 | 0/0 | 488 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | MAGKG others(483): Show |
chr22 | 49895229 | 49923438 |
| a0005 | 0/0 | 488 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | MAGKG others(483): Show |
chr22 | 49895229 | 49923438 |
| a0006 | 0/0 | 488 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | MAGKG others(483): Show |
chr22 | 49895229 | 49923438 |
| a0007 | 0/0 | 488 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | MAGKG others(483): Show |
chr22 | 49895229 | 49923438 |
| a0008 | 0/0 | 488 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | MAGKG others(483): Show |
chr22 | 49895229 | 49923438 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1464 | 196 | 19 | 46 | 103 | 7 | 19 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0001c0002 | 0/0 | 1464 | 78 | 43 | 6 | 15 | 4 | 10 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0001c0004 | 0/0 | 1464 | 11 | 8 | 1 | 0 | 0 | 2 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0001c0005 | 0/0 | 1464 | 8 | 7 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0001c0008 | 0/0 | 1464 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0001c0010 | 0/0 | 1464 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0001c0011 | 0/0 | 1464 | 1 | 0 | 0 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0001c0012 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0001c0015 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0002c0003 | 0/0 | 1464 | 30 | 1 | 5 | 16 | 0 | 8 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0002c0013 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0003c0006 | 0/0 | 1464 | 8 | 0 | 0 | 7 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0003c0007 | 0/0 | 1464 | 4 | 0 | 0 | 0 | 0 | 4 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0004c0009 | 0/0 | 1464 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0005c0016 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0006c0018 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0007c0014 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 | ||
| a0008c0017 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATGGC others(1459): Show |
chr22 | 49895229 | 49923438 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5330 | 124 | 3 | 41 | 62 | 5 | 11 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0002 | 0/0 | 5330 | 36 | 0 | 2 | 29 | 0 | 5 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0005 | 0/0 | 5330 | 13 | 13 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0012 | 0/0 | 5330 | 5 | 2 | 0 | 0 | 2 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0017 | 0/0 | 5326 | 3 | 0 | 0 | 3 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5321): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0041 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0043 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0044 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0045 | 0/0 | 5328 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5323): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0046 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0048 | 0/0 | 5274 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5269): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0049 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0050 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0052 | 0/0 | 5330 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0053 | 0/0 | 5330 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0054 | 0/0 | 5330 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0055 | 0/0 | 5328 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5323): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0056 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0057 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0001t0067 | 0/0 | 5330 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0003 | 0/0 | 5242 | 22 | 2 | 1 | 10 | 2 | 7 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5237): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0006 | 0/0 | 5385 | 5 | 5 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5380): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0007 | 0/0 | 5235 | 9 | 8 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5230): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0008 | 0/0 | 5242 | 9 | 8 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5237): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0010 | 0/0 | 5248 | 6 | 1 | 1 | 3 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5243): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0011 | 0/0 | 5249 | 5 | 5 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5244): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0015 | 0/0 | 5240 | 3 | 1 | 1 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5235): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0024 | 0/0 | 5385 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5380): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0025 | 0/0 | 5150 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5145): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0027 | 0/0 | 5251 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5246): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0029 | 0/0 | 5387 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5382): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0031 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5232): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0033 | 0/0 | 5242 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5237): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0034 | 0/0 | 5235 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5230): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0035 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5235): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0047 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0059 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5147): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0060 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5145): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0063 | 0/0 | 5248 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5243): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0064 | 0/0 | 5248 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5243): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0065 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5239): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0066 | 0/0 | 5249 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5244): Show |
chr22 | 49895229 | 49923438 |
| a0001c0002t0068 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5243): Show |
chr22 | 49895229 | 49923438 |
| a0001c0004t0009 | 0/0 | 5246 | 6 | 6 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5241): Show |
chr22 | 49895229 | 49923438 |
| a0001c0004t0018 | 0/0 | 5248 | 2 | 0 | 0 | 0 | 0 | 2 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5243): Show |
chr22 | 49895229 | 49923438 |
| a0001c0004t0021 | 0/0 | 5244 | 2 | 1 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5239): Show |
chr22 | 49895229 | 49923438 |
| a0001c0004t0030 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5243): Show |
chr22 | 49895229 | 49923438 |
| a0001c0005t0013 | 0/0 | 5246 | 3 | 3 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5241): Show |
chr22 | 49895229 | 49923438 |
| a0001c0005t0019 | 0/0 | 5244 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5239): Show |
chr22 | 49895229 | 49923438 |
| a0001c0005t0020 | 0/0 | 5242 | 2 | 1 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5237): Show |
chr22 | 49895229 | 49923438 |
| a0001c0005t0032 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5239): Show |
chr22 | 49895229 | 49923438 |
| a0001c0008t0023 | 0/0 | 5385 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5380): Show |
chr22 | 49895229 | 49923438 |
| a0001c0010t0061 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5245): Show |
chr22 | 49895229 | 49923438 |
| a0001c0011t0001 | 0/0 | 5330 | 1 | 0 | 0 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0012t0001 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0001c0015t0011 | 0/0 | 5249 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5244): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0004 | 0/0 | 5244 | 16 | 0 | 2 | 9 | 0 | 5 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5239): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0014 | 0/0 | 5242 | 4 | 0 | 0 | 4 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5237): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0016 | 0/0 | 5242 | 3 | 0 | 1 | 0 | 0 | 2 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5237): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0026 | 0/0 | 5218 | 2 | 0 | 0 | 1 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5213): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0036 | 0/0 | 5244 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5239): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0037 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5239): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0038 | 0/0 | 5242 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5237): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0040 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5245): Show |
chr22 | 49895229 | 49923438 |
| a0002c0003t0058 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5388): Show |
chr22 | 49895229 | 49923438 |
| a0002c0013t0028 | 0/0 | 5212 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5207): Show |
chr22 | 49895229 | 49923438 |
| a0003c0006t0006 | 0/0 | 5385 | 8 | 0 | 0 | 7 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5380): Show |
chr22 | 49895229 | 49923438 |
| a0003c0007t0001 | 0/0 | 5330 | 2 | 0 | 0 | 0 | 0 | 2 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0003c0007t0042 | 0/0 | 5328 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5323): Show |
chr22 | 49895229 | 49923438 |
| a0003c0007t0051 | 0/0 | 5330 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5325): Show |
chr22 | 49895229 | 49923438 |
| a0004c0009t0022 | 0/0 | 5385 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5380): Show |
chr22 | 49895229 | 49923438 |
| a0005c0016t0039 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5245): Show |
chr22 | 49895229 | 49923438 |
| a0006c0018t0062 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5245): Show |
chr22 | 49895229 | 49923438 |
| a0007c0014t0013 | 0/0 | 5246 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5241): Show |
chr22 | 49895229 | 49923438 |
| a0008c0017t0007 | 0/0 | 5235 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | ATCTT others(5230): Show |
chr22 | 49895229 | 49923438 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/1 | 49 | 2 | 21 | 16 | 2 | 6 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 8 | 1 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0003 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0005g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0005g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0005g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0012g0014 | 0/0 | 4 | 2 | 0 | 0 | 2 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0017g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0017g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0041g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0043g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0044g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0045g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0046g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0048g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0049g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0050g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0052g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0053g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0054g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0055g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0056g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0057g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0001t0067g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0006g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0007g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0008g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0010g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0010g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0010g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0011g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0015g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0015g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0024g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0025g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0027g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0029g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0031g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0033g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0034g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0035g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0047g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0059g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0060g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0063g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0064g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0065g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0066g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0002t0068g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0004t0009g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0004t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0004t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0004t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0004t0018g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0004t0021g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0004t0030g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0005t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0005t0013g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0005t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0005t0019g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0005t0020g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0005t0032g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0008t0023g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0008t0023g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0010t0061g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0011t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0012t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0001c0015t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0004g0007 | 0/0 | 6 | 0 | 1 | 2 | 0 | 3 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0004g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0014g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0014g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0014g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0016g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0026g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0026g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0036g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0037g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0038g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0040g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0003t0058g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0002c0013t0028g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0006t0006g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0006t0006g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0006t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0006t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0006t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0006t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0007t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0007t0042g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0003c0007t0051g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0004c0009t0022g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0004c0009t0022g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0005c0016t0039g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0006c0018t0062g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0007c0014t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| a0008c0017t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0015 | g0023 | EUR | GBR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00099 | hp2 | a0001 | c0001 | t0012 | g0014 | EUR | GBR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00140 | hp1 | a0001 | c0002 | t0035 | g0081 | EUR | GBR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00280 | hp2 | a0001 | c0011 | t0001 | g0139 | EUR | FIN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00323 | hp1 | a0001 | c0001 | t0012 | g0014 | EUR | FIN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0026 | EUR | FIN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00438 | hp2 | a0002 | c0003 | t0004 | g0059 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00597 | hp2 | a0002 | c0003 | t0038 | g0051 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00642 | hp1 | a0002 | c0003 | t0016 | g0015 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00741 | hp1 | a0002 | c0003 | t0058 | g0177 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01074 | hp2 | a0001 | c0002 | t0015 | g0082 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0026 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01109 | hp1 | a0001 | c0001 | t0052 | g0144 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01109 | hp2 | a0001 | c0010 | t0061 | g0178 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01243 | hp1 | a0001 | c0002 | t0007 | g0008 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01243 | hp2 | a0001 | c0002 | t0008 | g0009 | AMR | PUR | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01255 | hp2 | a0001 | c0005 | t0020 | g0025 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01256 | hp1 | a0001 | c0002 | t0063 | g0182 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01361 | hp2 | a0001 | c0004 | t0021 | g0027 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01433 | hp1 | a0002 | c0003 | t0004 | g0007 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0091 | EUR | IBS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01884 | hp1 | a0001 | c0002 | t0011 | g0185 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01884 | hp2 | a0001 | c0004 | t0021 | g0027 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01891 | hp1 | a0001 | c0002 | t0031 | g0074 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01891 | hp2 | a0001 | c0004 | t0009 | g0016 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01934 | hp1 | a0001 | c0001 | t0053 | g0172 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01934 | hp2 | a0001 | c0001 | t0054 | g0145 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01975 | hp2 | a0002 | c0003 | t0004 | g0061 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02040 | hp1 | a0001 | c0002 | t0010 | g0047 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02040 | hp2 | a0003 | c0006 | t0006 | g0032 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02055 | hp1 | a0001 | c0002 | t0008 | g0077 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02055 | hp2 | a0001 | c0002 | t0025 | g0030 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02056 | hp1 | a0002 | c0003 | t0004 | g0007 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02071 | hp2 | a0001 | c0001 | t0046 | g0141 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02145 | hp2 | a0001 | c0002 | t0029 | g0070 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02257 | hp2 | a0001 | c0002 | t0006 | g0033 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02280 | hp2 | a0001 | c0002 | t0027 | g0049 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02300 | hp2 | a0001 | c0002 | t0010 | g0184 | AMR | PEL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02451 | hp1 | a0001 | c0004 | t0030 | g0096 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02451 | hp2 | a0004 | c0009 | t0022 | g0108 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02572 | hp2 | a0002 | c0013 | t0028 | g0052 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0021 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02615 | hp1 | a0001 | c0004 | t0009 | g0016 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02615 | hp2 | a0001 | c0002 | t0007 | g0076 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02622 | hp1 | a0001 | c0002 | t0010 | g0183 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02622 | hp2 | a0001 | c0002 | t0008 | g0073 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02698 | hp1 | a0002 | c0003 | t0004 | g0007 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02698 | hp2 | a0001 | c0002 | t0033 | g0069 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0034 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02717 | hp2 | a0001 | c0002 | t0006 | g0033 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02723 | hp2 | a0001 | c0004 | t0009 | g0093 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0072 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02809 | hp1 | a0001 | c0002 | t0008 | g0009 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02809 | hp2 | a0001 | c0002 | t0008 | g0009 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02886 | hp1 | a0001 | c0002 | t0027 | g0049 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02886 | hp2 | a0001 | c0005 | t0019 | g0024 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02895 | hp1 | a0001 | c0002 | t0007 | g0008 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02895 | hp2 | a0001 | c0002 | t0008 | g0009 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02896 | hp1 | a0001 | c0002 | t0006 | g0034 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0111 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02897 | hp2 | a0001 | c0002 | t0007 | g0083 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02922 | hp1 | a0005 | c0016 | t0039 | g0098 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02922 | hp2 | a0001 | c0002 | t0011 | g0050 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02965 | hp1 | a0001 | c0015 | t0011 | g0187 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02965 | hp2 | a0001 | c0002 | t0007 | g0078 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02970 | hp1 | a0001 | c0002 | t0008 | g0009 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02976 | hp1 | a0001 | c0002 | t0068 | g0188 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02976 | hp2 | a0001 | c0002 | t0059 | g0102 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03017 | hp2 | a0003 | c0006 | t0006 | g0110 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03041 | hp1 | a0001 | c0002 | t0060 | g0103 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03098 | hp2 | a0001 | c0002 | t0008 | g0065 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03130 | hp1 | a0004 | c0009 | t0022 | g0109 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0041 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03139 | hp1 | a0006 | c0018 | t0062 | g0179 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03139 | hp2 | a0001 | c0008 | t0023 | g0100 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03195 | hp1 | a0001 | c0002 | t0011 | g0050 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03209 | hp1 | a0001 | c0002 | t0025 | g0030 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03209 | hp2 | a0007 | c0014 | t0013 | g0089 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0022 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03225 | hp2 | a0001 | c0008 | t0023 | g0101 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03239 | hp1 | a0002 | c0003 | t0004 | g0056 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03239 | hp2 | a0001 | c0002 | t0003 | g0080 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0084 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0063 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0021 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03540 | hp2 | a0001 | c0005 | t0013 | g0087 | AFR | GWD | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03579 | hp1 | a0001 | c0002 | t0007 | g0008 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03654 | hp1 | a0002 | c0003 | t0016 | g0015 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0066 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03688 | hp1 | a0003 | c0007 | t0051 | g0116 | SAS | STU | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03688 | hp2 | a0002 | c0003 | t0026 | g0117 | SAS | STU | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03704 | hp1 | a0002 | c0003 | t0004 | g0007 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03704 | hp2 | a0001 | c0002 | t0064 | g0181 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03710 | hp1 | a0001 | c0004 | t0018 | g0028 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0071 | SAS | PJL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | BEB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0151 | SAS | BEB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03927 | hp1 | a0003 | c0007 | t0042 | g0115 | SAS | BEB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03927 | hp2 | a0002 | c0003 | t0004 | g0062 | SAS | BEB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03942 | hp1 | a0001 | c0001 | t0067 | g0167 | SAS | BEB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03942 | hp2 | a0001 | c0004 | t0018 | g0028 | SAS | BEB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG04115 | hp1 | a0003 | c0007 | t0001 | g0036 | SAS | STU | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG04204 | hp1 | a0002 | c0003 | t0004 | g0007 | SAS | STU | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG04204 | hp2 | a0003 | c0007 | t0001 | g0036 | SAS | STU | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG04228 | hp1 | a0002 | c0003 | t0016 | g0015 | SAS | STU | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG04228 | hp2 | a0001 | c0002 | t0010 | g0048 | SAS | STU | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18522 | hp1 | a0001 | c0002 | t0024 | g0035 | AFR | YRI | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18522 | hp2 | a0001 | c0002 | t0007 | g0008 | AFR | YRI | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0090 | EAS | CHB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18747 | hp1 | a0001 | c0001 | t0045 | g0112 | EAS | CHB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18747 | hp2 | a0001 | c0001 | t0017 | g0040 | EAS | CHB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18906 | hp1 | a0001 | c0002 | t0034 | g0075 | AFR | YRI | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0041 | AFR | YRI | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18939 | hp2 | a0002 | c0003 | t0014 | g0060 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18940 | hp1 | a0003 | c0006 | t0006 | g0106 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18943 | hp1 | a0003 | c0006 | t0006 | g0105 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18947 | hp1 | a0002 | c0003 | t0014 | g0020 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18950 | hp1 | a0003 | c0006 | t0006 | g0107 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18952 | hp2 | a0002 | c0003 | t0004 | g0007 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18954 | hp2 | a0001 | c0001 | t0017 | g0149 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18960 | hp1 | a0001 | c0002 | t0047 | g0174 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18965 | hp2 | a0001 | c0002 | t0065 | g0099 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18966 | hp2 | a0003 | c0006 | t0006 | g0032 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0067 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18967 | hp2 | a0002 | c0003 | t0004 | g0054 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18968 | hp1 | a0001 | c0001 | t0044 | g0176 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18969 | hp1 | a0001 | c0001 | t0056 | g0122 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18974 | hp2 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18979 | hp2 | a0001 | c0001 | t0049 | g0143 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18980 | hp1 | a0001 | c0001 | t0043 | g0158 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18980 | hp2 | a0002 | c0003 | t0014 | g0020 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18982 | hp2 | a0003 | c0006 | t0006 | g0031 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18989 | hp2 | a0002 | c0003 | t0004 | g0058 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18993 | hp1 | a0001 | c0001 | t0041 | g0157 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA18994 | hp2 | a0002 | c0003 | t0014 | g0053 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19001 | hp1 | a0002 | c0003 | t0026 | g0166 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19001 | hp2 | a0001 | c0001 | t0057 | g0159 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19004 | hp1 | a0003 | c0006 | t0006 | g0031 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19007 | hp2 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19009 | hp1 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19009 | hp2 | a0001 | c0012 | t0001 | g0130 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19012 | hp1 | a0002 | c0003 | t0037 | g0055 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19030 | hp1 | a0001 | c0005 | t0013 | g0085 | AFR | LWK | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19030 | hp2 | a0002 | c0003 | t0040 | g0097 | AFR | LWK | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19043 | hp1 | a0001 | c0002 | t0011 | g0186 | AFR | LWK | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19043 | hp2 | a0001 | c0004 | t0009 | g0016 | AFR | LWK | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19065 | hp1 | a0002 | c0003 | t0004 | g0013 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19066 | hp1 | a0001 | c0001 | t0050 | g0171 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19066 | hp2 | a0001 | c0001 | t0017 | g0040 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19067 | hp1 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19081 | hp1 | a0001 | c0002 | t0010 | g0048 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19088 | hp1 | a0001 | c0002 | t0010 | g0047 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0022 | AFR | YRI | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA19240 | hp2 | a0001 | c0002 | t0011 | g0180 | AFR | YRI | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA20129 | hp1 | a0001 | c0005 | t0019 | g0024 | AFR | ASW | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0008 | AFR | ASW | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA20905 | hp2 | a0001 | c0001 | t0048 | g0142 | SAS | GIH | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG01123 | hp2 | a0002 | c0003 | t0036 | g0057 | AMR | CLM | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02109 | hp2 | a0001 | c0002 | t0007 | g0008 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02486 | hp1 | a0001 | c0004 | t0009 | g0094 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02486 | hp2 | a0001 | c0002 | t0066 | g0104 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02559 | hp1 | a0001 | c0002 | t0024 | g0035 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03471 | hp1 | a0001 | c0005 | t0013 | g0086 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG03471 | hp2 | a0001 | c0005 | t0020 | g0025 | AFR | MSL | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG06807 | hp1 | a0001 | c0004 | t0009 | g0095 | AFR | USA | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| HG06807 | hp2 | a0008 | c0017 | t0007 | g0079 | AFR | USA | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA20300 | hp2 | a0001 | c0005 | t0032 | g0088 | AFR | USA | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA21309 | hp1 | a0001 | c0002 | t0015 | g0023 | AFR | LWK | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| NA21309 | hp2 | a0001 | c0001 | t0055 | g0152 | AFR | LWK | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | ALG12_chr22_49895229_49923438 | ALG12 | chr22 | 49895229 | 49923438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49903880 | C | G | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1425G>C | p.Gln475His | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1679/5330 | 1425/1467 | 475/488 | chr22 | 49903880 | |||
| chr22:49904240 | T | C | 2 | a0002 a0005 |
32 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
missense_variant | MODERATE | c.1177A>G | p.Ile393Val | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 9/10 | 1431/5330 | 1177/1467 | 393/488 | chr22 | 49904240 | |||
| chr22:49909314 | C | T | 1 | a0004 | 2 | HG02451.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.698G>A | p.Arg233Gln | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/10 | 952/5330 | 698/1467 | 233/488 | chr22 | 49909314 | |||
| chr22:49909906 | T | C | 1 | a0005 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.652A>G | p.Ile218Val | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/10 | 906/5330 | 652/1467 | 218/488 | chr22 | 49909906 | |||
| chr22:49909927 | G | A | 1 | a0003 | 12 | HG02040.hp2 HG03017.hp2 HG03688.hp1 others(9): Show |
missense_variant | MODERATE | c.631C>T | p.Arg211Cys | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/10 | 885/5330 | 631/1467 | 211/488 | chr22 | 49909927 | |||
| chr22:49913438 | G | A | 1 | a0008 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.242C>T | p.Ala81Val | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/10 | 496/5330 | 242/1467 | 81/488 | chr22 | 49913438 | |||
| chr22:49913738 | G | A | 1 | a0006 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.28C>T | p.Arg10Trp | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 2/10 | 282/5330 | 28/1467 | 10/488 | chr22 | 49913738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49903943 | G | A | 1 | a0001c0012 | 1 | NA19009.hp2 | synonymous_variant | LOW | c.1362C>T | p.Val454Val | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1616/5330 | 1362/1467 | 454/488 | chr22 | 49903943 | |||
| chr22:49904006 | G | A | 1 | a0002c0013 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1299C>T | p.Leu433Leu | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1553/5330 | 1299/1467 | 433/488 | chr22 | 49904006 | |||
| chr22:49904470 | C | T | 1 | a0001c0011 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.1029G>A | p.Ala343Ala | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 8/10 | 1283/5330 | 1029/1467 | 343/488 | chr22 | 49904470 | |||
| chr22:49907774 | G | A | 2 | a0001c0005 a0007c0014 |
9 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(6): Show |
synonymous_variant | LOW | c.939C>T | p.Ile313Ile | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/10 | 1193/5330 | 939/1467 | 313/488 | chr22 | 49907774 | |||
| chr22:49907828 | T | C | 14 | a0001c0002 a0001c0004 a0001c0005 others(11): Show |
146 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(143): Show |
synonymous_variant | LOW | c.885A>G | p.Ala295Ala | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/10 | 1139/5330 | 885/1467 | 295/488 | chr22 | 49907828 | |||
| chr22:49907903 | G | A | 1 | a0001c0015 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.810C>T | p.Arg270Arg | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/10 | 1064/5330 | 810/1467 | 270/488 | chr22 | 49907903 | |||
| chr22:49909913 | C | T | 1 | a0001c0008 | 2 | HG03139.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.645G>A | p.Pro215Pro | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/10 | 899/5330 | 645/1467 | 215/488 | chr22 | 49909913 | |||
| chr22:49913667 | C | T | 1 | a0001c0004 | 11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
synonymous_variant | LOW | c.99G>A | p.Val33Val | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 2/10 | 353/5330 | 99/1467 | 33/488 | chr22 | 49913667 | |||
| chr22:49913718 | C | G | 1 | a0001c0010 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.48G>C | p.Leu16Leu | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 2/10 | 302/5330 | 48/1467 | 16/488 | chr22 | 49913718 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49900273 | T | TA | 4 | a0001c0002t0011 a0001c0002t0027 a0001c0002t0066 others(1): Show |
9 | HG01884.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3564dupT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 3564 | chr22 | 49900273 | ||||||
| chr22:49900307 | G | T | 1 | a0002c0013t0028 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3531C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 3531 | chr22 | 49900307 | ||||||
| chr22:49900528 | A | C | 11 | a0001c0002t0010 a0001c0002t0011 a0001c0002t0027 others(8): Show |
22 | HG01256.hp1 HG01884.hp1 HG02040.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3310T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 3310 | chr22 | 49900528 | ||||||
| chr22:49900689 | G | A | 1 | a0001c0008t0023 | 2 | HG03139.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3149C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 3149 | chr22 | 49900689 | ||||||
| chr22:49900730 | G | A | 39 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(36): Show |
114 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3108C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 3108 | chr22 | 49900730 | ||||||
| chr22:49900790 | C | T | 1 | a0001c0002t0035 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3048G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 3048 | chr22 | 49900790 | ||||||
| chr22:49900821 | A | G | 49 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(46): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*3017T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 3017 | chr22 | 49900821 | ||||||
| chr22:49900822 | A | T | 49 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(46): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*3016T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 3016 | chr22 | 49900822 | ||||||
| chr22:49900854 | G | C | 5 | a0001c0005t0013 a0001c0005t0019 a0001c0005t0020 others(2): Show |
9 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2984C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2984 | chr22 | 49900854 | ||||||
| chr22:49900887 | G | A | 1 | a0001c0001t0049 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2951C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2951 | chr22 | 49900887 | ||||||
| chr22:49901134 | T | C | 1 | a0001c0001t0050 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2704A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2704 | chr22 | 49901134 | ||||||
| chr22:49901186 | C | G | 1 | a0002c0003t0036 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2652G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2652 | chr22 | 49901186 | ||||||
| chr22:49901271 | C | A | 1 | a0001c0004t0030 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2567G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2567 | chr22 | 49901271 | ||||||
| chr22:49901329 | T | C | 7 | a0001c0001t0002 a0001c0001t0044 a0001c0001t0045 others(4): Show |
42 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2509A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2509 | chr22 | 49901329 | ||||||
| chr22:49901334 | G | A | 1 | a0002c0003t0037 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2504C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2504 | chr22 | 49901334 | ||||||
| chr22:49901340 | C | T | 49 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(46): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2498G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2498 | chr22 | 49901340 | ||||||
| chr22:49901457 | ATG | A | 11 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(8): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2379_*2380delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2379 | chr22 | 49901457 | ||||||
| chr22:49901486 | C | T | 1 | a0001c0010t0061 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2352G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2352 | chr22 | 49901486 | ||||||
| chr22:49901503 | TGATTGCA others(49): Show |
T | 1 | a0001c0001t0048 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2279_*2334delGTGC others(52): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2279 | chr22 | 49901503 | ||||||
| chr22:49901531 | G | A | 1 | a0001c0002t0011 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2307C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2307 | chr22 | 49901531 | ||||||
| chr22:49901560 | G | A | 1 | a0003c0007t0051 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2278C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2278 | chr22 | 49901560 | ||||||
| chr22:49901562 | T | C | 1 | a0002c0003t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2276A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2276 | chr22 | 49901562 | ||||||
| chr22:49901604 | TTGTG | T | 1 | a0001c0001t0017 | 3 | NA18747.hp2 NA18954.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2230_*2233delCACA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2230 | chr22 | 49901604 | ||||||
| chr22:49901642 | GCA | G | 38 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(35): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2194_*2195delTG | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2194 | chr22 | 49901642 | ||||||
| chr22:49901652 | T | TTCTG | 49 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(46): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2185_*2186insCAGA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2185 | chr22 | 49901652 | ||||||
| chr22:49901682 | G | A | 1 | a0001c0002t0008 | 9 | HG01243.hp2 HG02055.hp1 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2156C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2156 | chr22 | 49901682 | ||||||
| chr22:49901718 | G | T | 6 | a0002c0003t0004 a0002c0003t0014 a0002c0003t0016 others(3): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2120C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2120 | chr22 | 49901718 | ||||||
| chr22:49901749 | T | C | 1 | a0001c0002t0063 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2089A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2089 | chr22 | 49901749 | ||||||
| chr22:49901758 | T | TATGCATG others(58): Show |
46 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(43): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2079_*2080insCCAC others(61): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2079 | chr22 | 49901758 | ||||||
| chr22:49901767 | TA | T | 3 | a0001c0002t0025 a0001c0002t0059 a0001c0002t0060 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2070delT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2070 | chr22 | 49901767 | ||||||
| chr22:49901769 | A | G | 3 | a0001c0002t0025 a0001c0002t0059 a0001c0002t0060 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2069T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2069 | chr22 | 49901769 | ||||||
| chr22:49901784 | CTG | C | 6 | a0002c0003t0004 a0002c0003t0014 a0002c0003t0016 others(3): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2052_*2053delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2052 | chr22 | 49901784 | ||||||
| chr22:49901784 | CTGTG | C | 3 | a0001c0002t0025 a0001c0002t0059 a0001c0002t0060 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2050_*2053delCACA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2050 | chr22 | 49901784 | ||||||
| chr22:49901795 | A | G | 3 | a0001c0002t0025 a0001c0002t0059 a0001c0002t0060 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2043T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2043 | chr22 | 49901795 | ||||||
| chr22:49901808 | G | GTGTGCAT others(24): Show |
