Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29099 |
| ensemblid | ENSG00000110442.12 |
| hgncid | 25014 |
| symbol | COMMD9 |
| name | COMM domain containing 9 |
| refseq_nuc | NM_014186.4 |
| refseq_prot | NP_054905.2 |
| ensembl_nuc | ENST00000263401.10 |
| ensembl_prot | ENSP00000263401.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 36272292 |
| end | 36289424 |
| strand | - |
| ver | v1.2 |
| region | chr11:36272292-36289424 |
| region5000 | chr11:36267292-36294424 |
| regionname0 | COMMD9_chr11_36272292_36289424 |
| regionname5000 | COMMD9_chr11_36267292_36294424 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 198 | 443 | 92 | 79 | 212 | 16 | 42 | 166 | COMMD9_chr11_36267292_36294424 | COMMD9 | MAALT others(193): Show |
chr11 | 36267292 | 36294424 |
| a0002 | 0/0 | 198 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | MAALT others(193): Show |
chr11 | 36267292 | 36294424 |
| a0003 | 0/0 | 198 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | MAALT others(193): Show |
chr11 | 36267292 | 36294424 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 594 | 440 | 91 | 79 | 212 | 15 | 41 | COMMD9_chr11_36267292_36294424 | COMMD9 | ATGGC others(589): Show |
chr11 | 36267292 | 36294424 | ||
| a0001c0004 | 0/0 | 594 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | ATGGC others(589): Show |
chr11 | 36267292 | 36294424 | ||
| a0001c0005 | 0/0 | 594 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | ATGGC others(589): Show |
chr11 | 36267292 | 36294424 | ||
| a0001c0006 | 0/0 | 594 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | ATGGC others(589): Show |
chr11 | 36267292 | 36294424 | ||
| a0002c0002 | 0/0 | 594 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | ATGGC others(589): Show |
chr11 | 36267292 | 36294424 | ||
| a0003c0003 | 0/0 | 594 | 2 | 1 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | ATGGC others(589): Show |
chr11 | 36267292 | 36294424 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2949 | 231 | 40 | 51 | 100 | 10 | 29 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0002 | 0/0 | 2949 | 89 | 21 | 6 | 55 | 2 | 5 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0003 | 0/0 | 2949 | 47 | 9 | 7 | 31 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0004 | 0/0 | 2943 | 34 | 0 | 12 | 21 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2938): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0005 | 0/0 | 2949 | 15 | 4 | 1 | 2 | 2 | 6 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0006 | 0/0 | 2949 | 5 | 5 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0007 | 0/0 | 2949 | 4 | 4 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0008 | 0/0 | 2949 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0009 | 1/0 | 2949 | 3 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0010 | 0/0 | 2949 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0011 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0012 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0013 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2934): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0014 | 0/0 | 2949 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0015 | 0/0 | 2949 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0016 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0001t0017 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0004t0007 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0005t0001 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0001c0006t0001 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0002c0002t0006 | 0/0 | 2949 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| a0003c0003t0005 | 0/0 | 2949 | 2 | 1 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | GACTT others(2944): Show |
chr11 | 36267292 | 36294424 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0063 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0064 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0066 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0001 | 0/0 | 27 | 1 | 1 | 24 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0002 | 0/0 | 14 | 0 | 3 | 11 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0015 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0016 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0065 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0007g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0008g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0009g0025 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0014g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0015g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0016g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0001t0017g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0004t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0001c0006t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0002c0002t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0002c0002t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0002c0002t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0003c0003t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| a0003c0003t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0015 | EUR | GBR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00099 | hp2 | a0001 | c0006 | t0001 | g0140 | EUR | GBR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | FIN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | FIN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0021 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0117 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0272 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01109 | hp1 | a0003 | c0003 | t0005 | g0067 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01975 | hp1 | a0001 | c0001 | t0015 | g0222 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02145 | hp2 | a0001 | c0001 | t0013 | g0148 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CDX | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02602 | hp2 | a0001 | c0001 | t0017 | g0277 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02615 | hp1 | a0002 | c0002 | t0006 | g0072 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02615 | hp2 | a0003 | c0003 | t0005 | g0068 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0025 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0108 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0110 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0111 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02886 | hp2 | a0001 | c0001 | t0016 | g0208 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0154 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02965 | hp2 | a0001 | c0004 | t0007 | g0155 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0249 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0174 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0025 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0245 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03516 | hp2 | a0002 | c0002 | t0006 | g0073 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0109 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0038 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0114 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03942 | hp2 | a0001 | c0005 | t0001 | g0193 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0112 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | CHB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18906 | hp1 | a0002 | c0002 | t0006 | g0071 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18967 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ASW | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ASW | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | TSI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0107 | EUR | TSI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0038 | EUR | TSI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | GIH | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01123 | hp1 | a0001 | c0001 | t0014 | g0146 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0100 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | USA | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | USA | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | USA | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0214 | REF | REF | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0025 | REF | REF | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:36276183 | T | A | 1 | a0003 | 2 | HG01109.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.410A>T | p.Asp137Val | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/6 | 422/2949 | 410/597 | 137/198 | chr11 | 36276183 | |||
| chr11:36277107 | C | T | 1 | a0002 | 3 | HG02615.hp1 HG03516.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.334G>A | p.Glu112Lys | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/6 | 346/2949 | 334/597 | 112/198 | chr11 | 36277107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:36274647 | G | A | 1 | a0001c0004 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.582C>T | p.Ala194Ala | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 594/2949 | 582/597 | 194/198 | chr11 | 36274647 | |||
| chr11:36276161 | G | A | 1 | a0001c0005 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.432C>T | p.Val144Val | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/6 | 444/2949 | 432/597 | 144/198 | chr11 | 36276161 | |||
| chr11:36278557 | G | A | 1 | a0001c0006 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.237C>T | p.Ala79Ala | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/6 | 249/2949 | 237/597 | 79/198 | chr11 | 36278557 | |||
| chr11:36289362 | C | T | 1 | a0003c0003 | 2 | HG01109.hp1 HG02615.hp2 |
splice_region_variant&synonymous_variant | LOW | c.51G>A | p.Lys17Lys | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/6 | 63/2949 | 51/597 | 17/198 | chr11 | 36289362 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:36272484 | C | G | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(4): Show |
115 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2148G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2148 | chr11 | 36272484 | ||||||
| chr11:36272502 | A | G | 4 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(1): Show |
97 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2130T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2130 | chr11 | 36272502 | ||||||
| chr11:36272556 | TGGAGGGT others(3): Show |
T | 1 | a0001c0001t0013 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2066_*2075delCATA others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2066 | chr11 | 36272556 | ||||||
| chr11:36272567 | A | T | 1 | a0001c0001t0013 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2065 | chr11 | 36272567 | ||||||
| chr11:36272572 | G | C | 1 | a0001c0001t0014 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2060C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2060 | chr11 | 36272572 | ||||||
| chr11:36272689 | T | G | 2 | a0001c0001t0007 a0001c0004t0007 |
5 | HG02451.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1943A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1943 | chr11 | 36272689 | ||||||
| chr11:36272830 | G | A | 3 | a0001c0001t0005 a0001c0001t0012 a0003c0003t0005 |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1802C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1802 | chr11 | 36272830 | ||||||
| chr11:36273368 | C | T | 1 | a0001c0001t0003 | 47 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1264G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1264 | chr11 | 36273368 | ||||||
| chr11:36273378 | G | A | 2 | a0001c0001t0005 a0003c0003t0005 |
17 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1254C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1254 | chr11 | 36273378 | ||||||
| chr11:36273404 | A | T | 3 | a0001c0001t0005 a0001c0001t0012 a0003c0003t0005 |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1228T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1228 | chr11 | 36273404 | ||||||
| chr11:36273484 | ATTTATT | A | 1 | a0001c0001t0004 | 34 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1142_*1147delAATA others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1142 | chr11 | 36273484 | ||||||
| chr11:36273534 | T | G | 1 | a0001c0001t0015 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1098A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1098 | chr11 | 36273534 | ||||||
| chr11:36273544 | C | T | 1 | a0001c0001t0010 | 2 | HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1088G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1088 | chr11 | 36273544 | ||||||
| chr11:36273607 | G | A | 1 | a0001c0001t0016 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1025C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1025 | chr11 | 36273607 | ||||||
| chr11:36273635 | C | T | 3 | a0001c0001t0005 a0001c0001t0012 a0003c0003t0005 |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*997G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 997 | chr11 | 36273635 | ||||||
