Search by Gene
| Item | Value |
|---|---|
| geneid | 28971 |
| ensemblid | ENSG00000087884.16 |
| hgncid | 30205 |
| symbol | AAMDC |
| name | adipogenesis associated Mth938 domain containing |
| refseq_nuc | NM_024684.4 |
| refseq_prot | NP_078960.1 |
| ensembl_nuc | ENST00000393427.7 |
| ensembl_prot | ENSP00000377078.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 77821144 |
| end | 77872352 |
| strand | + |
| ver | v1.2 |
| region | chr11:77821144-77872352 |
| region5000 | chr11:77816144-77877352 |
| regionname0 | AAMDC_chr11_77821144_77872352 |
| regionname5000 | AAMDC_chr11_77816144_77877352 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 122 | 312 | 73 | 53 | 135 | 15 | 34 | AAMDC_chr11_77816144_77877352 | AAMDC | MTSPE others(117): Show |
chr11 | 77816144 | 77877352 |
| a0002 | 0/0 | 122 | 69 | 13 | 9 | 46 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | MTSPE others(117): Show |
chr11 | 77816144 | 77877352 |
| a0003 | 0/0 | 122 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | MTSPE others(117): Show |
chr11 | 77816144 | 77877352 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 366 | 215 | 34 | 35 | 114 | 11 | 19 | AAMDC_chr11_77816144_77877352 | AAMDC | ATGAC others(361): Show |
chr11 | 77816144 | 77877352 | ||
| a0001c0002 | 0/0 | 366 | 97 | 39 | 18 | 21 | 4 | 15 | AAMDC_chr11_77816144_77877352 | AAMDC | ATGAC others(361): Show |
chr11 | 77816144 | 77877352 | ||
| a0002c0003 | 0/0 | 366 | 68 | 13 | 9 | 45 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | ATGAC others(361): Show |
chr11 | 77816144 | 77877352 | ||
| a0002c0004 | 0/0 | 366 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | ATGAC others(361): Show |
chr11 | 77816144 | 77877352 | ||
| a0003c0005 | 0/0 | 366 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | ATGAC others(361): Show |
chr11 | 77816144 | 77877352 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 522 | 215 | 34 | 35 | 114 | 11 | 19 | AAMDC_chr11_77816144_77877352 | AAMDC | AGTTG others(517): Show |
chr11 | 77816144 | 77877352 |
| a0001c0002t0001 | 0/0 | 522 | 20 | 17 | 3 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | AGTTG others(517): Show |
chr11 | 77816144 | 77877352 |
| a0001c0002t0002 | 0/0 | 522 | 77 | 22 | 15 | 21 | 4 | 15 | AAMDC_chr11_77816144_77877352 | AAMDC | AGTTG others(517): Show |
chr11 | 77816144 | 77877352 |
| a0002c0003t0001 | 0/0 | 522 | 68 | 13 | 9 | 45 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | AGTTG others(517): Show |
chr11 | 77816144 | 77877352 |
| a0002c0004t0001 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | AGTTG others(517): Show |
chr11 | 77816144 | 77877352 |
| a0003c0005t0001 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | AGTTG others(517): Show |
chr11 | 77816144 | 77877352 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 1 | 1 | 4 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0001c0002t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0002c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| a0003c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0340 | EUR | GBR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0350 | EUR | GBR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0267 | EUR | GBR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0084 | EUR | FIN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | FIN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0080 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0050 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0238 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0064 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0042 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0265 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0277 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0280 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0341 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0040 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0261 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0041 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0242 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0035 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0247 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0024 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0322 | EUR | IBS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0278 | EUR | IBS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0244 | EUR | IBS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0329 | EUR | IBS | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0255 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0241 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0032 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0218 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0036 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0051 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0052 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | CDX | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0068 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0034 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0253 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0230 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0076 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0221 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0343 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0077 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0229 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0258 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0078 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0345 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0235 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0071 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0066 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0344 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0070 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0082 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0260 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0251 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0257 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0079 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0342 | AFR | ESN | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0072 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0075 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0227 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0239 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0274 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0272 | SAS | STU | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0264 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0249 | SAS | PJL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0246 | SAS | BEB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0271 | SAS | BEB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | STU | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0046 | EAS | CHB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0062 | EAS | CHB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18942 | hp2 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18946 | hp1 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18951 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18951 | hp2 | a0003 | c0005 | t0001 | g0115 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18965 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18972 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18986 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18990 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18991 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19003 | hp2 | a0002 | c0003 | t0001 | g0045 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19005 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0237 | AFR | LWK | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19062 | hp1 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19068 | hp1 | a0002 | c0003 | t0001 | g0054 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19078 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19081 | hp1 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19083 | hp2 | a0002 | c0004 | t0001 | g0030 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0089 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19087 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | YRI | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | ASW | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | ASW | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | TSI | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0243 | SAS | GIH | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0266 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0276 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0073 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | MSL | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | USA | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | USA | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0140 | REF | REF | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0281 | REF | REF | AAMDC_chr11_77816144_77877352 | AAMDC | chr11 | 77816144 | 77877352 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77872220 | G | A | 1 | a0002 | 69 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(66): Show |
missense_variant | MODERATE | c.274G>A | p.Val92Met | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 4/4 | 390/522 | 274/369 | 92/122 | chr11 | 77872220 | |||
| chr11:77872295 | G | A | 1 | a0003 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.349G>A | p.Val117Ile | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 4/4 | 465/522 | 349/369 | 117/122 | chr11 | 77872295 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77842592 | T | C | 2 | a0001c0002a0002c0003 | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
synonymous_variant | LOW | c.96T>C | p.Gly32Gly | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/4 | 212/522 | 96/369 | 32/122 | chr11 | 77842592 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77872330 | G | A | 1 | a0001c0002t0002 | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*15G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 4/4 | 15 | chr11 | 77872330 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77821260 | C | T | 9 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(6): Show | 9 | HG01934.hp1 HG02155.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+19C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77821260 | |||||||