3 | a0001c0002t0025 a0001c0002t0059 a0001c0002t0060 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2029_*2030insTTAC others(27): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2029 | chr22 | 49901808 | ||||||
| chr22:49901816 | G | A | 2 | a0002c0003t0040 a0005c0016t0039 |
2 | HG02922.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2022C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2022 | chr22 | 49901816 | ||||||
| chr22:49901823 | CTG | C | 5 | a0001c0002t0010 a0001c0002t0063 a0001c0002t0064 others(2): Show |
12 | HG01255.hp2 HG01256.hp1 HG02040.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2013_*2014delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2013 | chr22 | 49901823 | ||||||
| chr22:49901827 | G | GTGTGGTA | 3 | a0001c0002t0025 a0001c0002t0059 a0001c0002t0060 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2010_*2011insTACC others(3): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 2010 | chr22 | 49901827 | ||||||
| chr22:49901855 | CTG | C | 49 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(46): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1981_*1982delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1981 | chr22 | 49901855 | ||||||
| chr22:49901894 | CTG | C | 12 | a0002c0003t0004 a0002c0003t0014 a0002c0003t0016 others(9): Show |
33 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1942_*1943delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1942 | chr22 | 49901894 | ||||||
| chr22:49901907 | T | C | 1 | a0001c0001t0052 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1931A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1931 | chr22 | 49901907 | ||||||
| chr22:49901919 | C | T | 1 | a0001c0002t0047 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1919G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1919 | chr22 | 49901919 | ||||||
| chr22:49901927 | CTG | C | 3 | a0001c0001t0055 a0001c0005t0032 a0002c0003t0026 |
4 | HG03688.hp2 NA19001.hp1 NA20300.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1909_*1910delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1909 | chr22 | 49901927 | ||||||
| chr22:49901940 | C | T | 49 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(46): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1898G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1898 | chr22 | 49901940 | ||||||
| chr22:49901941 | G | A | 10 | a0001c0002t0010 a0001c0002t0011 a0001c0002t0027 others(7): Show |
20 | HG01109.hp2 HG01256.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1897C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1897 | chr22 | 49901941 | ||||||
| chr22:49901945 | A | T | 1 | a0001c0002t0033 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1893T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1893 | chr22 | 49901945 | ||||||
| chr22:49901998 | ACT | A | 11 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(8): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1838_*1839delAG | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1838 | chr22 | 49901998 | ||||||
| chr22:49902005 | A | G | 1 | a0001c0002t0060 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1833T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1833 | chr22 | 49902005 | ||||||
| chr22:49902017 | G | A | 1 | a0001c0002t0034 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1821C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1821 | chr22 | 49902017 | ||||||
| chr22:49902024 | C | T | 1 | a0001c0001t0046 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1814G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1814 | chr22 | 49902024 | ||||||
| chr22:49902063 | CTG | C | 38 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(35): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1773_*1774delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1773 | chr22 | 49902063 | ||||||
| chr22:49902077 | C | T | 4 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0034 others(1): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1761G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1761 | chr22 | 49902077 | ||||||
| chr22:49902085 | G | C | 7 | a0001c0002t0003 a0001c0002t0008 a0001c0002t0015 others(4): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1753C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1753 | chr22 | 49902085 | ||||||
| chr22:49902092 | C | G | 3 | a0001c0002t0011 a0001c0002t0066 a0001c0015t0011 |
7 | HG01884.hp1 HG02486.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1746G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1746 | chr22 | 49902092 | ||||||
| chr22:49902095 | G | A | 1 | a0001c0002t0068 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1743 | chr22 | 49902095 | ||||||
| chr22:49902102 | CTG | C | 4 | a0001c0001t0045 a0002c0003t0040 a0002c0003t0058 others(1): Show |
4 | HG00741.hp1 HG02922.hp1 NA18747.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1734_*1735delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1734 | chr22 | 49902102 | ||||||
| chr22:49902114 | G | A | 4 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0034 others(1): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1724C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1724 | chr22 | 49902114 | ||||||
| chr22:49902116 | TA | T | 4 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0034 others(1): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1721delT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1721 | chr22 | 49902116 | ||||||
| chr22:49902118 | A | G | 4 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0034 others(1): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1720T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1720 | chr22 | 49902118 | ||||||
| chr22:49902133 | CTG | C | 3 | a0001c0004t0009 a0001c0004t0021 a0002c0003t0038 |
9 | HG00597.hp2 HG01361.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1703_*1704delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1703 | chr22 | 49902133 | ||||||
| chr22:49902134 | T | C | 1 | a0001c0002t0064 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1704A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1704 | chr22 | 49902134 | ||||||
| chr22:49902142 | GTGTGT | G | 4 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0034 others(1): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1691_*1695delACAC others(1): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1691 | chr22 | 49902142 | ||||||
| chr22:49902143 | T | A | 10 | a0001c0002t0010 a0001c0002t0011 a0001c0002t0027 others(7): Show |
20 | HG01109.hp2 HG01256.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1695A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1695 | chr22 | 49902143 | ||||||
| chr22:49902156 | T | TA | 4 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0034 others(1): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1681_*1682insT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1681 | chr22 | 49902156 | ||||||
| chr22:49902157 | G | A | 4 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0034 others(1): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1681C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1681 | chr22 | 49902157 | ||||||
| chr22:49902165 | G | A | 1 | a0001c0001t0053 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1673C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1673 | chr22 | 49902165 | ||||||
| chr22:49902172 | CTG | C | 1 | a0002c0003t0016 | 3 | HG00642.hp1 HG03654.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1664_*1665delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1664 | chr22 | 49902172 | ||||||
| chr22:49902182 | T | A | 1 | a0001c0002t0064 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1656A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1656 | chr22 | 49902182 | ||||||
| chr22:49902204 | A | G | 4 | a0001c0002t0007 a0001c0002t0031 a0001c0002t0034 others(1): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1634T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1634 | chr22 | 49902204 | ||||||
| chr22:49902209 | C | T | 1 | a0001c0001t0045 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1629G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1629 | chr22 | 49902209 | ||||||
| chr22:49902213 | GTGTGGTG others(28): Show |
G | 3 | a0001c0002t0007 a0001c0002t0034 a0008c0017t0007 |
11 | HG01243.hp1 HG02109.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1590_*1624delGTGC others(31): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1590 | chr22 | 49902213 | ||||||
| chr22:49902240 | C | T | 3 | a0001c0002t0031 a0002c0003t0026 a0002c0013t0028 |
4 | HG01891.hp1 HG02572.hp2 HG03688.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1598G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1598 | chr22 | 49902240 | ||||||
| chr22:49902248 | C | CTG | 35 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0008 others(32): Show |
100 | HG00323.hp2 HG00423.hp2 HG00741.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1588_*1589dupCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1589 | chr22 | 49902248 | ||||||
| chr22:49902250 | GTGTATGC others(21): Show |
G | 2 | a0002c0003t0026 a0002c0013t0028 |
3 | HG02572.hp2 HG03688.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1560_*1587delGTGC others(24): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1560 | chr22 | 49902250 | ||||||
| chr22:49902262 | T | A | 1 | a0001c0002t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1576A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1576 | chr22 | 49902262 | ||||||
| chr22:49902268 | C | T | 1 | a0001c0001t0001 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1570G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1570 | chr22 | 49902268 | ||||||
| chr22:49902270 | T | C | 1 | a0001c0002t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1568 | chr22 | 49902270 | ||||||
| chr22:49902278 | C | CTG | 46 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(43): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1558_*1559dupCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1559 | chr22 | 49902278 | ||||||
| chr22:49902286 | A | C | 1 | a0002c0003t0026 | 2 | HG03688.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1552T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1552 | chr22 | 49902286 | ||||||
| chr22:49902289 | G | A | 1 | a0001c0002t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1549 | chr22 | 49902289 | ||||||
| chr22:49902313 | G | T | 1 | a0001c0002t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1525C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1525 | chr22 | 49902313 | ||||||
| chr22:49902324 | A | G | 1 | a0001c0002t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1514T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1514 | chr22 | 49902324 | ||||||
| chr22:49902331 | C | T | 1 | a0001c0001t0044 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1507G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1507 | chr22 | 49902331 | ||||||
| chr22:49902339 | CTG | C | 48 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(45): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1497_*1498delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1497 | chr22 | 49902339 | ||||||
| chr22:49902340 | T | G | 1 | a0001c0002t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1498A>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1498 | chr22 | 49902340 | ||||||
| chr22:49902394 | T | C | 1 | a0001c0001t0054 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1444A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1444 | chr22 | 49902394 | ||||||
| chr22:49902409 | C | CGTGTGCA others(13): Show |
1 | a0002c0003t0016 | 3 | HG00642.hp1 HG03654.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1428_*1429insACCA others(16): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1428 | chr22 | 49902409 | ||||||
| chr22:49902409 | C | CGTGTGCA others(15): Show |
36 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(33): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1428_*1429insACCA others(18): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1428 | chr22 | 49902409 | ||||||
| chr22:49902410 | A | G | 49 | a0001c0001t0001 a0001c0002t0003 a0001c0002t0006 others(46): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1428T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1428 | chr22 | 49902410 | ||||||
| chr22:49902431 | TGTGTGCA others(1): Show |
T | 9 | a0001c0002t0006 a0001c0002t0024 a0001c0002t0025 others(6): Show |
24 | HG02040.hp2 HG02055.hp2 HG02257.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1399_*1406delGTGC others(4): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1399 | chr22 | 49902431 | ||||||
| chr22:49902439 | C | CTGTGTAT others(7): Show |
1 | a0001c0002t0027 | 2 | HG02280.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1398_*1399insACCA others(10): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1398 | chr22 | 49902439 | ||||||
| chr22:49902439 | CGTGTGCA others(141): Show |
C | 1 | a0001c0002t0029 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1251_*1398del | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1251 | chr22 | 49902439 | ||||||
| chr22:49902469 | C | T | 1 | a0001c0001t0043 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1369 | chr22 | 49902469 | ||||||
| chr22:49902470 | G | A | 6 | a0002c0003t0004 a0002c0003t0014 a0002c0003t0016 others(3): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1368C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1368 | chr22 | 49902470 | ||||||
| chr22:49902477 | CTG | C | 3 | a0001c0002t0011 a0001c0002t0066 a0001c0015t0011 |
7 | HG01884.hp1 HG02486.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1359_*1360delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1359 | chr22 | 49902477 | ||||||
| chr22:49902477 | CTGTGTGG | C | 6 | a0001c0002t0006 a0001c0002t0024 a0001c0008t0023 others(3): Show |
20 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1360delCCAC others(3): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1354 | chr22 | 49902477 | ||||||
| chr22:49902507 | A | G | 6 | a0001c0002t0006 a0001c0002t0024 a0001c0008t0023 others(3): Show |
20 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1331T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1331 | chr22 | 49902507 | ||||||
| chr22:49902514 | C | CTGTGTGG | 6 | a0001c0002t0006 a0001c0002t0024 a0001c0008t0023 others(3): Show |
20 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1323_*1324insCCAC others(3): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1323 | chr22 | 49902514 | ||||||
| chr22:49902516 | GTGTATGC others(22): Show |
G | 3 | a0001c0002t0025 a0001c0002t0059 a0001c0002t0060 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1293_*1321delGTGC others(25): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1293 | chr22 | 49902516 | ||||||