| chr11:36273706 | T | G | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(3): Show |
105 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*926A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 926 | chr11 | 36273706 | ||||||
| chr11:36273773 | T | C | 1 | a0001c0001t0017 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*859A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 859 | chr11 | 36273773 | ||||||
| chr11:36273982 | G | T | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(17): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
3_prime_UTR_variant | MODIFIER | c.*650C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 650 | chr11 | 36273982 | ||||||
| chr11:36274361 | C | T | 1 | a0001c0001t0011 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 271 | chr11 | 36274361 | ||||||
| chr11:36274431 | A | T | 1 | a0001c0001t0008 | 3 | HG00597.hp1 NA18939.hp2 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*201T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 201 | chr11 | 36274431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:36274864 | C | T | 1 | a0001c0001t0001g0062 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.457-92G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36274864 | |||||||
| chr11:36274988 | A | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0241 others(1): Show |
4 | HG02717.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.457-216T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36274988 | |||||||
| chr11:36275091 | T | C | 1 | a0001c0001t0017g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.457-319A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275091 | |||||||
| chr11:36275418 | C | T | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.457-646G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275418 | |||||||
| chr11:36275446 | C | CT | 50 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.457-675dupA | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275446 | |||||||
| chr11:36275446 | CT | C | 97 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
138 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.457-675delA | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275446 | |||||||
| chr11:36275470 | AGTCT | A | 40 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0051 others(37): Show |
49 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.456+663_456+666del others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275470 | |||||||
| chr11:36275476 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0137 |
3 | HG03239.hp1 HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.456+661T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275476 | |||||||
| chr11:36275513 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.456+624C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275513 | |||||||
| chr11:36275519 | C | T | 1 | a0001c0001t0015g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.456+618G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275519 | |||||||
| chr11:36275600 | C | T | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.456+537G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275600 | |||||||
| chr11:36275605 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.456+532C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275605 | |||||||
| chr11:36275632 | T | C | 40 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(37): Show |
68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.456+505A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275632 | |||||||
| chr11:36275635 | G | T | 1 | a0001c0001t0004g0168 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.456+502C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275635 | |||||||
| chr11:36275784 | GCCTAATC others(1): Show |
G | 24 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0028 others(21): Show |
34 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.456+345_456+352del others(8): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275784 | |||||||
| chr11:36275856 | CACT | C | 3 | a0001c0001t0001g0176 a0001c0001t0003g0026 a0001c0001t0003g0175 |
5 | HG02559.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.456+278_456+280del others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275856 | |||||||
| chr11:36276480 | A | C | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.353-240T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276480 | |||||||
| chr11:36276551 | C | G | 140 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
209 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.353-311G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276551 | |||||||
| chr11:36276558 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.353-318T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276558 | |||||||
| chr11:36276641 | T | C | 100 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.353-401A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276641 | |||||||
| chr11:36276647 | C | T | 40 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0051 others(37): Show |
49 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.353-407G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276647 | |||||||
| chr11:36276739 | G | T | 3 | a0001c0001t0001g0176 a0001c0001t0003g0026 a0001c0001t0003g0175 |
5 | HG02559.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.352+350C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276739 | |||||||
| chr11:36276814 | T | A | 1 | a0001c0001t0001g0255 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.352+275A>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276814 | |||||||
| chr11:36276877 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.352+212G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276877 | |||||||
| chr11:36276939 | A | C | 4 | a0001c0001t0002g0037 a0001c0001t0002g0091 a0001c0001t0002g0097 others(1): Show |
5 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.352+150T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276939 | |||||||
| chr11:36277005 | C | T | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.352+84G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36277005 | |||||||
| chr11:36277024 | G | C | 3 | a0001c0001t0002g0012 a0001c0001t0002g0032 a0001c0001t0002g0075 |
7 | HG01891.hp2 HG02257.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+65C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36277024 | |||||||
| chr11:36277052 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.352+37G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36277052 | |||||||
| chr11:36277328 | G | C | 40 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(37): Show |
68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.318-205C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277328 | |||||||
| chr11:36277380 | C | A | 40 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(37): Show |
68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.318-257G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277380 | |||||||
| chr11:36277414 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318-291T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277414 | |||||||
| chr11:36277701 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0202 others(3): Show |
8 | HG02257.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-578G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277701 | |||||||
| chr11:36277729 | G | GA | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.318-607dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277729 | |||||||
| chr11:36277818 | A | AT | 40 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(37): Show |
68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+658dupA | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277818 | |||||||
| chr11:36277828 | T | G | 40 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(37): Show |
68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+649A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277828 | |||||||
| chr11:36277878 | G | A | 24 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0028 others(21): Show |
34 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.317+599C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277878 | |||||||
| chr11:36278024 | T | C | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.317+453A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278024 | |||||||
| chr11:36278098 | C | A | 1 | a0001c0001t0003g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.317+379G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278098 | |||||||
| chr11:36278154 | G | C | 40 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(37): Show |
68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+323C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278154 | |||||||
| chr11:36278217 | C | T | 97 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
138 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.317+260G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278217 | |||||||
| chr11:36278267 | AG | A | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.317+209delC | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278267 | |||||||
| chr11:36278426 | A | T | 46 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0051 others(43): Show |
56 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.317+51T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278426 | |||||||
| chr11:36278623 | G | C | 1 | a0001c0001t0005g0115 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.178-7C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278623 | |||||||
| chr11:36278629 | C | T | 1 | a0001c0001t0007g0154 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178-13G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278629 | |||||||
| chr11:36278661 | G | A | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-45C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278661 | |||||||
| chr11:36278680 | G | A | 24 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(21): Show |
50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.178-64C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278680 | |||||||
| chr11:36278821 | G | T | 40 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0051 others(37): Show |
49 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.178-205C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278821 | |||||||
| chr11:36278834 | C | G | 273 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.178-218G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278834 | |||||||
| chr11:36279016 | G | C | 273 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.178-400C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279016 | |||||||
| chr11:36279031 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0127 |
7 | HG01261.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-415C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279031 | |||||||
| chr11:36279052 | G | T | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-436C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279052 | |||||||
| chr11:36279074 | A | G | 1 | a0001c0001t0001g0062 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.178-458T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279074 | |||||||
| chr11:36279124 | C | T | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-508G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279124 | |||||||
| chr11:36279125 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
12 | HG01261.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-509C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279125 | |||||||
| chr11:36279243 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178-627C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279243 | |||||||
| chr11:36279285 | C | T | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.178-669G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279285 | |||||||
| chr11:36279615 | A | T | 78 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.178-999T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279615 | |||||||
| chr11:36279630 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.178-1014G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279630 | |||||||
| chr11:36279674 | T | C | 24 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(21): Show |
50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.177+1038A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279674 | |||||||
| chr11:36279676 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.177+1036C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279676 | |||||||
| chr11:36279738 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.177+974T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279738 | |||||||
| chr11:36279824 | G | C | 5 | a0001c0001t0006g0098 a0001c0001t0006g0099 a0001c0001t0006g0100 others(2): Show |
5 | HG02109.hp1 HG02976.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+888C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279824 | |||||||