| chr11:77821327 | C | G | 1 | a0001c0001t0001g0355 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-19+86C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77821327 | |||||||
| chr11:77821345 | T | G | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+104T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77821345 | |||||||
| chr11:77821417 | T | C | 86 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(83): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-19+176T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77821417 | |||||||
| chr11:77821662 | G | C | 86 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(83): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-19+421G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77821662 | |||||||
| chr11:77821710 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-19+469G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77821710 | |||||||
| chr11:77821996 | G | A | 13 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(10): Show | 13 | HG01934.hp1 HG02155.hp1 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+755G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77821996 | |||||||
| chr11:77822024 | T | G | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+783T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77822024 | |||||||
| chr11:77822414 | C | CA | 122 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-19+1194dupA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77822414 | ||||||
| chr11:77822414 | C | CAA | 76 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(73): Show | 79 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-19+1193_-19+1194d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77822414 | ||||||
| chr11:77822414 | C | CAAA | 13 | a0001c0001t0001g0102a0001c0002t0001g0015a0001c0002t0001g0016others(10): Show | 13 | HG01433.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+1192_-19+1194d others(5): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77822414 | ||||||
| chr11:77822414 | CA | C | 18 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0348others(15): Show | 18 | HG00099.hp1 HG00099.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19+1194delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77822414 | ||||||
| chr11:77822606 | G | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-19+1365G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77822606 | |||||||
| chr11:77822711 | G | A | 2 | a0001c0001t0001g0116a0003c0005t0001g0115 | 2 | NA18951.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-19+1470G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77822711 | |||||||
| chr11:77822796 | G | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | NA19004.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-19+1555G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77822796 | |||||||
| chr11:77822886 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19+1645G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77822886 | |||||||
| chr11:77822960 | A | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-19+1719A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77822960 | |||||||
| chr11:77823175 | A | T | 4 | a0001c0002t0002g0342a0001c0002t0002g0343a0001c0002t0002g0344others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1934A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823175 | |||||||
| chr11:77823214 | C | CA | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-19+1993dupA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77823214 | ||||||
| chr11:77823214 | C | CAA | 34 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0118others(31): Show | 34 | HG00544.hp1 HG01074.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+1992_-19+1993d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77823214 | ||||||
| chr11:77823214 | CAAA | C | 72 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0023others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-19+1991_-19+1993d others(5): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77823214 | ||||||
| chr11:77823239 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-19+1998T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823239 | |||||||
| chr11:77823258 | A | G | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+2017A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823258 | |||||||
| chr11:77823309 | A | G | 86 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(83): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-19+2068A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823309 | |||||||
| chr11:77823398 | G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(288): Show | 307 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-19+2157G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823398 | |||||||
| chr11:77823614 | CCTG | C | 80 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0023others(77): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-19+2374_-19+2376d others(5): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823614 | |||||||
| chr11:77823619 | CT | C | 68 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0023others(65): Show | 71 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-19+2379delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823619 | |||||||
| chr11:77823620 | T | A | 12 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0001g0093others(9): Show | 12 | HG00280.hp1 HG01243.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+2379T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823620 | |||||||
| chr11:77823621 | C | A | 80 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0023others(77): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-19+2380C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823621 | |||||||
| chr11:77823621 | C | CA | 139 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(136): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.-19+2401dupA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77823621 | ||||||
| chr11:77823621 | C | CAA | 14 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(11): Show | 14 | HG01074.hp2 HG01358.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+2400_-19+2401d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77823621 | ||||||
| chr11:77823621 | CA | C | 9 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0111others(6): Show | 9 | HG00323.hp1 HG01168.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+2401delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77823621 | ||||||
| chr11:77823744 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-19+2503A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823744 | |||||||
| chr11:77823833 | C | A | 1 | a0001c0002t0001g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-19+2592C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823833 | |||||||
| chr11:77823986 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-19+2745G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77823986 | |||||||
| chr11:77824143 | A | C | 1 | a0001c0002t0002g0274 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-19+2902A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77824143 | |||||||
| chr11:77824231 | T | A | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+2990T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77824231 | |||||||
| chr11:77824732 | G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | NA18971.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-19+3491G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77824732 | |||||||
| chr11:77824978 | G | T | 1 | a0001c0002t0002g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19+3737G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77824978 | |||||||
| chr11:77825081 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+3840C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825081 | |||||||
| chr11:77825106 | G | A | 5 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(2): Show | 5 | NA18969.hp1 NA18995.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+3865G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825106 | |||||||
| chr11:77825125 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+3884C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825125 | |||||||
| chr11:77825142 | G | A | 3 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096 | 3 | HG01243.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+3901G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825142 | |||||||
| chr11:77825213 | A | C | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-19+3972A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825213 | |||||||
| chr11:77825217 | T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(284): Show | 303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.-19+3976T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825217 | |||||||
| chr11:77825220 | G | A | 1 | a0002c0003t0001g0032 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-19+3979G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825220 | |||||||
| chr11:77825292 | T | A | 1 | a0001c0001t0001g0294 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-19+4051T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825292 | |||||||
| chr11:77825389 | G | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | NA19005.hp1 NA19068.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-19+4148G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825389 | |||||||
| chr11:77825395 | T | C | 158 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(155): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-19+4154T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825395 | |||||||
| chr11:77825499 | G | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02922.hp2 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+4258G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825499 | |||||||
| chr11:77825548 | T | A | 1 | a0001c0002t0002g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19+4307T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825548 | |||||||
| chr11:77825617 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-19+4376G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825617 | |||||||
| chr11:77825698 | G | GT | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0336others(4): Show | 7 | HG01074.hp2 NA18957.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+4470dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77825698 | ||||||
| chr11:77825720 | C | T | 3 | a0001c0001t0001g0290a0001c0001t0001g0334a0001c0001t0001g0335 | 3 | HG02615.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-19+4479C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825720 | |||||||