| chr22:49902528 | TA | T | 6 | a0001c0002t0006 a0001c0002t0024 a0001c0008t0023 others(3): Show |
20 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1309delT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1309 | chr22 | 49902528 | ||||||
| chr22:49902530 | A | G | 6 | a0001c0002t0006 a0001c0002t0024 a0001c0008t0023 others(3): Show |
20 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1308T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1308 | chr22 | 49902530 | ||||||
| chr22:49902537 | C | T | 6 | a0002c0003t0004 a0002c0003t0014 a0002c0003t0016 others(3): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1301G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1301 | chr22 | 49902537 | ||||||
| chr22:49902538 | G | A | 6 | a0001c0002t0006 a0001c0002t0024 a0001c0008t0023 others(3): Show |
20 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1300C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1300 | chr22 | 49902538 | ||||||
| chr22:49902539 | C | T | 7 | a0001c0001t0001 a0001c0002t0006 a0001c0002t0024 others(4): Show |
21 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1299G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1299 | chr22 | 49902539 | ||||||
| chr22:49902545 | C | CTG | 42 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(39): Show |
137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1291_*1292dupCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1292 | chr22 | 49902545 | ||||||
| chr22:49902545 | CTGTG | C | 1 | a0001c0001t0001 | 4 | HG03834.hp1 NA18953.hp1 NA18965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1289_*1292delCACA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1289 | chr22 | 49902545 | ||||||
| chr22:49902572 | T | C | 1 | a0002c0013t0028 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1266A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1266 | chr22 | 49902572 | ||||||
| chr22:49902578 | CTG | C | 15 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(12): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1258_*1259delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1258 | chr22 | 49902578 | ||||||
| chr22:49902617 | CTG | C | 2 | a0001c0005t0019 a0001c0005t0020 |
4 | HG01255.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1219_*1220delCA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1219 | chr22 | 49902617 | ||||||
| chr22:49902633 | A | G | 1 | a0001c0002t0029 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1205 | chr22 | 49902633 | ||||||
| chr22:49902633 | A | T | 6 | a0002c0003t0004 a0002c0003t0014 a0002c0003t0016 others(3): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1205T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1205 | chr22 | 49902633 | ||||||
| chr22:49902648 | CTGTGTGG others(136): Show |
C | 41 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(38): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1047_*1189del | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1047 | chr22 | 49902648 | ||||||
| chr22:49902648 | CTGTGTGG others(138): Show |
C | 1 | a0001c0004t0021 | 2 | HG01361.hp2 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1045_*1189del | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1045 | chr22 | 49902648 | ||||||
| chr22:49902667 | GGTGTGTG others(166): Show |
G | 5 | a0001c0002t0006 a0001c0002t0024 a0001c0008t0023 others(2): Show |
19 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*998_*1170del | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 998 | chr22 | 49902667 | ||||||
| chr22:49902678 | G | A | 1 | a0001c0002t0029 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1160C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1160 | chr22 | 49902678 | ||||||
| chr22:49902697 | A | G | 1 | a0001c0002t0029 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1141T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1141 | chr22 | 49902697 | ||||||
| chr22:49902700 | G | A | 1 | a0001c0002t0029 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1138C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1138 | chr22 | 49902700 | ||||||
| chr22:49902714 | ACTGTGTG others(138): Show |
A | 1 | a0002c0003t0058 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979_*1123del | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 979 | chr22 | 49902714 | ||||||
| chr22:49902715 | CTGTGTGT others(69): Show |
C | 1 | a0001c0002t0029 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1047_*1122delCCGT others(72): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 1047 | chr22 | 49902715 | ||||||
| chr22:49902844 | T | C | 1 | a0001c0001t0012 | 5 | HG00099.hp2 HG00323.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*994A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 994 | chr22 | 49902844 | ||||||
| chr22:49902924 | C | T | 1 | a0003c0007t0042 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*914G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 914 | chr22 | 49902924 | ||||||
| chr22:49902925 | G | A | 1 | a0001c0002t0024 | 2 | HG02559.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*913C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 913 | chr22 | 49902925 | ||||||
| chr22:49903028 | C | A | 1 | a0002c0003t0058 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 810 | chr22 | 49903028 | ||||||
| chr22:49903029 | A | G | 1 | a0002c0003t0058 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*809T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 809 | chr22 | 49903029 | ||||||
| chr22:49903070 | C | T | 2 | a0001c0004t0018 a0002c0003t0058 |
3 | HG00741.hp1 HG03710.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*768G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 768 | chr22 | 49903070 | ||||||
| chr22:49903105 | G | A | 2 | a0001c0001t0005 a0001c0001t0055 |
14 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*733C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 733 | chr22 | 49903105 | ||||||
| chr22:49903354 | G | T | 1 | a0002c0013t0028 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 484 | chr22 | 49903354 | ||||||
| chr22:49903386 | CCT | C | 6 | a0002c0003t0004 a0002c0003t0014 a0002c0003t0016 others(3): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451delAG | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 450 | chr22 | 49903386 | ||||||
| chr22:49903558 | C | T | 1 | a0001c0002t0008 | 9 | HG01243.hp2 HG02055.hp1 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*280G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 280 | chr22 | 49903558 | ||||||
| chr22:49903583 | A | G | 1 | a0001c0001t0041 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 255 | chr22 | 49903583 | ||||||
| chr22:49903598 | C | T | 5 | a0001c0002t0006 a0001c0002t0024 a0001c0008t0023 others(2): Show |
19 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*240G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 240 | chr22 | 49903598 | ||||||
| chr22:49903616 | G | A | 1 | a0001c0001t0056 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 222 | chr22 | 49903616 | ||||||
| chr22:49903643 | G | A | 1 | a0001c0002t0066 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 195 | chr22 | 49903643 | ||||||
| chr22:49903774 | C | A | 1 | a0001c0001t0057 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 64 | chr22 | 49903774 | ||||||
| chr22:49903787 | T | C | 49 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0007 others(46): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*51A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 51 | chr22 | 49903787 | ||||||
| chr22:49903805 | G | A | 1 | a0001c0001t0067 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 10/10 | 33 | chr22 | 49903805 | ||||||
| chr22:49918325 | A | G | 27 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(24): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-141T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/10 | 4560 | chr22 | 49918325 | ||||||
| chr22:49918341 | AAC | A | 27 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(24): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-159_-158delGT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/10 | 4577 | chr22 | 49918341 | ||||||
| chr22:49918387 | C | G | 2 | a0002c0003t0040 a0005c0016t0039 |
2 | HG02922.hp1 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-203G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/10 | 4622 | chr22 | 49918387 | ||||||
| chr22:49918387 | C | T | 26 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(23): Show |
96 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(93): Show |
5_prime_UTR_variant | MODIFIER | c.-203G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/10 | 4622 | chr22 | 49918387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49904109 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1239-43G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 9/9 | chr22 | 49904109 | |||||||
| chr22:49904273 | C | T | 1 | a0001c0002t0068g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1163-19G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 8/9 | chr22 | 49904273 | |||||||
| chr22:49904681 | C | T | 7 | a0001c0005t0013g0085 a0001c0005t0013g0086 a0001c0005t0013g0087 others(4): Show |
9 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.993-175G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49904681 | |||||||
| chr22:49904687 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.993-181A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49904687 | |||||||
| chr22:49904713 | C | T | 1 | a0001c0002t0065g0099 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.993-207G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49904713 | |||||||
| chr22:49905030 | G | A | 1 | a0002c0003t0014g0060 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.993-524C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905030 | |||||||
| chr22:49905169 | A | G | 1 | a0001c0010t0061g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.993-663T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905169 | |||||||
| chr22:49905170 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.993-664A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905170 | |||||||
| chr22:49905196 | G | A | 16 | a0001c0002t0010g0047 a0001c0002t0010g0048 a0001c0002t0010g0183 others(13): Show |
20 | HG01109.hp2 HG01256.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.993-690C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905196 | |||||||
| chr22:49905219 | T | C | 16 | a0001c0002t0010g0047 a0001c0002t0010g0048 a0001c0002t0010g0183 others(13): Show |
20 | HG01109.hp2 HG01256.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.993-713A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905219 | |||||||
| chr22:49905277 | C | G | 21 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(18): Show |
32 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.993-771G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905277 | |||||||
| chr22:49905340 | G | A | 1 | a0001c0004t0021g0027 | 2 | HG01361.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.993-834C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905340 | |||||||
| chr22:49905378 | T | A | 1 | a0001c0005t0013g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.993-872A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905378 | |||||||
| chr22:49905441 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.993-935G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905441 | |||||||
| chr22:49905526 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.993-1020C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905526 | |||||||
| chr22:49905939 | T | C | 101 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(98): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.993-1433A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905939 | |||||||
| chr22:49905951 | A | C | 2 | a0002c0003t0040g0097 a0005c0016t0039g0098 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.993-1445T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49905951 | |||||||
| chr22:49906144 | G | A | 1 | a0002c0003t0004g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.992+1577C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906144 | |||||||
| chr22:49906271 | C | T | 22 | a0001c0001t0001g0165 a0002c0003t0004g0007 a0002c0003t0004g0013 others(19): Show |
33 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.992+1450G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906271 | |||||||
| chr22:49906430 | A | G | 101 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(98): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.992+1291T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906430 | |||||||
| chr22:49906438 | C | T | 2 | a0002c0003t0026g0117 a0002c0003t0026g0166 |
2 | HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.992+1283G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906438 | |||||||
| chr22:49906453 | G | A | 1 | a0002c0003t0004g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.992+1268C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906453 | |||||||
| chr22:49906494 | G | A | 1 | a0001c0002t0003g0022 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.992+1227C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906494 | |||||||
| chr22:49906507 | G | A | 1 | a0001c0001t0041g0157 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.992+1214C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906507 | |||||||
| chr22:49906539 | G | A | 3 | a0001c0004t0009g0016 a0001c0004t0009g0094 a0001c0004t0009g0095 |
5 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.992+1182C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906539 | |||||||
| chr22:49906698 | G | A | 5 | a0001c0002t0010g0047 a0001c0002t0010g0048 a0001c0002t0010g0184 others(2): Show |
7 | HG01256.hp1 HG02040.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.992+1023C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906698 | |||||||
| chr22:49906790 | T | C | 106 | a0001c0001t0005g0019 a0001c0001t0005g0041 a0001c0001t0005g0155 others(103): Show |
153 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.992+931A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906790 | |||||||
| chr22:49906816 | C | T | 2 | a0001c0001t0002g0135 a0001c0001t0002g0148 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.992+905G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906816 | |||||||
| chr22:49906879 | G | A | 3 | a0001c0004t0009g0016 a0001c0004t0009g0094 a0001c0004t0009g0095 |
5 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.992+842C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906879 | |||||||
| chr22:49906914 | A | G | 81 | a0001c0001t0002g0045 a0001c0002t0003g0010 a0001c0002t0003g0021 others(78): Show |