| chr11:36280006 | T | A | 78 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.177+706A>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280006 | |||||||
| chr11:36280130 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.177+582A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280130 | |||||||
| chr11:36280133 | G | A | 1 | a0001c0006t0001g0140 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.177+579C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280133 | |||||||
| chr11:36280298 | G | A | 22 | a0001c0001t0001g0176 a0001c0001t0003g0002 a0001c0001t0003g0009 others(19): Show |
48 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.177+414C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280298 | |||||||
| chr11:36280503 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.177+209G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280503 | |||||||
| chr11:36280643 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.177+69A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280643 | |||||||
| chr11:36280860 | GA | G | 17 | a0001c0001t0004g0258 a0001c0001t0005g0038 a0001c0001t0005g0065 others(14): Show |
19 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.52-24delT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36280860 | |||||||
| chr11:36280971 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.52-134C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36280971 | |||||||
| chr11:36280978 | C | G | 1 | a0001c0001t0013g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52-141G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36280978 | |||||||
| chr11:36281107 | G | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.52-270C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281107 | |||||||
| chr11:36281239 | T | C | 17 | a0001c0001t0001g0119 a0001c0001t0005g0038 a0001c0001t0005g0065 others(14): Show |
19 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.52-402A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281239 | |||||||
| chr11:36281316 | A | G | 24 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(21): Show |
50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.52-479T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281316 | |||||||
| chr11:36281550 | T | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0083 |
9 | HG00673.hp2 HG02132.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-713A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281550 | |||||||
| chr11:36281719 | A | G | 1 | a0001c0001t0003g0175 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.52-882T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281719 | |||||||
| chr11:36281826 | C | G | 1 | a0001c0001t0002g0089 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.52-989G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281826 | |||||||
| chr11:36281907 | C | T | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-1070G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281907 | |||||||
| chr11:36281920 | T | C | 40 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0051 others(37): Show |
49 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.52-1083A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281920 | |||||||
| chr11:36281959 | C | A | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-1122G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281959 | |||||||
| chr11:36282152 | C | T | 1 | a0001c0001t0004g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.52-1315G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282152 | |||||||
| chr11:36282388 | A | G | 1 | a0001c0001t0001g0062 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.52-1551T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282388 | |||||||
| chr11:36282413 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.52-1576G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282413 | |||||||
| chr11:36282462 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-1625T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282462 | |||||||
| chr11:36282463 | AAACCATG others(25): Show |
A | 1 | a0001c0001t0005g0117 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.52-1658_52-1627del others(32): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282463 | |||||||
| chr11:36282513 | G | GA | 17 | a0001c0001t0003g0177 a0001c0001t0005g0038 a0001c0001t0005g0065 others(14): Show |
19 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.52-1677dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282513 | |||||||
| chr11:36282581 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52-1744C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282581 | |||||||
| chr11:36282701 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.52-1864T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282701 | |||||||
| chr11:36282731 | G | A | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-1894C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282731 | |||||||
| chr11:36282792 | G | T | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.52-1955C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282792 | |||||||
| chr11:36282793 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.52-1956C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282793 | |||||||
| chr11:36282795 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.52-1958T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282795 | |||||||
| chr11:36282796 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.52-1959T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282796 | |||||||
| chr11:36283101 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-2264T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283101 | |||||||
| chr11:36283190 | C | T | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-2353G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283190 | |||||||
| chr11:36283262 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.52-2425T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283262 | |||||||
| chr11:36283401 | G | A | 7 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | HG00741.hp1 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-2564C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283401 | |||||||
| chr11:36283482 | T | C | 1 | a0001c0001t0013g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52-2645A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283482 | |||||||
| chr11:36283604 | A | T | 1 | a0001c0001t0004g0272 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.52-2767T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283604 | |||||||
| chr11:36283674 | G | T | 24 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(21): Show |
50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.52-2837C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283674 | |||||||
| chr11:36283957 | T | G | 1 | a0001c0001t0017g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.52-3120A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283957 | |||||||
| chr11:36284104 | T | TCAA | 59 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0188 others(56): Show |
110 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.52-3270_52-3268dup others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | |||||||
| chr11:36284104 | T | TCAACAA | 23 | a0001c0001t0001g0176 a0001c0001t0002g0022 a0001c0001t0002g0032 others(20): Show |
31 | HG00438.hp2 HG00597.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.52-3273_52-3268dup others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | |||||||
| chr11:36284104 | TCAA | T | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.52-3270_52-3268del others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | |||||||
| chr11:36284104 | TCAACAA | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0106 a0001c0001t0001g0243 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.52-3273_52-3268del others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | |||||||
| chr11:36284104 | TCAACAAC others(5): Show |
T | 2 | a0001c0001t0003g0180 a0001c0001t0003g0182 |
2 | NA18964.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.52-3279_52-3268del others(12): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | |||||||
| chr11:36284104 | TCAACAAC others(8): Show |
T | 1 | a0001c0001t0001g0063 | 2 | HG01109.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.52-3282_52-3268del others(15): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | |||||||
| chr11:36284300 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.52-3463C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284300 | |||||||
| chr11:36284406 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52-3569C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284406 | |||||||
| chr11:36284652 | G | C | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-3815C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284652 | |||||||
| chr11:36284712 | T | C | 5 | a0001c0001t0002g0034 a0001c0001t0002g0076 a0001c0001t0002g0078 others(2): Show |
6 | HG00735.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-3875A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284712 | |||||||
| chr11:36284988 | A | G | 96 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
137 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.52-4151T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284988 | |||||||
| chr11:36285605 | G | A | 2 | a0001c0001t0005g0115 a0001c0001t0005g0118 |
2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.51+3757C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285605 | |||||||
| chr11:36285745 | A | G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+3617T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285745 | |||||||
| chr11:36285791 | C | T | 24 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(21): Show |
50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.51+3571G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285791 | |||||||
| chr11:36285793 | T | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.51+3569A>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285793 | |||||||
| chr11:36285797 | A | G | 98 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
139 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.51+3565T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285797 | |||||||
| chr11:36285806 | T | C | 15 | a0001c0001t0001g0119 a0001c0001t0005g0038 a0001c0001t0005g0065 others(12): Show |
17 | HG00438.hp2 HG00733.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.51+3556A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285806 | |||||||
| chr11:36285867 | G | C | 15 | a0001c0001t0001g0119 a0001c0001t0005g0038 a0001c0001t0005g0065 others(12): Show |
17 | HG00438.hp2 HG00733.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.51+3495C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285867 | |||||||
| chr11:36285972 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+3390T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285972 | |||||||
| chr11:36285973 | G | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+3389C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285973 | |||||||
| chr11:36286046 | CAAGGAAA others(139): Show |
C | 1 | a0001c0001t0001g0188 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+3170_51+3315del | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286046 | |||||||
| chr11:36286050 | G | A | 7 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | HG00741.hp1 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+3312C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286050 | |||||||
| chr11:36286395 | C | CAA | 73 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0051 others(70): Show |
128 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.51+2965_51+2966dup others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | |||||||
| chr11:36286395 | C | CAAA | 8 | a0001c0001t0001g0042 a0001c0001t0001g0201 a0001c0001t0002g0033 others(5): Show |
12 | HG01981.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.51+2964_51+2966dup others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | |||||||
| chr11:36286395 | C | CAAAA | 26 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(23): Show |
53 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.51+2963_51+2966dup others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | |||||||
| chr11:36286395 | C | CAAAAA | 5 | a0001c0001t0001g0024 a0001c0001t0001g0130 a0001c0001t0001g0138 others(2): Show |
7 | HG01070.hp2 HG01358.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2962_51+2966dup others(5): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | |||||||
| chr11:36286395 | CA | C | 13 | a0001c0001t0001g0119 a0001c0001t0005g0038 a0001c0001t0005g0065 others(10): Show |
15 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.51+2966delT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | |||||||
| chr11:36286408 | AAAAAAGA others(11): Show |
A | 17 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(14): Show |