| chr11:77825731 | G | A | 24 | a0001c0002t0002g0009a0001c0002t0002g0206a0001c0002t0002g0216others(21): Show | 25 | HG00639.hp2 HG02055.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+4490G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825731 | |||||||
| chr11:77825801 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-19+4560C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825801 | |||||||
| chr11:77825840 | T | A | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0112others(68): Show | 73 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.-19+4599T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77825840 | |||||||
| chr11:77826134 | A | G | 1 | a0001c0002t0002g0272 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-19+4893A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77826134 | |||||||
| chr11:77826286 | C | T | 1 | a0001c0002t0002g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-19+5045C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77826286 | |||||||
| chr11:77826361 | C | CA | 70 | a0001c0002t0001g0018a0001c0002t0001g0067a0001c0002t0001g0069others(67): Show | 73 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-19+5131dupA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77826361 | ||||||
| chr11:77826587 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-19+5346G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77826587 | |||||||
| chr11:77826930 | C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+5689C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77826930 | |||||||
| chr11:77826995 | C | T | 1 | a0001c0002t0002g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19+5754C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77826995 | |||||||
| chr11:77827103 | CAAAAAA | C | 159 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(156): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-19+5871_-19+5876d others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77827103 | ||||||
| chr11:77827148 | C | T | 1 | a0002c0003t0001g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19+5907C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77827148 | |||||||
| chr11:77827152 | G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0199 | 5 | HG02451.hp2 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+5911G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77827152 | |||||||
| chr11:77827903 | G | A | 69 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074others(66): Show | 72 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-19+6662G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77827903 | |||||||
| chr11:77827904 | G | A | 286 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.-19+6663G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77827904 | |||||||
| chr11:77827912 | A | G | 161 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(158): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-19+6671A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77827912 | |||||||
| chr11:77827965 | G | A | 3 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0348 | 3 | HG02451.hp1 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+6724G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77827965 | |||||||
| chr11:77828039 | G | A | 69 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074others(66): Show | 72 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-19+6798G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828039 | |||||||
| chr11:77828146 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-19+6905G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828146 | |||||||
| chr11:77828370 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-19+7129C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828370 | |||||||
| chr11:77828390 | G | A | 3 | a0001c0002t0002g0239a0001c0002t0002g0240a0001c0002t0002g0341 | 3 | HG01070.hp1 HG01168.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-19+7149G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828390 | |||||||
| chr11:77828395 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-19+7154C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828395 | |||||||
| chr11:77828598 | G | A | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG01081.hp2 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-19+7357G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828598 | |||||||
| chr11:77828670 | GA | G | 10 | a0001c0001t0001g0198a0001c0002t0001g0014a0001c0002t0001g0023others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+7445delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77828670 | ||||||
| chr11:77828678 | A | T | 3 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0348 | 3 | HG02451.hp1 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+7437A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828678 | |||||||
| chr11:77828683 | A | G | 1 | a0001c0002t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-19+7442A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828683 | |||||||
| chr11:77828763 | G | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0120a0001c0001t0001g0138others(10): Show | 14 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+7522G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828763 | |||||||
| chr11:77828887 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-19+7646A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77828887 | |||||||
| chr11:77829201 | TTCACA | T | 160 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(157): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-19+7962_-19+7966d others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77829201 | ||||||
| chr11:77829312 | T | G | 1 | a0001c0002t0001g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-19+8071T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77829312 | |||||||
| chr11:77829364 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+8123C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77829364 | |||||||
| chr11:77829556 | A | G | 3 | a0002c0003t0001g0022a0002c0003t0001g0031a0002c0004t0001g0030 | 3 | NA18965.hp2 NA18967.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-19+8315A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77829556 | |||||||
| chr11:77829702 | C | A | 1 | a0002c0003t0001g0034 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-19+8461C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77829702 | |||||||
| chr11:77829903 | C | T | 80 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(77): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-19+8662C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77829903 | |||||||
| chr11:77830415 | C | T | 2 | a0002c0003t0001g0033a0002c0003t0001g0080 | 2 | HG00408.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-19+9174C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77830415 | |||||||
| chr11:77830470 | C | T | 6 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0001g0093others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+9229C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77830470 | |||||||
| chr11:77830537 | G | A | 1 | a0001c0002t0001g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-19+9296G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77830537 | |||||||
| chr11:77830652 | A | G | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-19+9411A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77830652 | |||||||
| chr11:77830987 | C | CA | 27 | a0001c0001t0001g0097a0001c0001t0001g0120a0001c0001t0001g0214others(24): Show | 28 | HG01168.hp1 HG01175.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19+9769dupA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77830987 | ||||||
| chr11:77830987 | C | CAA | 12 | a0001c0001t0001g0298a0001c0002t0002g0112a0001c0002t0002g0205others(9): Show | 12 | HG00544.hp2 HG00639.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+9768_-19+9769d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77830987 | ||||||
| chr11:77830987 | C | CAAA | 34 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(31): Show | 35 | HG00140.hp2 HG00673.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-19+9767_-19+9769d others(5): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77830987 | ||||||
| chr11:77830987 | C | CAAAA | 11 | a0001c0002t0002g0241a0001c0002t0002g0242a0001c0002t0002g0243others(8): Show | 11 | HG00099.hp1 HG00639.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+9766_-19+9769d others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77830987 | ||||||
| chr11:77830987 | CA | C | 16 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0151others(13): Show | 16 | HG00280.hp2 HG01243.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+9769delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77830987 | ||||||
| chr11:77830987 | CAA | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 109 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-19+9768_-19+9769d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77830987 | ||||||
| chr11:77830987 | CAAAAAA | C | 51 | a0002c0003t0001g0003a0002c0003t0001g0004a0002c0003t0001g0005others(48): Show | 54 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.-19+9764_-19+9769d others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77830987 | ||||||
| chr11:77830987 | CAAAAAAA | C | 16 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074others(13): Show | 16 | HG01081.hp1 HG02257.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+9763_-19+9769d others(9): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77830987 | ||||||
| chr11:77831019 | C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+9778C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831019 | |||||||
| chr11:77831074 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-19+9833C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831074 | |||||||
| chr11:77831254 | T | C | 3 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-19+10013T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831254 | |||||||
| chr11:77831309 | C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | NA18979.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-19+10068C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831309 | |||||||
| chr11:77831309 | CAT | C | 3 | a0001c0001t0001g0290a0001c0001t0001g0334a0001c0001t0001g0335 | 3 | HG02615.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-19+10070_-19+1007 others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77831309 | ||||||
| chr11:77831562 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-19+10321A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831562 | |||||||