118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.992+807T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49906914 | |||||||
| chr22:49907024 | C | T | 40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.992+697G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907024 | |||||||
| chr22:49907071 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.992+650G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907071 | |||||||
| chr22:49907234 | C | A | 2 | a0002c0003t0026g0117 a0002c0003t0026g0166 |
2 | HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.992+487G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907234 | |||||||
| chr22:49907347 | G | A | 17 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0111 others(14): Show |
23 | HG02040.hp2 HG02055.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.992+374C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907347 | |||||||
| chr22:49907491 | A | T | 1 | a0001c0002t0064g0181 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.992+230T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907491 | |||||||
| chr22:49907530 | C | T | 101 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(98): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.992+191G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907530 | |||||||
| chr22:49907551 | T | C | 1 | a0001c0008t0023g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.992+170A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907551 | |||||||
| chr22:49907601 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.992+120C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907601 | |||||||
| chr22:49907603 | C | T | 43 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(40): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.992+118G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907603 | |||||||
| chr22:49907692 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.992+29T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 7/9 | chr22 | 49907692 | |||||||
| chr22:49908016 | T | C | 70 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(67): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.769-72A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908016 | |||||||
| chr22:49908126 | C | T | 1 | a0003c0006t0006g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.769-182G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908126 | |||||||
| chr22:49908134 | G | C | 1 | a0001c0002t0007g0076 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.769-190C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908134 | |||||||
| chr22:49908147 | C | T | 3 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0148 |
3 | HG02683.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.769-203G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908147 | |||||||
| chr22:49908255 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | NA18953.hp1 NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.769-311G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908255 | |||||||
| chr22:49908307 | ATCACGAG others(45): Show |
A | 15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.769-415_769-364del others(52): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908307 | |||||||
| chr22:49908358 | TCTCTACT others(417): Show |
T | 40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.768+462_769-415del | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908358 | |||||||
| chr22:49908373 | CA | C | 15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.769-430delT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908373 | |||||||
| chr22:49908476 | C | T | 3 | a0001c0002t0006g0034 a0001c0002t0006g0111 a0001c0002t0024g0035 |
5 | HG02559.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.769-532G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908476 | |||||||
| chr22:49908526 | C | CA | 30 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0113 others(27): Show |
41 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.769-583dupT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908526 | |||||||
| chr22:49908526 | CA | C | 30 | a0001c0001t0001g0039 a0001c0001t0002g0135 a0001c0001t0002g0136 others(27): Show |
45 | HG01123.hp2 HG01168.hp2 HG01433.hp1 others(42): Show |
intron_variant | MODIFIER | c.769-583delT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908526 | |||||||
| chr22:49908548 | C | A | 1 | a0003c0007t0001g0036 | 2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.769-604G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908548 | |||||||
| chr22:49908567 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.769-623C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908567 | |||||||
| chr22:49908619 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.768+625C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908619 | |||||||
| chr22:49908622 | T | C | 18 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(15): Show |
29 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.768+622A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908622 | |||||||
| chr22:49908669 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0161 |
3 | HG01496.hp1 HG02083.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.768+575C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908669 | |||||||
| chr22:49908741 | C | T | 2 | a0002c0003t0026g0117 a0002c0003t0026g0166 |
2 | HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.768+503G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908741 | |||||||
| chr22:49908743 | A | G | 1 | a0001c0001t0005g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.768+501T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908743 | |||||||
| chr22:49908782 | C | T | 18 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(15): Show |
29 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.768+462G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908782 | |||||||
| chr22:49908821 | G | A | 18 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(15): Show |
29 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.768+423C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908821 | |||||||
| chr22:49908825 | G | A | 1 | a0001c0001t0005g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.768+419C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908825 | |||||||
| chr22:49908830 | T | C | 1 | a0001c0002t0008g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.768+414A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908830 | |||||||
| chr22:49908875 | C | T | 1 | a0001c0002t0011g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.768+369G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908875 | |||||||
| chr22:49908901 | A | G | 60 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(57): Show |
90 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.768+343T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908901 | |||||||
| chr22:49908951 | C | CA | 49 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0127 others(46): Show |
74 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.768+292dupT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908951 | |||||||
| chr22:49908951 | C | CAA | 18 | a0001c0002t0003g0092 a0001c0002t0010g0047 a0001c0002t0010g0048 others(15): Show |
22 | HG01109.hp2 HG01256.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.768+291_768+292dup others(2): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908951 | |||||||
| chr22:49908981 | G | A | 17 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0111 others(14): Show |
23 | HG02040.hp2 HG02055.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.768+263C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49908981 | |||||||
| chr22:49909023 | T | A | 16 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(13): Show |
27 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.768+221A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49909023 | |||||||
| chr22:49909202 | A | G | 101 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(98): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.768+42T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 6/9 | chr22 | 49909202 | |||||||
| chr22:49909376 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0124 others(7): Show |
21 | HG00639.hp1 HG01081.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.665-29G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909376 | |||||||
| chr22:49909440 | G | A | 9 | a0001c0002t0003g0021 a0001c0002t0003g0026 a0001c0002t0003g0063 others(6): Show |
12 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.665-93C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909440 | |||||||
| chr22:49909479 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.665-132A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909479 | |||||||
| chr22:49909487 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.665-140C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909487 | |||||||
| chr22:49909501 | G | C | 40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.665-154C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909501 | |||||||
| chr22:49909551 | G | A | 1 | a0001c0001t0001g0044 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.665-204C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909551 | |||||||
| chr22:49909598 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.665-251G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909598 | |||||||
| chr22:49909601 | G | A | 85 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(82): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.665-254C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909601 | |||||||
| chr22:49909717 | C | T | 2 | a0002c0003t0026g0117 a0002c0003t0026g0166 |
2 | HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.664+177G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909717 | |||||||
| chr22:49909867 | A | C | 65 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(62): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.664+27T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909867 | |||||||
| chr22:49909882 | T | C | 65 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(62): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.664+12A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909882 | |||||||
| chr22:49909885 | C | G | 65 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(62): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.664+9G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 5/9 | chr22 | 49909885 | |||||||
| chr22:49910233 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.470-145G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 4/9 | chr22 | 49910233 | |||||||
| chr22:49910338 | A | G | 2 | a0003c0006t0006g0105 a0003c0006t0006g0106 |
2 | NA18940.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.469+96T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 4/9 | chr22 | 49910338 | |||||||
| chr22:49910342 | C | T | 14 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(11): Show |
25 | HG00597.hp2 HG00642.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.469+92G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 4/9 | chr22 | 49910342 | |||||||
| chr22:49910343 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.469+91C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 4/9 | chr22 | 49910343 | |||||||
| chr22:49910420 | C | T | 1 | a0001c0001t0001g0017 | 3 | NA18950.hp2 NA18952.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.469+14G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 4/9 | chr22 | 49910420 | |||||||
| chr22:49910421 | G | A | 2 | a0001c0001t0001g0012 a0001c0012t0001g0130 |
6 | HG00544.hp2 HG02015.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.469+13C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 4/9 | chr22 | 49910421 | |||||||
| chr22:49910716 | G | A | 5 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(2): Show |
8 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-109C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49910716 | |||||||
| chr22:49910731 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG00140.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.296-124C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49910731 | |||||||
| chr22:49910943 | A | C | 100 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(97): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.296-336T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49910943 | |||||||
| chr22:49911100 | G | A | 1 | a0001c0004t0018g0028 | 2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.296-493C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911100 | |||||||
| chr22:49911157 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
14 | HG02083.hp1 HG02155.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.296-550C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911157 | |||||||
| chr22:49911287 | C | A | 17 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0111 others(14): Show |
23 | HG02040.hp2 HG02055.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.296-680G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911287 | |||||||
| chr22:49911339 | G | A | 1 | a0002c0003t0040g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.296-732C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911339 | |||||||
| chr22:49911434 | C | T | 2 | a0002c0003t0026g0117 a0002c0003t0026g0166 |
2 | HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.296-827G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911434 | |||||||
| chr22:49911436 | T | C | 1 | a0001c0002t0027g0049 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.296-829A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911436 | |||||||
| chr22:49911445 | T | C | 1 | a0005c0016t0039g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.296-838A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911445 | |||||||
| chr22:49911445 | TC | T | 22 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(19): Show |
37 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.296-839delG | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911445 | |||||||
| chr22:49911446 | C | T | 1 | a0002c0013t0028g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.296-839G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911446 | |||||||
| chr22:49911450 | T | A | 23 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(20): Show |
38 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.296-843A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911450 | |||||||
| chr22:49911465 | C | T | 7 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(4): Show |
11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.296-858G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911465 | |||||||