22 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.51+2936_51+2953del others(18): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286408 | |||||||
| chr11:36286409 | AAAAAGAA others(10): Show |
A | 9 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(6): Show |
9 | HG00621.hp1 HG01928.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+2936_51+2952del others(17): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286409 | |||||||
| chr11:36286410 | A | AAAAAAAG others(4): Show |
1 | a0001c0001t0001g0197 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.51+2951_51+2952ins others(11): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286410 | |||||||
| chr11:36286410 | A | AAAAAAG | 6 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
6 | HG00280.hp1 HG01358.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+2951_51+2952ins others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286410 | |||||||
| chr11:36286410 | A | AAAG | 2 | a0001c0001t0001g0007 a0001c0001t0001g0127 |
7 | HG01261.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2951_51+2952ins others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286410 | |||||||
| chr11:36286410 | AAAAGAAA others(9): Show |
A | 68 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(65): Show |
94 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.51+2936_51+2951del others(16): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286410 | |||||||
| chr11:36286411 | AAAGAAAG others(8): Show |
A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0063 others(4): Show |
13 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2936_51+2950del others(15): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286411 | |||||||
| chr11:36286412 | AAGAAAG | A | 6 | a0001c0001t0001g0123 a0001c0001t0006g0098 a0001c0001t0006g0099 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+2944_51+2949del others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286412 | |||||||
| chr11:36286412 | AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0002g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.51+2940_51+2949del others(10): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286412 | |||||||
| chr11:36286414 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0134 |
4 | NA18954.hp2 NA18969.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2948C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286414 | |||||||
| chr11:36286427 | AAAG | A | 22 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(19): Show |
47 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.51+2932_51+2934del others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286427 | |||||||
| chr11:36286435 | AAAAG | A | 22 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(19): Show |
47 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.51+2923_51+2926del others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286435 | |||||||
| chr11:36286438 | A | G | 2 | a0002c0002t0006g0071 a0002c0002t0006g0072 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.51+2924T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286438 | |||||||
| chr11:36286439 | G | A | 2 | a0002c0002t0006g0071 a0002c0002t0006g0072 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.51+2923C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286439 | |||||||
| chr11:36286439 | G | GA | 129 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.51+2922dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286439 | |||||||
| chr11:36286443 | A | G | 2 | a0002c0002t0006g0071 a0002c0002t0006g0072 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.51+2919T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286443 | |||||||
| chr11:36286463 | G | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0202 others(2): Show |
7 | HG02257.hp1 HG02572.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+2899C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286463 | |||||||
| chr11:36286506 | T | C | 1 | a0001c0001t0002g0037 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.51+2856A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286506 | |||||||
| chr11:36286597 | A | AAAAC | 4 | a0001c0001t0001g0119 a0001c0001t0003g0184 a0001c0001t0003g0185 others(1): Show |
4 | HG01243.hp2 HG02004.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2761_51+2764dup others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286597 | |||||||
| chr11:36286623 | A | C | 1 | a0001c0001t0002g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.51+2739T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286623 | |||||||
| chr11:36286643 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.51+2719C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286643 | |||||||
| chr11:36286705 | T | C | 24 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0003g0002 others(21): Show |
50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.51+2657A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286705 | |||||||
| chr11:36286743 | A | C | 1 | a0001c0001t0002g0087 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.51+2619T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286743 | |||||||
| chr11:36286755 | T | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.51+2607A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286755 | |||||||
| chr11:36286891 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | NA18940.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.51+2471C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286891 | |||||||
| chr11:36286903 | A | C | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.51+2459T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286903 | |||||||
| chr11:36286916 | C | G | 1 | a0001c0001t0003g0181 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.51+2446G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286916 | |||||||
| chr11:36286940 | T | C | 1 | a0001c0001t0001g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.51+2422A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286940 | |||||||
| chr11:36286947 | ACTGTCAA others(57): Show |
A | 1 | a0001c0001t0005g0109 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.51+2351_51+2414del others(64): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286947 | |||||||
| chr11:36287046 | A | ATATGTAT others(153): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0013g0148 |
3 | HG01081.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(160): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(217): Show |
4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG01361.hp2 HG02074.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(224): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(249): Show |
5 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0070 others(2): Show |
13 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(256): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(281): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0041 others(4): Show |
17 | HG01167.hp1 HG01255.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(288): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(313): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0042 others(5): Show |
18 | HG00140.hp1 HG00140.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(345): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0066 others(5): Show |
12 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(377): Show |
10 | a0001c0001t0001g0039 a0001c0001t0001g0131 a0001c0001t0001g0132 others(7): Show |
15 | HG00621.hp2 HG01123.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(384): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(409): Show |
4 | a0001c0001t0003g0002 a0001c0001t0003g0047 a0001c0001t0003g0179 others(1): Show |
18 | HG00609.hp1 HG01993.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(416): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(441): Show |
3 | a0001c0001t0001g0130 a0001c0001t0003g0009 a0001c0001t0003g0278 |
7 | HG00408.hp2 HG01978.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(448): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1579): Show |
1 | a0001c0001t0001g0188 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1586): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(505): Show |
1 | a0001c0001t0003g0046 | 2 | NA18986.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(537): Show |
1 | a0001c0001t0003g0178 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(544): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(789): Show |
1 | a0001c0001t0001g0213 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(796): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(569): Show |
1 | a0001c0001t0001g0056 | 2 | HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(576): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(601): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG01192.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(608): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(633): Show |
2 | a0001c0001t0001g0027 a0001c0001t0003g0177 |
4 | HG02165.hp2 HG03130.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(640): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(665): Show |
1 | a0001c0001t0001g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(672): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(697): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0209 a0001c0001t0016g0208 |
4 | HG02886.hp2 NA18906.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(704): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(729): Show |
3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG03540.hp1 HG03710.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(736): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(761): Show |
3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0153 |
5 | HG01099.hp2 HG01361.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(768): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(793): Show |
2 | a0001c0001t0001g0052 a0001c0001t0001g0152 |
3 | HG00733.hp1 HG01256.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(800): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(825): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0151 a0001c0001t0001g0203 others(1): Show |
5 | HG01255.hp2 HG01952.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(832): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(857): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01981.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(864): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(921): Show |
1 | a0001c0001t0001g0200 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(928): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(985): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03209.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(992): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1017): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0197 |
3 | HG01081.hp1 HG02300.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(1024): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1049): Show |
1 | a0001c0001t0001g0150 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1056): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1081): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0196 |
2 | HG02630.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(1088): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1145): Show |
3 | a0001c0001t0001g0149 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG00609.hp2 HG04199.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(1152): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1177): Show |
2 | a0001c0001t0001g0192 a0001c0005t0001g0193 |
2 | HG03942.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(1184): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1273): Show |
1 | a0001c0001t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1280): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1305): Show |
1 | a0001c0001t0001g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1312): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1849): Show |
1 | a0001c0001t0001g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1856): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(313): Show |
1 | a0001c0001t0001g0129 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(313): Show |
1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(441): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0127 |
7 | HG01261.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(448): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1145): Show |
1 | a0001c0001t0001g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1152): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1209): Show |
1 | a0001c0001t0001g0275 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1216): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1273): Show |
1 | a0001c0001t0001g0274 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1280): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287046 | A | ATATGTAT others(1465): Show |