| chr11:77831636 | A | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02135.hp1 NA18948.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-19+10395A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831636 | |||||||
| chr11:77831664 | A | C | 1 | a0001c0002t0001g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-19+10423A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831664 | |||||||
| chr11:77831694 | C | CT | 58 | a0001c0001t0001g0136a0001c0002t0001g0027a0001c0002t0001g0028others(55): Show | 61 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-19+10470dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77831694 | ||||||
| chr11:77831694 | CT | C | 23 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0121others(20): Show | 23 | HG00735.hp1 HG01074.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+10470delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77831694 | ||||||
| chr11:77831759 | G | A | 1 | a0002c0003t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-19+10518G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831759 | |||||||
| chr11:77831759 | G | T | 1 | a0001c0002t0001g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-19+10518G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831759 | |||||||
| chr11:77831862 | A | AT | 37 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0102others(34): Show | 39 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-18-10590dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77831862 | ||||||
| chr11:77831862 | AT | A | 136 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0153others(133): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-18-10590delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77831862 | ||||||
| chr11:77831862 | ATTTTTTT others(4): Show |
A | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG01074.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-18-10600_-18-1059 others(15): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77831862 | ||||||
| chr11:77831939 | A | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-18-10540A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77831939 | |||||||
| chr11:77832107 | C | G | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-10372C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832107 | |||||||
| chr11:77832267 | A | G | 3 | a0002c0003t0001g0060a0002c0003t0001g0061a0002c0003t0001g0062 | 3 | NA18747.hp1 NA18950.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-18-10212A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832267 | |||||||
| chr11:77832330 | CT | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.-18-10136delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832330 | ||||||
| chr11:77832412 | C | T | 2 | a0001c0002t0002g0217a0001c0002t0002g0222 | 2 | HG02074.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-18-10067C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832412 | |||||||
| chr11:77832475 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-18-10004C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832475 | |||||||
| chr11:77832553 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-18-9926G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832553 | |||||||
| chr11:77832618 | G | A | 1 | a0002c0003t0001g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18-9861G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832618 | |||||||
| chr11:77832697 | GA | G | 9 | a0001c0001t0001g0303a0001c0002t0001g0023a0001c0002t0001g0088others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-9768delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832697 | ||||||
| chr11:77832949 | ATATG | A | 10 | a0001c0002t0002g0216a0001c0002t0002g0217a0001c0002t0002g0233others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-9528_-18-9525d others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832949 | ||||||
| chr11:77832949 | ATATGTG | A | 44 | a0001c0002t0002g0010a0001c0002t0002g0222a0001c0002t0002g0230others(41): Show | 45 | HG00099.hp1 HG00673.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-18-9528_-18-9523d others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832949 | ||||||
| chr11:77832949 | ATATGTGT others(1): Show |
A | 18 | a0001c0002t0002g0009a0001c0002t0002g0112a0001c0002t0002g0205others(15): Show | 19 | HG00639.hp2 HG01496.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-9528_-18-9521d others(10): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832949 | ||||||
| chr11:77832949 | ATATGTGT others(3): Show |
A | 1 | a0001c0002t0002g0228 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-18-9528_-18-9519d others(12): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832949 | ||||||
| chr11:77832949 | ATATGTGT others(5): Show |
A | 1 | a0001c0002t0002g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-18-9528_-18-9517d others(14): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832949 | ||||||
| chr11:77832951 | A | ATG | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0288others(7): Show | 10 | HG00099.hp2 HG01167.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-9482_-18-9481d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | A | G | 4 | a0001c0001t0001g0290a0001c0001t0001g0303a0001c0001t0001g0334others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-9528A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832951 | |||||||
| chr11:77832951 | ATG | A | 13 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0211others(10): Show | 13 | HG01074.hp2 HG01261.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-9482_-18-9481d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | ATGTG | A | 8 | a0001c0001t0001g0199a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 8 | HG01243.hp2 HG01928.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-9484_-18-9481d others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | ATGTGTG | A | 16 | a0001c0001t0001g0002a0001c0001t0001g0106a0001c0001t0001g0136others(13): Show | 16 | HG00544.hp2 HG01081.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-9486_-18-9481d others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | ATGTGTGT others(1): Show |
A | 120 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0102others(117): Show | 123 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-18-9488_-18-9481d others(10): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | ATGTGTGT others(3): Show |
A | 41 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0098others(38): Show | 42 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.-18-9490_-18-9481d others(12): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | ATGTGTGT others(5): Show |
A | 10 | a0001c0001t0001g0006a0001c0001t0001g0139a0001c0001t0001g0141others(7): Show | 11 | HG00323.hp1 HG01071.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-9492_-18-9481d others(14): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | ATGTGTGT others(7): Show |
A | 11 | a0001c0001t0001g0121a0001c0001t0001g0133a0001c0001t0001g0138others(8): Show | 11 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-9494_-18-9481d others(16): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | ATGTGTGT others(9): Show |
A | 11 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0131others(8): Show | 11 | HG01975.hp1 HG02056.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-9496_-18-9481d others(18): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832951 | ATGTGTGT others(13): Show |
A | 1 | a0001c0001t0001g0347 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18-9500_-18-9481d others(22): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77832951 | ||||||
| chr11:77832953 | G | A | 1 | a0001c0002t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18-9526G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832953 | |||||||
| chr11:77832959 | G | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-18-9520G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832959 | |||||||
| chr11:77832961 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-18-9518G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832961 | |||||||
| chr11:77832989 | G | A | 10 | a0001c0001t0001g0114a0001c0002t0002g0216a0001c0002t0002g0217others(7): Show | 10 | HG02055.hp1 HG02074.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-9490G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832989 | |||||||
| chr11:77832991 | G | A | 138 | a0001c0001t0001g0106a0001c0001t0001g0113a0001c0001t0001g0114others(135): Show | 142 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-18-9488G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832991 | |||||||
| chr11:77832993 | G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.-18-9486G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832993 | |||||||
| chr11:77832995 | G | A | 277 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-18-9484G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832995 | |||||||
| chr11:77832997 | G | A | 286 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.-18-9482G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832997 | |||||||
| chr11:77832999 | A | G | 3 | a0001c0001t0001g0296a0001c0001t0001g0325a0001c0001t0001g0351 | 3 | HG01081.hp2 HG02083.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-18-9480A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77832999 | |||||||
| chr11:77833003 | A | T | 1 | a0001c0002t0001g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-9476A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833003 | |||||||
| chr11:77833004 | TA | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0360a0001c0002t0001g0093others(6): Show | 9 | HG01934.hp1 HG02056.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-9474delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833004 | |||||||
| chr11:77833005 | A | T | 5 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-9474A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833005 | |||||||
| chr11:77833006 | TA | T | 133 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0098others(130): Show | 138 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.-18-9472delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833006 | |||||||
| chr11:77833007 | A | T | 40 | a0001c0001t0001g0106a0001c0001t0001g0122a0001c0001t0001g0134others(37): Show | 40 | HG01070.hp1 HG01243.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18-9472A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833007 | |||||||
| chr11:77833008 | TA | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0167others(16): Show | 21 | HG00733.hp2 HG01081.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-9470delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833008 | |||||||
| chr11:77833009 | A | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.-18-9470A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833009 | |||||||