| chr22:49911488 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.296-881C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911488 | |||||||
| chr22:49911504 | G | A | 1 | a0001c0010t0061g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.296-897C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911504 | |||||||
| chr22:49911584 | G | A | 2 | a0004c0009t0022g0108 a0004c0009t0022g0109 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.296-977C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911584 | |||||||
| chr22:49911596 | G | C | 15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.296-989C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911596 | |||||||
| chr22:49911643 | A | G | 1 | a0001c0002t0008g0073 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.296-1036T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911643 | |||||||
| chr22:49911678 | C | T | 2 | a0002c0003t0040g0097 a0005c0016t0039g0098 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.296-1071G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911678 | |||||||
| chr22:49911714 | G | A | 15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.296-1107C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911714 | |||||||
| chr22:49911777 | G | T | 1 | a0001c0002t0068g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-1170C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911777 | |||||||
| chr22:49911813 | T | G | 36 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0111 others(33): Show |
46 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.296-1206A>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911813 | |||||||
| chr22:49911854 | C | T | 1 | a0002c0003t0038g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.296-1247G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911854 | |||||||
| chr22:49911867 | T | C | 42 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(39): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.296-1260A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911867 | |||||||
| chr22:49911920 | A | AATGCCCA others(14): Show |
1 | a0004c0009t0022g0108 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.296-1334_296-1314d others(23): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911920 | |||||||
| chr22:49911984 | T | TGCGGGAT others(65): Show |
31 | a0001c0002t0006g0033 a0001c0002t0010g0047 a0001c0002t0010g0048 others(28): Show |
39 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(36): Show |
intron_variant | MODIFIER | c.295+1329_296-1378d others(74): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911984 | |||||||
| chr22:49911984 | T | TGTGGGAT others(65): Show |
15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.296-1378_296-1377i others(74): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49911984 | |||||||
| chr22:49912003 | C | CCGGGATC others(65): Show |
1 | a0002c0003t0040g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.295+1381_295+1382i others(74): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912003 | |||||||
| chr22:49912021 | A | ACGGGATC others(65): Show |
8 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(5): Show |
12 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+1363_295+1364i others(74): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912021 | |||||||
| chr22:49912021 | A | ACGGGATC others(65): Show |
2 | a0004c0009t0022g0108 a0004c0009t0022g0109 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.295+1363_295+1364i others(74): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912021 | |||||||
| chr22:49912021 | A | C | 15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.295+1364T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912021 | |||||||
| chr22:49912041 | G | GGGATCAG others(65): Show |
3 | a0001c0002t0006g0034 a0001c0002t0006g0111 a0001c0002t0024g0035 |
5 | HG02559.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1343_295+1344i others(74): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912041 | |||||||
| chr22:49912058 | C | CGGGATCA others(65): Show |
1 | a0001c0002t0010g0184 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.295+1326_295+1327i others(74): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912058 | |||||||
| chr22:49912066 | G | C | 40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.295+1319C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912066 | |||||||
| chr22:49912069 | T | TCGGCCCC others(12): Show |
40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.295+1315_295+1316i others(21): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912069 | |||||||
| chr22:49912074 | C | A | 39 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(36): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.295+1311G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912074 | |||||||
| chr22:49912074 | C | G | 1 | a0001c0005t0013g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.295+1311G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912074 | |||||||
| chr22:49912076 | G | A | 23 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(20): Show |
38 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.295+1309C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912076 | |||||||
| chr22:49912101 | C | G | 40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.295+1284G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912101 | |||||||
| chr22:49912110 | C | G | 40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.295+1275G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912110 | |||||||
| chr22:49912221 | G | C | 1 | a0001c0002t0010g0184 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.295+1164C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912221 | |||||||
| chr22:49912339 | C | T | 1 | a0001c0002t0010g0047 | 2 | HG02040.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.295+1046G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912339 | |||||||
| chr22:49912369 | A | T | 3 | a0001c0002t0025g0030 a0001c0002t0059g0102 a0001c0002t0060g0103 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+1016T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912369 | |||||||
| chr22:49912416 | G | A | 1 | a0001c0002t0003g0072 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.295+969C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912416 | |||||||
| chr22:49912431 | C | T | 7 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(4): Show |
11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.295+954G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912431 | |||||||
| chr22:49912579 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.295+806A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912579 | |||||||
| chr22:49912612 | C | T | 2 | a0001c0002t0003g0067 a0001c0002t0065g0099 |
2 | NA18965.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.295+773G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912612 | |||||||
| chr22:49912618 | A | C | 2 | a0001c0002t0003g0067 a0001c0002t0065g0099 |
2 | NA18965.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.295+767T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912618 | |||||||
| chr22:49912668 | C | T | 63 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(60): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.295+717G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912668 | |||||||
| chr22:49912669 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.295+716C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912669 | |||||||
| chr22:49912690 | G | A | 23 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(20): Show |
38 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.295+695C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912690 | |||||||
| chr22:49912873 | G | GA | 15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.295+511dupT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912873 | |||||||
| chr22:49912876 | A | G | 1 | a0001c0002t0011g0180 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.295+509T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912876 | |||||||
| chr22:49912885 | G | A | 3 | a0002c0003t0040g0097 a0002c0003t0058g0177 a0005c0016t0039g0098 |
3 | HG00741.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.295+500C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49912885 | |||||||
| chr22:49913093 | G | A | 15 | a0001c0002t0010g0047 a0001c0002t0010g0048 a0001c0002t0010g0183 others(12): Show |
19 | HG01256.hp1 HG01884.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.295+292C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49913093 | |||||||
| chr22:49913096 | G | A | 1 | a0002c0003t0038g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.295+289C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49913096 | |||||||
| chr22:49913199 | G | A | 2 | a0001c0005t0013g0087 a0001c0005t0032g0088 |
2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.295+186C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49913199 | |||||||
| chr22:49913234 | G | T | 1 | a0001c0012t0001g0130 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.295+151C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49913234 | |||||||
| chr22:49913292 | C | T | 55 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(52): Show |
87 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+93G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49913292 | |||||||
| chr22:49913315 | G | A | 2 | a0002c0003t0026g0117 a0002c0003t0026g0166 |
2 | HG03688.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.295+70C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49913315 | |||||||
| chr22:49913320 | C | T | 1 | a0001c0002t0003g0066 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.295+65G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49913320 | |||||||
| chr22:49913321 | G | A | 22 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(19): Show |
37 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.295+64C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 3/9 | chr22 | 49913321 | |||||||
| chr22:49913536 | G | T | 16 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(13): Show |
27 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.163-19C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 2/9 | chr22 | 49913536 | |||||||
| chr22:49913548 | G | C | 1 | a0001c0001t0067g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.163-31C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 2/9 | chr22 | 49913548 | |||||||
| chr22:49913581 | CA | C | 3 | a0001c0002t0025g0030 a0001c0002t0059g0102 a0001c0002t0060g0103 |
4 | HG02055.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+22delT | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 2/9 | chr22 | 49913581 | |||||||
| chr22:49913886 | T | C | 7 | a0002c0003t0004g0013 a0002c0003t0004g0054 a0002c0003t0004g0058 others(4): Show |
10 | HG00438.hp2 HG00597.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.-78-43A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49913886 | |||||||
| chr22:49914080 | T | A | 1 | a0001c0004t0018g0028 | 2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-78-237A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914080 | |||||||
| chr22:49914155 | C | T | 1 | a0001c0002t0059g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-78-312G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914155 | |||||||
| chr22:49914225 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-78-382C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914225 | |||||||
| chr22:49914239 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-78-396T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914239 | |||||||
| chr22:49914248 | A | G | 101 | a0001c0001t0001g0129 a0001c0002t0003g0010 a0001c0002t0003g0021 others(98): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-78-405T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914248 | |||||||
| chr22:49914284 | T | C | 63 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(60): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-78-441A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914284 | |||||||
| chr22:49914297 | C | T | 11 | a0001c0002t0006g0033 a0001c0008t0023g0100 a0001c0008t0023g0101 others(8): Show |
14 | HG02040.hp2 HG02257.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-78-454G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914297 | |||||||
| chr22:49914397 | C | T | 1 | a0006c0018t0062g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-78-554G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914397 | |||||||
| chr22:49914406 | C | T | 8 | a0001c0002t0003g0010 a0001c0002t0003g0064 a0001c0002t0003g0066 others(5): Show |
12 | HG00423.hp2 HG02071.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.-78-563G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914406 | |||||||
| chr22:49914447 | T | TC | 5 | a0001c0002t0011g0050 a0001c0002t0011g0185 a0001c0002t0011g0186 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78-605dupG | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914447 | |||||||
| chr22:49914502 | G | C | 2 | a0001c0001t0005g0019 a0001c0001t0005g0168 |
4 | HG02109.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-659C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914502 | |||||||
| chr22:49914552 | G | A | 1 | a0001c0002t0047g0174 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-78-709C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914552 | |||||||
| chr22:49914742 | A | C | 5 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG03669.hp2 NA18953.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78-899T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914742 | |||||||
| chr22:49914744 | T | A | 1 | a0001c0001t0001g0169 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-78-901A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914744 | |||||||
| chr22:49914781 | G | C | 1 | a0001c0010t0061g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-78-938C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914781 | |||||||
| chr22:49914789 | G | A | 15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-78-946C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914789 | |||||||
| chr22:49914796 | A | C | 37 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0111 others(34): Show |
47 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(44): Show |
intron_variant | MODIFIER | c.-78-953T>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914796 | |||||||
| chr22:49914797 | G | A | 37 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0111 others(34): Show |
47 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(44): Show |