1 | a0001c0001t0005g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1472): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | |||||||
| chr11:36287054 | A | ACTACATA others(697): Show |
1 | a0001c0001t0005g0117 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(704): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(761): Show |
1 | a0001c0001t0005g0065 | 2 | HG00438.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.51+2307_51+2308ins others(768): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(1145): Show |
1 | a0001c0001t0005g0038 | 2 | HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.51+2307_51+2308ins others(1152): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(1177): Show |
1 | a0001c0001t0005g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1184): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(1273): Show |
1 | a0001c0001t0005g0109 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1280): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(1305): Show |
1 | a0001c0001t0005g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1312): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(1433): Show |
1 | a0001c0001t0005g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1440): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(1817): Show |
1 | a0001c0001t0005g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1824): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(1945): Show |
1 | a0001c0001t0005g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1952): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(2233): Show |
1 | a0001c0001t0005g0114 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(2240): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | ACTACATA others(2841): Show |
1 | a0001c0001t0005g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(2848): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287054 | A | G | 1 | a0001c0001t0005g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.51+2308T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | |||||||
| chr11:36287056 | T | TACATACT others(505): Show |
3 | a0001c0001t0007g0043 a0001c0001t0007g0154 a0001c0004t0007g0155 |
4 | HG02895.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2305_51+2306ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287056 | |||||||
| chr11:36287056 | T | TACATACT others(537): Show |
1 | a0001c0001t0007g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.51+2305_51+2306ins others(544): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287056 | |||||||
| chr11:36287061 | A | ACTATGTA others(313): Show |
1 | a0002c0002t0006g0072 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(345): Show |
2 | a0001c0001t0002g0082 a0002c0002t0006g0071 |
2 | HG02056.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.51+2300_51+2301ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(755): Show |
1 | a0001c0001t0002g0075 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(762): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(726): Show |
1 | a0001c0001t0002g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(733): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(790): Show |
1 | a0001c0001t0002g0081 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(797): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(726): Show |
1 | a0001c0001t0002g0086 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(733): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(822): Show |
3 | a0001c0001t0002g0034 a0001c0001t0002g0079 a0001c0001t0002g0080 |
4 | HG01256.hp2 HG01258.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2300_51+2301ins others(829): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(854): Show |
1 | a0001c0001t0002g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(758): Show |
1 | a0001c0001t0002g0085 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(765): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(854): Show |
1 | a0001c0001t0002g0078 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(886): Show |
1 | a0001c0001t0002g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(893): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(505): Show |
1 | a0001c0001t0006g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(854): Show |
1 | a0001c0001t0002g0083 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(537): Show |
2 | a0001c0001t0006g0100 a0001c0001t0006g0101 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.51+2300_51+2301ins others(544): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(569): Show |
1 | a0001c0001t0006g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(576): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287061 | A | ACTATGTA others(537): Show |
1 | a0001c0001t0006g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(544): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | |||||||
| chr11:36287069 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2293A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287069 | |||||||
| chr11:36287073 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2289C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287073 | |||||||
| chr11:36287074 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2288G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287074 | |||||||
| chr11:36287075 | G | A | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.51+2287C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | |||||||
| chr11:36287075 | G | ATAGCATG others(217): Show |
1 | a0001c0001t0004g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.51+2287_51+2288ins others(224): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | |||||||
| chr11:36287075 | G | ATAGCATG others(281): Show |
1 | a0001c0001t0004g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.51+2287_51+2288ins others(288): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | |||||||
| chr11:36287075 | G | ATAGCATG others(313): Show |
5 | a0001c0001t0004g0159 a0001c0001t0004g0168 a0001c0001t0004g0169 others(2): Show |
5 | HG00621.hp1 NA18952.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+2287_51+2288ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | |||||||
| chr11:36287075 | G | ATAGCATG others(345): Show |
1 | a0001c0001t0004g0158 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.51+2287_51+2288ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | |||||||
| chr11:36287075 | G | ATAGCATG others(377): Show |
2 | a0001c0001t0004g0045 a0001c0001t0004g0157 |
3 | HG01981.hp2 HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.51+2287_51+2288ins others(384): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | |||||||
| chr11:36287075 | G | ATAGCATG others(409): Show |
1 | a0001c0001t0004g0015 | 4 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2287_51+2288ins others(416): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | |||||||
| chr11:36287075 | G | ATAGCATG others(473): Show |
1 | a0001c0001t0004g0167 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.51+2287_51+2288ins others(480): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | |||||||
| chr11:36287076 | T | TAGCATGT others(313): Show |
1 | a0001c0001t0004g0164 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.51+2285_51+2286ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287076 | |||||||
| chr11:36287076 | T | TAGCATGT others(313): Show |
2 | a0001c0001t0004g0044 a0001c0001t0004g0162 |
3 | NA18945.hp2 NA18995.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.51+2285_51+2286ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287076 | |||||||
| chr11:36287076 | T | TAGCATGT others(345): Show |
1 | a0001c0001t0004g0163 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.51+2285_51+2286ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287076 | |||||||
| chr11:36287079 | T | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(17): Show |
25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2283A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287079 | |||||||
| chr11:36287086 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2276T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287086 | |||||||
| chr11:36287088 | T | C | 4 | a0001c0001t0007g0043 a0001c0001t0007g0154 a0001c0001t0007g0156 others(1): Show |
5 | HG02451.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2274A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287088 | |||||||
| chr11:36287088 | T | TACAATGT others(781): Show |
1 | a0001c0001t0001g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.51+2273_51+2274ins others(788): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287088 | |||||||
| chr11:36287088 | T | TACAATGT others(1009): Show |
1 | a0001c0001t0001g0251 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.51+2273_51+2274ins others(1016): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287088 | |||||||
| chr11:36287088 | T | TACAATGT others(909): Show |
1 | a0001c0001t0001g0239 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.51+2273_51+2274ins others(916): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287088 | |||||||
| chr11:36287093 | A | ACTATGTA others(249): Show |
1 | a0001c0001t0002g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(256): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(313): Show |
1 | a0002c0002t0006g0073 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(726): Show |
1 | a0001c0001t0002g0001 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(733): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(819): Show |
1 | a0001c0001t0002g0001 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(826): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(851): Show |
1 | a0001c0001t0002g0035 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(858): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(630): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0087 |
2 | NA18984.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(637): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(758): Show |
1 | a0001c0001t0002g0001 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(765): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(790): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0036 a0001c0001t0002g0089 |
4 | HG00597.hp2 NA18966.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(797): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(950): Show |
1 | a0001c0001t0002g0095 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(957): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(787): Show |
1 | a0001c0001t0002g0001 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(794): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(758): Show |
1 | a0001c0001t0002g0001 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(765): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(822): Show |
1 | a0001c0001t0002g0001 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(829): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(854): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0035 |
5 | HG02027.hp1 HG02135.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(982): Show |
1 | a0001c0001t0002g0094 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(989): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(441): Show |
1 | a0001c0001t0002g0003 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(448): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(851): Show |
1 | a0001c0001t0002g0001 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(858): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(947): Show |
1 | a0001c0001t0002g0012 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(954): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(758): Show |
2 | a0001c0001t0002g0003 a0001c0001t0002g0074 |
3 | HG03017.hp2 NA18978.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(765): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(790): Show |
1 | a0001c0001t0002g0003 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(797): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(854): Show |
5 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(2): Show |
6 | HG00438.hp1 HG01192.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(886): Show |
1 | a0001c0001t0002g0003 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(893): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(982): Show |
1 | a0001c0001t0008g0021 | 2 | NA18939.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(989): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(1078): Show |
1 | a0001c0001t0002g0022 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1085): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(851): Show |
1 | a0001c0001t0002g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(858): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(915): Show |
1 | a0001c0001t0002g0012 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(922): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(1043): Show |
1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1050): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(790): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0020 |