| chr11:77833009 | AT | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0133a0001c0001t0001g0153others(10): Show | 13 | HG00323.hp2 HG00735.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-9450delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77833009 | ||||||
| chr11:77833010 | T | TA | 4 | a0001c0001t0001g0290a0001c0001t0001g0304a0001c0001t0001g0335others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-9469_-18-9468i others(3): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833010 | |||||||
| chr11:77833011 | T | A | 12 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0121others(9): Show | 12 | HG02056.hp2 HG02148.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18-9468T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833011 | |||||||
| chr11:77833012 | T | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0204 | 2 | HG01975.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-18-9467T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833012 | |||||||
| chr11:77833064 | T | G | 1 | a0002c0003t0001g0039 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-18-9415T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833064 | |||||||
| chr11:77833184 | A | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0301a0001c0001t0001g0324 | 3 | HG00597.hp1 HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-18-9295A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833184 | |||||||
| chr11:77833298 | G | C | 2 | a0001c0001t0001g0116a0003c0005t0001g0115 | 2 | NA18951.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-18-9181G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833298 | |||||||
| chr11:77833897 | C | G | 3 | a0001c0001t0001g0290a0001c0001t0001g0334a0001c0001t0001g0335 | 3 | HG02615.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-8582C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77833897 | |||||||
| chr11:77834079 | C | T | 1 | a0002c0003t0001g0034 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-18-8400C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77834079 | |||||||
| chr11:77834248 | T | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0166 | 2 | HG00735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-18-8231T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77834248 | |||||||
| chr11:77834318 | A | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-18-8161A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77834318 | |||||||
| chr11:77834433 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18-8046T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77834433 | |||||||
| chr11:77834441 | G | GT | 129 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.-18-8017dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77834441 | ||||||
| chr11:77834441 | G | GTT | 10 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0147others(7): Show | 10 | HG00741.hp2 HG01123.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-8018_-18-8017d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77834441 | ||||||
| chr11:77834441 | GT | G | 117 | a0001c0001t0001g0295a0001c0002t0001g0014a0001c0002t0001g0017others(114): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-18-8017delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77834441 | ||||||
| chr11:77834762 | A | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.-18-7717A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77834762 | |||||||
| chr11:77834772 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18-7707G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77834772 | |||||||
| chr11:77834824 | A | C | 81 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0018others(78): Show | 84 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-18-7655A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77834824 | |||||||
| chr11:77835100 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-18-7379C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77835100 | |||||||
| chr11:77835305 | T | C | 1 | a0002c0003t0001g0040 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-18-7174T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77835305 | |||||||
| chr11:77835388 | C | G | 1 | a0001c0002t0001g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-18-7091C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77835388 | |||||||
| chr11:77835472 | C | CAT | 161 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(158): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-18-7005_-18-7004d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77835472 | ||||||
| chr11:77835722 | C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-18-6757C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77835722 | |||||||
| chr11:77835740 | G | A | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG00544.hp1 HG02027.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-6739G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77835740 | |||||||
| chr11:77835816 | G | A | 3 | a0001c0002t0002g0246a0001c0002t0002g0251a0001c0002t0002g0274 | 3 | HG03491.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-18-6663G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77835816 | |||||||
| chr11:77835922 | A | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0199others(5): Show | 10 | HG01496.hp2 HG01975.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-6557A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77835922 | |||||||
| chr11:77836460 | G | T | 3 | a0001c0002t0002g0262a0001c0002t0002g0263a0001c0002t0002g0270 | 3 | NA18955.hp1 NA18970.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-18-6019G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77836460 | |||||||
| chr11:77836636 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-18-5843T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77836636 | |||||||
| chr11:77836688 | G | T | 1 | a0001c0002t0002g0223 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-18-5791G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77836688 | |||||||
| chr11:77836691 | C | T | 25 | a0002c0003t0001g0020a0002c0003t0001g0022a0002c0003t0001g0031others(22): Show | 25 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-5788C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77836691 | |||||||
| chr11:77836997 | GTGTT | G | 3 | a0002c0003t0001g0060a0002c0003t0001g0061a0002c0003t0001g0062 | 3 | NA18747.hp1 NA18950.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-18-5478_-18-5475d others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77836997 | ||||||
| chr11:77837489 | CT | C | 80 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(77): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-18-4989delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77837489 | |||||||
| chr11:77837799 | AT | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-4679delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77837799 | |||||||
| chr11:77837891 | A | AAAAT | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-4568_-18-4565d others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77837891 | ||||||
| chr11:77838214 | T | TGTCTTGT others(3): Show |
45 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18-4265_-18-4264i others(12): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838214 | |||||||
| chr11:77838215 | A | T | 45 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18-4264A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838215 | |||||||
| chr11:77838217 | A | T | 45 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18-4262A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838217 | |||||||
| chr11:77838218 | C | G | 45 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18-4261C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838218 | |||||||
| chr11:77838220 | G | T | 45 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18-4259G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838220 | |||||||
| chr11:77838528 | T | C | 1 | a0001c0002t0002g0252 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-18-3951T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838528 | |||||||
| chr11:77838567 | T | C | 2 | a0001c0002t0001g0094a0001c0002t0001g0096 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-3912T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838567 | |||||||
| chr11:77838615 | C | CT | 7 | a0001c0001t0001g0106a0001c0001t0001g0336a0001c0002t0001g0014others(4): Show | 7 | HG02055.hp2 HG02056.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-3845dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77838615 | ||||||
| chr11:77838615 | C | CTT | 10 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0092others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-3846_-18-3845d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77838615 | ||||||
| chr11:77838615 | C | CTTT | 67 | a0001c0002t0001g0018a0001c0002t0001g0023a0001c0002t0001g0025others(64): Show | 70 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-18-3847_-18-3845d others(5): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77838615 | ||||||
| chr11:77838661 | G | C | 1 | a0001c0002t0002g0344 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-3818G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838661 | |||||||
| chr11:77838702 | C | T | 1 | a0001c0002t0002g0261 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-18-3777C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838702 | |||||||
| chr11:77838774 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-18-3705G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838774 | |||||||
| chr11:77838789 | T | C | 1 | a0002c0003t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18-3690T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838789 | |||||||
| chr11:77838829 | G | A | 25 | a0002c0003t0001g0020a0002c0003t0001g0022a0002c0003t0001g0031others(22): Show | 25 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-3650G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838829 | |||||||
| chr11:77838856 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18-3623T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838856 | |||||||
| chr11:77838858 | C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-3621C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838858 | |||||||
| chr11:77838895 | C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-18-3584C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838895 | |||||||
| chr11:77838907 | C | T | 6 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0001g0093others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-3572C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77838907 | |||||||