intron_variant | MODIFIER | c.-78-954C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914797 | |||||||
| chr22:49914949 | G | A | 26 | a0001c0002t0006g0034 a0001c0002t0006g0111 a0001c0002t0024g0035 others(23): Show |
43 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-78-1106C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49914949 | |||||||
| chr22:49915008 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-78-1165G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49915008 | |||||||
| chr22:49915240 | G | A | 7 | a0001c0005t0013g0085 a0001c0005t0013g0086 a0001c0005t0013g0087 others(4): Show |
9 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.-78-1397C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49915240 | |||||||
| chr22:49915440 | C | T | 22 | a0001c0001t0056g0122 a0001c0002t0003g0010 a0001c0002t0003g0021 others(19): Show |
30 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.-78-1597G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49915440 | |||||||
| chr22:49915449 | C | G | 3 | a0002c0003t0040g0097 a0002c0003t0058g0177 a0005c0016t0039g0098 |
3 | HG00741.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-78-1606G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49915449 | |||||||
| chr22:49915467 | G | A | 1 | a0002c0003t0058g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-78-1624C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49915467 | |||||||
| chr22:49915486 | G | A | 1 | a0002c0003t0040g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-78-1643C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49915486 | |||||||
| chr22:49915587 | T | A | 108 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0045 others(105): Show |
163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.-78-1744A>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49915587 | |||||||
| chr22:49915798 | G | A | 63 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(60): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-78-1955C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49915798 | |||||||
| chr22:49916055 | C | T | 2 | a0001c0008t0023g0100 a0001c0008t0023g0101 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-79+2208G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916055 | |||||||
| chr22:49916218 | A | G | 1 | a0001c0001t0002g0037 | 2 | HG02015.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-79+2045T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916218 | |||||||
| chr22:49916259 | A | T | 7 | a0001c0005t0013g0085 a0001c0005t0013g0086 a0001c0005t0013g0087 others(4): Show |
9 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.-79+2004T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916259 | |||||||
| chr22:49916263 | A | T | 40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.-79+2000T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916263 | |||||||
| chr22:49916267 | A | T | 81 | a0001c0001t0001g0120 a0001c0001t0002g0121 a0001c0002t0003g0010 others(78): Show |
118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-79+1996T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916267 | |||||||
| chr22:49916349 | G | C | 23 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(20): Show |
38 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.-79+1914C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916349 | |||||||
| chr22:49916398 | T | C | 63 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(60): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-79+1865A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916398 | |||||||
| chr22:49916551 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-79+1712C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916551 | |||||||
| chr22:49916606 | G | A | 3 | a0001c0002t0006g0034 a0001c0002t0006g0111 a0001c0002t0024g0035 |
5 | HG02559.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-79+1657C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916606 | |||||||
| chr22:49916762 | G | A | 40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.-79+1501C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916762 | |||||||
| chr22:49916806 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-79+1457G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916806 | |||||||
| chr22:49916817 | G | A | 1 | a0002c0003t0026g0117 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-79+1446C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916817 | |||||||
| chr22:49916952 | G | A | 23 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(20): Show |
38 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.-79+1311C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916952 | |||||||
| chr22:49916973 | G | A | 1 | a0001c0001t0002g0046 | 2 | HG00609.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-79+1290C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49916973 | |||||||
| chr22:49917015 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-79+1248G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917015 | |||||||
| chr22:49917136 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-79+1127G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917136 | |||||||
| chr22:49917181 | A | G | 63 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(60): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-79+1082T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917181 | |||||||
| chr22:49917199 | G | T | 63 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(60): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-79+1064C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917199 | |||||||
| chr22:49917232 | T | C | 63 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(60): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-79+1031A>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917232 | |||||||
| chr22:49917234 | C | T | 63 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(60): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-79+1029G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917234 | |||||||
| chr22:49917271 | A | G | 8 | a0001c0008t0023g0100 a0001c0008t0023g0101 a0003c0006t0006g0031 others(5): Show |
10 | HG02040.hp2 HG03017.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.-79+992T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917271 | |||||||
| chr22:49917298 | A | G | 1 | a0002c0003t0004g0054 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-79+965T>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917298 | |||||||
| chr22:49917428 | TG | T | 7 | a0001c0005t0013g0085 a0001c0005t0013g0086 a0001c0005t0013g0087 others(4): Show |
9 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.-79+834delC | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917428 | |||||||
| chr22:49917468 | C | T | 4 | a0001c0002t0025g0030 a0001c0002t0059g0102 a0001c0002t0060g0103 others(1): Show |
5 | HG02055.hp2 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+795G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917468 | |||||||
| chr22:49917496 | C | A | 1 | a0001c0001t0044g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-79+767G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917496 | |||||||
| chr22:49917500 | G | C | 1 | a0001c0001t0044g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-79+763C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917500 | |||||||
| chr22:49917501 | T | G | 1 | a0001c0001t0044g0176 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-79+762A>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917501 | |||||||
| chr22:49917558 | C | T | 15 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(12): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-79+705G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917558 | |||||||
| chr22:49917643 | G | T | 1 | a0002c0003t0058g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-79+620C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917643 | |||||||
| chr22:49917656 | A | T | 1 | a0002c0003t0058g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-79+607T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917656 | |||||||
| chr22:49917705 | C | CT | 23 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0002t0006g0033 others(20): Show |
28 | HG00741.hp1 HG00741.hp2 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.-79+557dupA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917705 | |||||||
| chr22:49917705 | C | CTTTTTTT others(2): Show |
15 | a0001c0002t0003g0063 a0001c0002t0003g0080 a0001c0002t0003g0091 others(12): Show |
19 | HG00140.hp1 HG01074.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.-79+549_-79+557dup others(9): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917705 | |||||||
| chr22:49917705 | C | CTTTTTTT others(3): Show |
40 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(37): Show |
70 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-79+548_-79+557dup others(10): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917705 | |||||||
| chr22:49917705 | C | CTTTTTTT others(4): Show |
6 | a0001c0002t0003g0064 a0001c0002t0008g0065 a0001c0002t0008g0084 others(3): Show |
6 | HG02572.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-79+547_-79+557dup others(11): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917705 | |||||||
| chr22:49917719 | A | T | 25 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(22): Show |
40 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-79+544T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917719 | |||||||
| chr22:49917809 | C | A | 1 | a0001c0002t0008g0084 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-79+454G>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917809 | |||||||
| chr22:49917821 | G | T | 2 | a0001c0002t0003g0021 a0001c0002t0003g0063 |
3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-79+442C>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917821 | |||||||
| chr22:49917822 | A | T | 2 | a0001c0002t0003g0021 a0001c0002t0003g0063 |
3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-79+441T>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917822 | |||||||
| chr22:49917825 | A | AT | 33 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(30): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.-79+437dupA | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917825 | |||||||
| chr22:49917930 | C | CCCCCAGG others(12): Show |
1 | a0001c0001t0045g0112 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-79+314_-79+332dup others(19): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917930 | |||||||
| chr22:49917931 | C | T | 18 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0111 others(15): Show |
24 | HG02040.hp2 HG02055.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-79+332G>A | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917931 | |||||||
| chr22:49917934 | C | G | 8 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(5): Show |
12 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-79+329G>C | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917934 | |||||||
| chr22:49917945 | TCCGGCCC others(12): Show |
T | 1 | a0001c0001t0002g0029 | 2 | HG00438.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-79+299_-79+317del others(19): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917945 | |||||||
| chr22:49917948 | G | A | 37 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0111 others(34): Show |
54 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.-79+315C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917948 | |||||||
| chr22:49917967 | G | A | 1 | a0002c0003t0058g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-79+296C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917967 | |||||||
| chr22:49917986 | A | AGCCCCAG others(164): Show |
1 | a0002c0003t0038g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-79+276_-79+277ins others(171): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917986 | |||||||
| chr22:49917986 | A | AGCCCCAG others(183): Show |
13 | a0002c0003t0004g0007 a0002c0003t0004g0013 a0002c0003t0004g0054 others(10): Show |
24 | HG00438.hp2 HG00642.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-79+276_-79+277ins others(190): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917986 | |||||||
| chr22:49917986 | A | AGCCCCAG others(164): Show |
1 | a0002c0003t0004g0062 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-79+276_-79+277ins others(171): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917986 | |||||||
| chr22:49917986 | A | AGCCCCAG others(183): Show |
1 | a0002c0013t0028g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-79+276_-79+277ins others(190): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917986 | |||||||
| chr22:49917986 | A | AGCCCCAG others(164): Show |
7 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(4): Show |
11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-79+276_-79+277ins others(171): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917986 | |||||||
| chr22:49917986 | A | AGCCCCAG others(164): Show |
1 | a0001c0002t0003g0010 | 5 | HG00423.hp2 HG02080.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+276_-79+277ins others(171): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917986 | |||||||
| chr22:49917986 | A | AGCCCCAG others(164): Show |
36 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0063 others(33): Show |
50 | HG00099.hp1 HG00140.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-79+276_-79+277ins others(171): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917986 | |||||||
| chr22:49917993 | G | GGTGAGAG others(164): Show |
2 | a0001c0002t0003g0026 a0001c0002t0003g0091 |
3 | HG00323.hp2 HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-79+269_-79+270ins others(171): Show |
ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49917993 | |||||||
| chr22:49918054 | G | A | 1 | a0001c0002t0003g0092 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-79+209C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49918054 | |||||||
| chr22:49918078 | G | A | 39 | a0001c0002t0003g0010 a0001c0002t0003g0021 a0001c0002t0003g0022 others(36): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.-79+185C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49918078 | |||||||
| chr22:49918138 | G | C | 7 | a0001c0004t0009g0016 a0001c0004t0009g0093 a0001c0004t0009g0094 others(4): Show |
11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-79+125C>G | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49918138 | |||||||
| chr22:49918145 | G | A | 15 | a0001c0002t0010g0047 a0001c0002t0010g0048 a0001c0002t0010g0183 others(12): Show |
19 | HG01109.hp2 HG01256.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-79+118C>T | ALG12 | ENSG00000182858.14 | transcript | ENST00000330817.11 | protein_coding | 1/9 | chr22 | 49918145 |