3 | NA18943.hp1 NA18983.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(797): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(854): Show |
1 | a0001c0001t0002g0003 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(886): Show |
1 | a0001c0001t0002g0001 | 8 | HG00544.hp2 NA18946.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(893): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(1014): Show |
1 | a0001c0001t0008g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1021): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(505): Show |
1 | a0001c0001t0002g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(883): Show |
1 | a0001c0001t0002g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(890): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(822): Show |
1 | a0001c0001t0002g0022 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(829): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(761): Show |
1 | a0001c0001t0002g0013 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(768): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(857): Show |
2 | a0001c0001t0002g0037 a0001c0001t0002g0090 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(864): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(889): Show |
1 | a0001c0001t0002g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(896): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(921): Show |
2 | a0001c0001t0002g0091 a0001c0001t0002g0104 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(928): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(985): Show |
1 | a0001c0001t0002g0096 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(992): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(1017): Show |
1 | a0001c0001t0002g0001 | 2 | NA19070.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(1024): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(1081): Show |
1 | a0001c0001t0002g0001 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1088): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(1113): Show |
1 | a0001c0001t0002g0001 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1120): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | ACTATGTA others(1145): Show |
1 | a0001c0001t0002g0033 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(1152): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287093 | A | G | 20 | a0001c0001t0002g0034 a0001c0001t0002g0075 a0001c0001t0002g0076 others(17): Show |
21 | HG00280.hp1 HG01256.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.51+2269T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | |||||||
| chr11:36287094 | C | CTATGTAC others(873): Show |
1 | a0001c0001t0002g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.51+2267_51+2268ins others(880): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287094 | |||||||
| chr11:36287101 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2261A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287101 | |||||||
| chr11:36287105 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2257C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287105 | |||||||
| chr11:36287106 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2256G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287106 | |||||||
| chr11:36287107 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+2255C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287107 | |||||||
| chr11:36287108 | T | TAGCATGT others(281): Show |
1 | a0001c0001t0004g0166 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.51+2253_51+2254ins others(288): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287108 | |||||||
| chr11:36287108 | T | TAGCATGT others(313): Show |
2 | a0001c0001t0004g0165 a0001c0001t0004g0171 |
2 | HG01934.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.51+2253_51+2254ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287108 | |||||||
| chr11:36287108 | T | TAGCATGT others(345): Show |
1 | a0001c0001t0004g0172 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.51+2253_51+2254ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287108 | |||||||
| chr11:36287111 | T | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(17): Show |
25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2251A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287111 | |||||||
| chr11:36287118 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2244T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287118 | |||||||
| chr11:36287120 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0239 a0001c0001t0001g0251 others(4): Show |
8 | HG00280.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+2242A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(754): Show |
1 | a0001c0001t0001g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(761): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(789): Show |
1 | a0001c0001t0002g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(796): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(853): Show |
1 | a0001c0001t0001g0236 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(860): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(913): Show |
1 | a0001c0001t0001g0233 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(920): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(945): Show |
1 | a0001c0001t0001g0240 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(952): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1041): Show |
1 | a0001c0001t0001g0248 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1048): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(689): Show |
1 | a0001c0001t0004g0258 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(696): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(401): Show |
1 | a0001c0001t0001g0018 | 4 | NA18747.hp2 NA18969.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(408): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(561): Show |
1 | a0001c0001t0001g0219 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(568): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(657): Show |
2 | a0001c0001t0001g0265 a0001c0001t0004g0028 |
4 | HG00642.hp2 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(664): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(689): Show |
1 | a0001c0001t0004g0016 | 4 | HG02148.hp2 HG02273.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(696): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(721): Show |
1 | a0001c0001t0004g0272 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(728): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(753): Show |
1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(760): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(785): Show |
1 | a0001c0001t0001g0057 | 2 | HG03492.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(792): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(817): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0229 |
3 | HG01099.hp1 HG01106.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(824): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(881): Show |
2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | NA18945.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(888): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(913): Show |
1 | a0001c0001t0001g0010 | 5 | HG00558.hp1 HG01943.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(920): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(945): Show |
2 | a0001c0001t0001g0060 a0001c0001t0001g0243 |
3 | HG01433.hp2 HG01515.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(952): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(977): Show |
3 | a0001c0001t0001g0008 a0001c0001t0001g0246 a0001c0001t0001g0247 |
8 | HG02647.hp2 HG03017.hp1 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(984): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1009): Show |
2 | a0001c0001t0001g0250 a0001c0001t0010g0249 |
2 | HG02970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1016): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1041): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0061 a0001c0001t0001g0062 |
8 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1048): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1105): Show |
1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1112): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1137): Show |
1 | a0001c0001t0001g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1144): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1169): Show |
1 | a0001c0001t0001g0063 | 2 | HG01109.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1176): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1457): Show |
1 | a0001c0001t0001g0064 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1464): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1489): Show |
1 | a0001c0001t0001g0255 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1496): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(2033): Show |
1 | a0001c0001t0001g0256 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(2040): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(909): Show |
1 | a0001c0001t0001g0030 | 3 | HG00544.hp1 NA18952.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(916): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(941): Show |
1 | a0001c0001t0001g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(948): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(397): Show |
1 | a0001c0001t0001g0263 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(404): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(685): Show |
1 | a0001c0001t0001g0220 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(692): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(717): Show |
1 | a0001c0001t0001g0221 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(724): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(749): Show |
1 | a0001c0001t0015g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(756): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(845): Show |
1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(852): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(877): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0266 |
2 | HG01928.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(884): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(941): Show |
2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG01952.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(948): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(973): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0273 |
3 | HG02040.hp1 HG02056.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(980): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(937): Show |
1 | a0001c0001t0001g0029 | 3 | NA18943.hp2 NA18953.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(944): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(965): Show |
1 | a0001c0001t0001g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(972): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(753): Show |
1 | a0001c0001t0001g0226 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(760): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(849): Show |
1 | a0001c0001t0001g0215 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(856): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(881): Show |
1 | a0001c0001t0001g0241 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(888): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(913): Show |
1 | a0001c0001t0001g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(920): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1009): Show |
1 | a0001c0001t0001g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1016): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(1041): Show |
2 | a0001c0001t0001g0216 a0001c0001t0001g0253 |
2 | HG02717.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1048): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287120 | T | TACAATGT others(397): Show |
1 | a0001c0001t0001g0264 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(404): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | |||||||
| chr11:36287123 | ATACT | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0119 a0001c0001t0001g0217 others(7): Show |
14 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.51+2235_51+2238del others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287123 | |||||||
| chr11:36287125 | A | ACTATGTA others(761): Show |
1 | a0001c0001t0002g0020 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.51+2236_51+2237ins others(768): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287125 | |||||||
| chr11:36287125 | A | ACTATGTA others(857): Show |
1 | a0001c0001t0002g0001 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.51+2236_51+2237ins others(864): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287125 | |||||||
| chr11:36287125 | A | ACTATGTA others(953): Show |
2 | a0001c0001t0002g0020 a0001c0001t0002g0103 |