| chr11:77839421 | A | G | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG01074.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-18-3058A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77839421 | |||||||
| chr11:77839551 | G | A | 2 | a0001c0002t0002g0206a0001c0002t0002g0218 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-18-2928G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77839551 | |||||||
| chr11:77839734 | G | C | 158 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(155): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-18-2745G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77839734 | |||||||
| chr11:77839908 | A | T | 3 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096 | 3 | HG01243.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-2571A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77839908 | |||||||
| chr11:77839942 | G | A | 2 | a0001c0002t0002g0344a0001c0002t0002g0345 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-18-2537G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77839942 | |||||||
| chr11:77840050 | G | A | 72 | a0001c0002t0001g0017a0001c0002t0001g0023a0001c0002t0001g0025others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-18-2429G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77840050 | |||||||
| chr11:77840097 | AAC | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.-18-2360_-18-2359d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 77840097 | ||||||
| chr11:77840106 | A | G | 1 | a0002c0003t0001g0019 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-18-2373A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77840106 | |||||||
| chr11:77840115 | C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0203 | 2 | HG00140.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-18-2364C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77840115 | |||||||
| chr11:77840250 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-18-2229A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77840250 | |||||||
| chr11:77840257 | A | G | 9 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(6): Show | 9 | HG01934.hp1 HG02155.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-2222A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77840257 | |||||||
| chr11:77840454 | C | T | 45 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18-2025C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77840454 | |||||||
| chr11:77840455 | G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0306others(1): Show | 4 | HG00099.hp2 HG01069.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-2024G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77840455 | |||||||
| chr11:77841012 | C | T | 1 | a0002c0003t0001g0052 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-18-1467C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77841012 | |||||||
| chr11:77841471 | C | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-1008C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77841471 | |||||||
| chr11:77841488 | A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-18-991A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77841488 | |||||||
| chr11:77841511 | CA | C | 4 | a0001c0002t0002g0342a0001c0002t0002g0343a0001c0002t0002g0344others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-967delA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77841511 | |||||||
| chr11:77841566 | C | T | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-18-913C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77841566 | |||||||
| chr11:77841941 | T | C | 69 | a0001c0002t0001g0018a0001c0002t0001g0067a0001c0002t0001g0069others(66): Show | 72 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-18-538T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77841941 | |||||||
| chr11:77841984 | C | T | 45 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-18-495C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77841984 | |||||||
| chr11:77842128 | G | C | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-351G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77842128 | |||||||
| chr11:77842250 | T | C | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-18-229T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77842250 | |||||||
| chr11:77842320 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-18-159T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77842320 | |||||||
| chr11:77842363 | G | A | 4 | a0001c0002t0002g0342a0001c0002t0002g0343a0001c0002t0002g0344others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-116G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 1/3 | chr11 | 77842363 | |||||||
| chr11:77843005 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.132+377T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843005 | |||||||
| chr11:77843111 | C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.132+483C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843111 | |||||||
| chr11:77843305 | T | C | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG01074.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.132+677T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843305 | |||||||
| chr11:77843591 | A | G | 1 | a0002c0003t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.132+963A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843591 | |||||||
| chr11:77843775 | G | A | 159 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(156): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.132+1147G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843775 | |||||||
| chr11:77843885 | G | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.132+1257G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843885 | |||||||
| chr11:77843899 | G | T | 68 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074others(65): Show | 71 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+1271G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843899 | |||||||
| chr11:77843934 | C | T | 1 | a0001c0002t0002g0341 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.132+1306C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843934 | |||||||
| chr11:77843939 | T | C | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.132+1311T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77843939 | |||||||
| chr11:77844204 | A | C | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.132+1576A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844204 | |||||||
| chr11:77844310 | A | G | 286 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.132+1682A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844310 | |||||||
| chr11:77844406 | A | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0109 | 4 | HG02451.hp2 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1778A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844406 | |||||||
| chr11:77844435 | G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0307 | 2 | NA18939.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.132+1807G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844435 | |||||||
| chr11:77844778 | C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 111 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.132+2150C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844778 | |||||||
| chr11:77844799 | A | T | 1 | a0002c0003t0001g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.132+2171A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844799 | |||||||
| chr11:77844845 | T | G | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.132+2217T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844845 | |||||||
| chr11:77844986 | T | C | 5 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(2): Show | 5 | HG00639.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+2358T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844986 | |||||||
| chr11:77844997 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132+2369T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77844997 | |||||||
| chr11:77845444 | T | TG | 45 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.132+2823dupG | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77845444 | ||||||
| chr11:77845470 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.132+2842A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77845470 | |||||||
| chr11:77845589 | T | A | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.132+2961T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77845589 | |||||||
| chr11:77845609 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.132+2981T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77845609 | |||||||
| chr11:77845787 | G | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.132+3159G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77845787 | |||||||
| chr11:77845994 | G | C | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.132+3366G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77845994 | |||||||
| chr11:77846007 | AT | A | 8 | a0001c0001t0001g0283a0001c0001t0001g0288a0001c0001t0001g0307others(5): Show | 8 | HG01975.hp2 HG02071.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+3390delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77846007 | ||||||
| chr11:77846057 | C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.132+3429C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77846057 | |||||||
| chr11:77847052 | A | T | 2 | a0001c0002t0002g0112a0001c0002t0002g0205 | 2 | HG01496.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.132+4424A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77847052 | |||||||
| chr11:77847172 | ACT | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.132+4547_132+4548d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77847172 | ||||||
| chr11:77847207 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.132+4579T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77847207 | |||||||
| chr11:77847604 | A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0152a0001c0001t0001g0181others(2): Show | 6 | HG02132.hp1 NA18968.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+4976A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77847604 | |||||||
| chr11:77847703 | G | T | 1 | a0001c0002t0001g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.132+5075G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77847703 | |||||||
| chr11:77847965 | G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.132+5337G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77847965 | |||||||
| chr11:77847988 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.132+5360T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77847988 | |||||||
| chr11:77848176 | G | T | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+5548G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848176 | |||||||
| chr11:77848177 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+5549A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848177 | |||||||
| chr11:77848236 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.132+5608T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848236 | |||||||
| chr11:77848264 | A | T | 1 | a0001c0001t0001g0188 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.132+5636A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848264 | |||||||
| chr11:77848348 | A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0199 | 5 | HG02451.hp2 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+5720A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848348 | |||||||
| chr11:77848427 | G | A | 4 | a0001c0002t0002g0342a0001c0002t0002g0343a0001c0002t0002g0344others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+5799G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848427 | |||||||
| chr11:77848567 | C | A | 5 | a0001c0002t0002g0252a0001c0002t0002g0253a0001c0002t0002g0254others(2): Show | 5 | HG02027.hp1 HG02273.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+5939C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848567 | |||||||
| chr11:77848658 | C | T | 1 | a0001c0002t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.132+6030C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848658 | |||||||
| chr11:77848739 | A | G | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.132+6111A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77848739 | |||||||
| chr11:77849026 | A | G | 165 | a0001c0001t0001g0212a0001c0001t0001g0319a0001c0001t0001g0320others(162): Show | 170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.132+6398A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849026 | |||||||
| chr11:77849038 | CT | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0174a0001c0001t0001g0347others(3): Show | 6 | HG01070.hp2 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+6425delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77849038 | ||||||
| chr11:77849256 | G | A | 1 | a0002c0003t0001g0044 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.132+6628G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849256 | |||||||
| chr11:77849277 | G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.132+6649G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849277 | |||||||
| chr11:77849283 | G | A | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.132+6655G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849283 | |||||||
| chr11:77849308 | G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.132+6680G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849308 | |||||||
| chr11:77849476 | G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02922.hp2 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.132+6848G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849476 | |||||||
| chr11:77849552 | G | C | 1 | a0001c0002t0002g0255 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.132+6924G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849552 | |||||||
| chr11:77849606 | G | T | 75 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0112others(72): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.132+6978G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849606 | |||||||
| chr11:77849613 | C | A | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.132+6985C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77849613 | |||||||
| chr11:77849762 | ATCTT | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0148a0001c0001t0001g0175others(2): Show | 5 | NA18970.hp1 NA18973.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+7141_132+7144d others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77849762 | ||||||
| chr11:77850033 | A | G | 6 | a0001c0001t0001g0158a0001c0001t0001g0167a0001c0001t0001g0170others(3): Show | 6 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+7405A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77850033 | |||||||
| chr11:77850129 | C | T | 4 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG02280.hp1 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+7501C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77850129 | |||||||
| chr11:77850209 | T | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.132+7581T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77850209 | |||||||
| chr11:77850333 | G | A | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.132+7705G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77850333 | |||||||
| chr11:77850434 | C | T | 6 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0001g0093others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+7806C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77850434 | |||||||
| chr11:77850765 | CACACACA others(13): Show |
C | 2 | a0001c0002t0002g0112a0001c0002t0002g0205 | 2 | HG01496.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.132+8147_132+8166d others(22): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77850765 | ||||||
| chr11:77850769 | CACACATA others(9): Show |
C | 4 | a0001c0002t0002g0342a0001c0002t0002g0343a0001c0002t0002g0344others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+8147_132+8162d others(18): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77850769 | ||||||
| chr11:77850775 | TACACACA others(9): Show |
T | 69 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0206others(66): Show | 71 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.132+8157_132+8172d others(18): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77850775 | ||||||
| chr11:77850785 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.132+8157T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77850785 | |||||||
| chr11:77850785 | TACACAC | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 219 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.132+8173_132+8178d others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77850785 | ||||||
| chr11:77850855 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.132+8227G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77850855 | |||||||
| chr11:77850953 | C | CT | 11 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0155others(8): Show | 11 | HG00735.hp1 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.132+8345dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77850953 | ||||||
| chr11:77850953 | C | CTT | 120 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 125 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.132+8344_132+8345d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77850953 | ||||||
| chr11:77850953 | CT | C | 9 | a0001c0001t0001g0311a0001c0001t0001g0347a0001c0002t0001g0015others(6): Show | 9 | HG01074.hp2 HG01928.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+8345delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77850953 | ||||||
| chr11:77850987 | G | A | 156 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(153): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.132+8359G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77850987 | |||||||
| chr11:77851004 | G | A | 1 | a0001c0002t0002g0250 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+8376G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851004 | |||||||
| chr11:77851018 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.132+8390C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851018 | |||||||
| chr11:77851025 | G | A | 4 | a0001c0002t0001g0017a0001c0002t0001g0023a0001c0002t0001g0025others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+8397G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851025 | |||||||
| chr11:77851137 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.132+8509T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851137 | |||||||
| chr11:77851165 | G | A | 2 | a0001c0002t0002g0206a0001c0002t0002g0218 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.132+8537G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851165 | |||||||
| chr11:77851180 | C | G | 2 | a0001c0002t0002g0248a0001c0002t0002g0340 | 2 | HG00099.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.132+8552C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851180 | |||||||
| chr11:77851248 | C | T | 1 | a0001c0002t0002g0245 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.132+8620C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851248 | |||||||
| chr11:77851789 | T | A | 5 | a0001c0002t0002g0223a0001c0002t0002g0224a0001c0002t0002g0225others(2): Show | 5 | HG00639.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+9161T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851789 | |||||||
| chr11:77851926 | A | T | 2 | a0001c0001t0001g0356a0001c0001t0001g0361 | 2 | NA18940.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.132+9298A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851926 | |||||||
| chr11:77851995 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.132+9367C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77851995 | |||||||
| chr11:77852043 | C | T | 1 | a0001c0002t0001g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.132+9415C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77852043 | |||||||
| chr11:77852224 | C | CA | 76 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.132+9613dupA | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAA | 12 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0111others(9): Show | 12 | HG00099.hp1 HG00639.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.132+9610_132+9613d others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAA | 33 | a0001c0002t0001g0017a0001c0002t0001g0028a0001c0002t0001g0029others(30): Show | 34 | HG00639.hp2 HG02055.hp2 HG02273.hp2 others(31): Show |
intron_variant | MODIFIER | c.132+9609_132+9613d others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAA | 95 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(92): Show | 99 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.132+9608_132+9613d others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA | 21 | a0001c0002t0002g0269a0002c0003t0001g0019a0002c0003t0001g0020others(18): Show | 21 | HG00408.hp1 HG00597.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.132+9607_132+9613d others(9): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.132+9603_132+9613d others(13): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.132+9602_132+9613d others(14): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA others(7): Show |
12 | a0001c0001t0001g0116a0001c0001t0001g0131a0001c0001t0001g0133others(9): Show | 12 | HG00735.hp1 HG01074.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+9600_132+9613d others(16): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA others(8): Show |