2 | HG01891.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.51+2236_51+2237ins others(960): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287125 | |||||||
| chr11:36287125 | A | G | 47 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(44): Show |
95 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.51+2237T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287125 | |||||||
| chr11:36287133 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2229A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287133 | |||||||
| chr11:36287137 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2225C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287137 | |||||||
| chr11:36287138 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2224G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287138 | |||||||
| chr11:36287139 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+2223C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287139 | |||||||
| chr11:36287143 | T | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(17): Show |
25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2219A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287143 | |||||||
| chr11:36287150 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2212T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287150 | |||||||
| chr11:36287152 | T | C | 67 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0017 others(64): Show |
100 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.51+2210A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287152 | |||||||
| chr11:36287152 | T | TACAATGT others(849): Show |
1 | a0001c0001t0001g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.51+2209_51+2210ins others(856): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287152 | |||||||
| chr11:36287152 | T | TACAATGT others(977): Show |
1 | a0001c0001t0001g0242 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.51+2209_51+2210ins others(984): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287152 | |||||||
| chr11:36287152 | T | TACAATGT others(1009): Show |
1 | a0001c0001t0010g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.51+2209_51+2210ins others(1016): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287152 | |||||||
| chr11:36287157 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2205T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287157 | |||||||
| chr11:36287165 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2197A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287165 | |||||||
| chr11:36287169 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2193C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287169 | |||||||
| chr11:36287170 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2192G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287170 | |||||||
| chr11:36287171 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+2191C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287171 | |||||||
| chr11:36287175 | T | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(17): Show |
25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2187A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287175 | |||||||
| chr11:36287182 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2180T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287182 | |||||||
| chr11:36287184 | T | C | 71 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0017 others(68): Show |
104 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.51+2178A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287184 | |||||||
| chr11:36287184 | T | TACTATGT others(941): Show |
1 | a0001c0001t0001g0218 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.51+2177_51+2178ins others(948): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287184 | |||||||
| chr11:36287185 | A | C | 2 | a0003c0003t0005g0067 a0003c0003t0005g0068 |
2 | HG01109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.51+2177T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287185 | |||||||
| chr11:36287189 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2173T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287189 | |||||||
| chr11:36287197 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2165A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287197 | |||||||
| chr11:36287201 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2161C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287201 | |||||||
| chr11:36287202 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2160G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287202 | |||||||
| chr11:36287203 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+2159C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287203 | |||||||
| chr11:36287207 | T | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(17): Show |
25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2155A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287207 | |||||||
| chr11:36287214 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2148T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287214 | |||||||
| chr11:36287216 | T | C | 70 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0017 others(67): Show |
103 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.51+2146A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(405): Show |
1 | a0001c0001t0001g0011 | 5 | NA18949.hp1 NA18955.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2145_51+2146ins others(412): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(437): Show |
1 | a0001c0001t0001g0269 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(444): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(469): Show |
1 | a0001c0001t0001g0259 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(476): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(565): Show |
1 | a0001c0001t0001g0260 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(572): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(789): Show |
1 | a0001c0001t0001g0270 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(796): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(853): Show |
1 | a0001c0001t0001g0271 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(860): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(949): Show |
1 | a0001c0001t0001g0119 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(956): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(946): Show |
1 | a0001c0001t0001g0217 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(953): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(401): Show |
1 | a0001c0001t0001g0267 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(408): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(433): Show |
1 | a0001c0001t0001g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(440): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287216 | T | TACTATGT others(909): Show |
1 | a0001c0001t0001g0262 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(916): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | |||||||
| chr11:36287217 | A | C | 2 | a0003c0003t0005g0067 a0003c0003t0005g0068 |
2 | HG01109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.51+2145T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287217 | |||||||
| chr11:36287221 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2141T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287221 | |||||||
| chr11:36287229 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2133A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287229 | |||||||
| chr11:36287233 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2129C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287233 | |||||||
| chr11:36287234 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2128G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287234 | |||||||
| chr11:36287235 | G | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.51+2127C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287235 | |||||||
| chr11:36287239 | T | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0001c0001t0004g0045 others(17): Show |
25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2123A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287239 | |||||||
| chr11:36287246 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2116T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287246 | |||||||
| chr11:36287248 | T | C | 81 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.51+2114A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287248 | |||||||
| chr11:36287248 | T | TACTATGT others(941): Show |
1 | a0001c0001t0001g0261 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.51+2113_51+2114ins others(948): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287248 | |||||||
| chr11:36287249 | A | C | 2 | a0003c0003t0005g0067 a0003c0003t0005g0068 |
2 | HG01109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.51+2113T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287249 | |||||||
| chr11:36287253 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2109T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287253 | |||||||
| chr11:36287261 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2101A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287261 | |||||||
| chr11:36287265 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2097C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287265 | |||||||
| chr11:36287266 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2096G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287266 | |||||||
| chr11:36287267 | G | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.51+2095C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287267 | |||||||
| chr11:36287271 | T | C | 18 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0158 others(15): Show |
20 | HG00558.hp2 HG00621.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.51+2091A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287271 | |||||||
| chr11:36287278 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2084T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287278 | |||||||
| chr11:36287279 | C | CTACATAC others(505): Show |
1 | a0001c0001t0017g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.51+2082_51+2083ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287279 | |||||||
| chr11:36287280 | T | C | 82 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.51+2082A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287280 | |||||||
| chr11:36287281 | A | C | 2 | a0003c0003t0005g0067 a0003c0003t0005g0068 |
2 | HG01109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.51+2081T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287281 | |||||||
| chr11:36287285 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2077T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287285 | |||||||
| chr11:36287293 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2069A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287293 | |||||||
| chr11:36287297 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2065C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287297 | |||||||
| chr11:36287298 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2064G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287298 | |||||||
| chr11:36287299 | G | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.51+2063C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287299 | |||||||
| chr11:36287303 | T | C | 8 | a0001c0001t0004g0045 a0001c0001t0004g0167 a0001c0001t0004g0168 others(5): Show |
9 | HG01934.hp2 HG01981.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+2059A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287303 | |||||||
| chr11:36287310 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2052T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287310 | |||||||
| chr11:36287312 | T | C | 82 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.51+2050A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287312 | |||||||
| chr11:36287313 | A | C | 1 | a0003c0003t0005g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51+2049T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287313 | |||||||
| chr11:36287313 | A | CCATACTA others(1945): Show |
1 | a0003c0003t0005g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.51+2049_51+2050ins others(1952): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287313 | |||||||
| chr11:36287317 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2045T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287317 | |||||||
| chr11:36287325 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2037A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287325 | |||||||
| chr11:36287329 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2033C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287329 | |||||||
| chr11:36287330 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2032G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287330 | |||||||
| chr11:36287331 | G | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.51+2031C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287331 | |||||||
| chr11:36287335 | T | C | 1 | a0001c0001t0004g0173 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.51+2027A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287335 | |||||||
| chr11:36287342 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2020T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287342 | |||||||
| chr11:36287344 | T | C | 82 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.51+2018A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287344 | |||||||
| chr11:36287345 | A | C | 1 | a0003c0003t0005g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51+2017T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287345 | |||||||
| chr11:36287349 | A | G | 47 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(44): Show |
98 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.51+2013T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287349 | |||||||
| chr11:36287357 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2005A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287357 | |||||||
| chr11:36287361 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2001C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287361 | |||||||
| chr11:36287362 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+2000G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287362 | |||||||
| chr11:36287363 | G | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.51+1999C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287363 | |||||||
| chr11:36287363 | G | GTAGTATG others(857): Show |
1 | a0001c0001t0001g0123 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.51+1998_51+1999ins others(864): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287363 | |||||||
| chr11:36287367 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.51+1995A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287367 | |||||||
| chr11:36287374 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+1988T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287374 | |||||||
| chr11:36287376 | T | C | 82 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.51+1986A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287376 | |||||||
| chr11:36287377 | A | C | 1 | a0003c0003t0005g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51+1985T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287377 | |||||||
| chr11:36287381 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+1981T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287381 | |||||||
| chr11:36287389 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+1973A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287389 | |||||||
| chr11:36287393 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+1969C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287393 | |||||||
| chr11:36287394 | C | T | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
intron_variant | MODIFIER | c.51+1968G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287394 | |||||||
| chr11:36287395 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+1967C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287395 | |||||||
| chr11:36287406 | A | G | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+1956T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287406 | |||||||
| chr11:36287408 | T | C | 80 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(77): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.51+1954A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287408 | |||||||
| chr11:36287409 | A | CCATACTA others(1497): Show |
1 | a0003c0003t0005g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51+1953_51+1954ins others(1504): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287409 | |||||||
| chr11:36287413 | A | G | 6 | a0001c0001t0002g0012 a0001c0001t0002g0032 a0001c0001t0002g0033 others(3): Show |
11 | HG01891.hp2 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.51+1949T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287413 | |||||||
| chr11:36287421 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.51+1941A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287421 | |||||||
| chr11:36287425 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.51+1937C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287425 | |||||||
| chr11:36287426 | T | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0274 a0001c0001t0001g0275 others(1): Show |
4 | HG01243.hp1 HG01261.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+1936A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287426 | |||||||
| chr11:36287427 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+1935C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287427 | |||||||
| chr11:36287431 | T | C | 47 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(44): Show |
98 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.51+1931A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287431 | |||||||
| chr11:36287438 | A | G | 3 | a0001c0001t0005g0112 a0001c0001t0005g0118 a0001c0001t0012g0111 |
3 | HG02809.hp2 HG03041.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.51+1924T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287438 | |||||||
| chr11:36287440 | T | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0263 others(8): Show |
18 | HG00323.hp2 HG00642.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.51+1922A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287440 | T | TACATACT others(343): Show |
1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(350): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287440 | T | TACATACT others(375): Show |
1 | a0001c0001t0003g0026 | 3 | HG02559.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.51+1921_51+1922ins others(382): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287440 | T | TACATACT others(1340): Show |
1 | a0001c0001t0001g0126 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(1347): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287440 | T | TACATACT others(1372): Show |
1 | a0001c0001t0001g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(1379): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287440 | T | TACATACT others(2716): Show |
1 | a0001c0001t0001g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(2723): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287440 | T | TACATACT others(2391): Show |
1 | a0001c0001t0001g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(2398): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287440 | T | TACATACT others(1239): Show |
1 | a0001c0001t0005g0118 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(1246): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287440 | T | TACATACT others(2231): Show |
1 | a0001c0001t0012g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(2238): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | |||||||
| chr11:36287441 | C | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.51+1921G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287441 | |||||||
| chr11:36287442 | T | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.51+1920A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287442 | |||||||
| chr11:36287442 | T | TAC | 4 | a0001c0001t0001g0176 a0001c0001t0003g0026 a0001c0001t0005g0118 others(1): Show |
6 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+1919_51+1920ins others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287442 | |||||||
| chr11:36287443 | A | ACG | 4 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+1918_51+1919ins others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287443 | |||||||
| chr11:36287443 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.51+1919T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287443 | |||||||
| chr11:36287618 | A | T | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+1744T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287618 | |||||||
| chr11:36287667 | C | T | 3 | a0002c0002t0006g0071 a0002c0002t0006g0072 a0002c0002t0006g0073 |
3 | HG02615.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.51+1695G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287667 | |||||||
| chr11:36287744 | G | A | 16 | a0001c0001t0005g0038 a0001c0001t0005g0065 a0001c0001t0005g0107 others(13): Show |
18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+1618C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287744 | |||||||
| chr11:36287913 | T | C | 19 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0019 others(16): Show |
43 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.51+1449A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287913 | |||||||
| chr11:36288083 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.51+1279T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288083 | |||||||
| chr11:36288178 | A | G | 276 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
intron_variant | MODIFIER | c.51+1184T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288178 | |||||||
| chr11:36288194 | T | G | 1 | a0001c0001t0001g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.51+1168A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288194 | |||||||
| chr11:36288195 | G | A | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.51+1167C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288195 | |||||||
| chr11:36288356 | G | GT | 11 | a0001c0001t0001g0147 a0001c0001t0002g0097 a0001c0001t0002g0103 others(8): Show |
11 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.51+1005dupA | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288356 | |||||||
| chr11:36288359 | T | TA | 37 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0051 others(34): Show |
46 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.51+1002dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288359 | |||||||
| chr11:36288359 | T | TTA | 23 | a0001c0001t0001g0176 a0001c0001t0002g0037 a0001c0001t0003g0002 others(20): Show |
50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.51+1002_51+1003ins others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288359 | |||||||
| chr11:36288360 | A | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.51+1002T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288360 | |||||||
| chr11:36288361 | A | T | 8 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0005g0038 others(5): Show |
9 | HG02735.hp1 HG02738.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+1001T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288361 | |||||||
| chr11:36288374 | AG | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0042 others(28): Show |
35 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.51+987delC | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288374 | |||||||
| chr11:36288375 | G | A | 252 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(249): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.51+987C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288375 | |||||||
| chr11:36288379 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.51+983C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288379 | |||||||
| chr11:36288539 | A | C | 65 | a0001c0001t0001g0119 a0001c0001t0002g0001 a0001c0001t0002g0003 others(62): Show |
118 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.51+823T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288539 | |||||||
| chr11:36288694 | G | C | 77 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.51+668C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288694 | |||||||
| chr11:36288726 | G | C | 1 | a0001c0001t0005g0065 | 2 | HG00438.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.51+636C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288726 | |||||||
| chr11:36288733 | G | GA | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.51+628dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288733 | |||||||
| chr11:36288949 | T | C | 1 | a0001c0001t0001g0066 | 2 | NA18975.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.51+413A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288949 | |||||||
| chr11:36288951 | G | A | 1 | a0001c0001t0017g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.51+411C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288951 | |||||||
| chr11:36288983 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.51+379G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288983 | |||||||
| chr11:36289127 | C | T | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0012 others(45): Show |
99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+235G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36289127 | |||||||
| chr11:36289307 | C | A | 3 | a0001c0001t0003g0019 a0001c0001t0003g0278 a0001c0001t0003g0279 |
6 | HG00621.hp2 NA18942.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+55G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36289307 | |||||||
| chr11:36289347 | A | AC | 3 | a0001c0001t0001g0031 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG01123.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+14dupG | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36289347 |