42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 45 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.132+9599_132+9613d others(17): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA others(9): Show |
48 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0100others(45): Show | 50 | HG00544.hp1 HG00735.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.132+9598_132+9613d others(18): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA others(10): Show |
12 | a0001c0001t0001g0122a0001c0001t0001g0138a0001c0001t0001g0141others(9): Show | 12 | HG00323.hp1 HG00423.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.132+9597_132+9613d others(19): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0127a0001c0001t0001g0146 | 3 | HG02257.hp1 NA19082.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.132+9613_132+9614i others(20): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852224 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0144 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.132+9613_132+9614i others(21): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852224 | ||||||
| chr11:77852239 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.132+9613_132+9614i others(18): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77852239 | ||||||
| chr11:77852242 | G | A | 157 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(154): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.132+9614G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77852242 | |||||||
| chr11:77852298 | C | T | 150 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(147): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.132+9670C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77852298 | |||||||
| chr11:77852575 | G | A | 2 | a0002c0003t0001g0060a0002c0003t0001g0061 | 2 | NA18950.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.132+9947G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77852575 | |||||||
| chr11:77852635 | A | G | 2 | a0001c0001t0001g0116a0003c0005t0001g0115 | 2 | NA18951.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.132+10007A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77852635 | |||||||
| chr11:77852741 | A | T | 289 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(286): Show | 299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.132+10113A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77852741 | |||||||
| chr11:77852785 | T | C | 6 | a0001c0002t0002g0112a0001c0002t0002g0205a0001c0002t0002g0342others(3): Show | 6 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+10157T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77852785 | |||||||
| chr11:77853094 | G | C | 5 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(2): Show | 5 | HG01243.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+10466G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77853094 | |||||||
| chr11:77853221 | A | G | 19 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(16): Show | 20 | HG00673.hp2 HG02027.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.132+10593A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77853221 | |||||||
| chr11:77853423 | T | C | 4 | a0001c0002t0002g0243a0001c0002t0002g0246a0001c0002t0002g0251others(1): Show | 4 | HG03491.hp2 HG03669.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+10795T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77853423 | |||||||
| chr11:77853562 | C | T | 1 | a0002c0003t0001g0084 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.132+10934C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77853562 | |||||||
| chr11:77853617 | C | G | 1 | a0001c0001t0001g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.132+10989C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77853617 | |||||||
| chr11:77853993 | C | CT | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(196): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.132+11380dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77853993 | ||||||
| chr11:77853993 | CT | C | 69 | a0001c0002t0001g0014a0001c0002t0002g0009a0001c0002t0002g0010others(66): Show | 71 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.132+11380delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77853993 | ||||||
| chr11:77853993 | CTT | C | 6 | a0001c0002t0002g0112a0001c0002t0002g0205a0001c0002t0002g0342others(3): Show | 6 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+11379_132+1138 others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77853993 | ||||||
| chr11:77854066 | C | A | 1 | a0001c0002t0002g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.132+11438C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854066 | |||||||
| chr11:77854092 | A | T | 1 | a0001c0001t0001g0310 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.132+11464A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854092 | |||||||
| chr11:77854135 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.132+11507C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854135 | |||||||
| chr11:77854183 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132+11555G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854183 | |||||||
| chr11:77854587 | C | T | 3 | a0001c0002t0002g0247a0001c0002t0002g0265a0001c0002t0002g0280 | 3 | HG00733.hp2 HG01167.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.132+11959C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854587 | |||||||
| chr11:77854633 | C | A | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.132+12005C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854633 | |||||||
| chr11:77854668 | T | C | 1 | a0001c0002t0002g0256 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.132+12040T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854668 | |||||||
| chr11:77854676 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.132+12048C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854676 | |||||||
| chr11:77854831 | C | T | 68 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074others(65): Show | 71 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+12203C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77854831 | |||||||
| chr11:77855008 | A | G | 72 | a0001c0002t0001g0017a0001c0002t0001g0023a0001c0002t0001g0025others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.132+12380A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855008 | |||||||
| chr11:77855311 | A | T | 157 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(154): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.132+12683A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855311 | |||||||
| chr11:77855478 | C | A | 2 | a0001c0002t0002g0342a0001c0002t0002g0343 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.132+12850C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855478 | |||||||
| chr11:77855531 | G | A | 1 | a0001c0002t0002g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.132+12903G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855531 | |||||||
| chr11:77855551 | G | A | 1 | a0002c0003t0001g0045 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.132+12923G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855551 | |||||||
| chr11:77855604 | C | T | 6 | a0001c0002t0002g0112a0001c0002t0002g0205a0001c0002t0002g0342others(3): Show | 6 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+12976C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855604 | |||||||
| chr11:77855720 | C | CT | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(313): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.132+13109dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77855720 | ||||||
| chr11:77855720 | C | CTT | 35 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0114others(32): Show | 35 | HG01243.hp1 HG01256.hp1 HG02027.hp2 others(32): Show |
intron_variant | MODIFIER | c.132+13108_132+1310 others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77855720 | ||||||
| chr11:77855758 | G | C | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.132+13130G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855758 | |||||||
| chr11:77855776 | A | C | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.132+13148A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855776 | |||||||
| chr11:77855803 | A | G | 159 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(156): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.132+13175A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855803 | |||||||
| chr11:77855877 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.132+13249G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855877 | |||||||
| chr11:77855952 | T | C | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | HG01074.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.132+13324T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77855952 | |||||||
| chr11:77856164 | C | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 132 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.132+13536C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77856164 | |||||||
| chr11:77856193 | G | A | 4 | a0001c0002t0002g0342a0001c0002t0002g0343a0001c0002t0002g0344others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-13529G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77856193 | |||||||
| chr11:77856388 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.133-13334T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77856388 | |||||||
| chr11:77856482 | C | T | 78 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(75): Show | 80 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.133-13240C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77856482 | |||||||
| chr11:77856538 | G | A | 68 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074others(65): Show | 71 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.133-13184G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77856538 | |||||||
| chr11:77856635 | C | T | 159 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(156): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.133-13087C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77856635 | |||||||
| chr11:77856834 | G | A | 1 | a0001c0002t0002g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.133-12888G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77856834 | |||||||
| chr11:77856968 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.133-12754T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77856968 | |||||||
| chr11:77857319 | C | G | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.133-12403C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77857319 | |||||||
| chr11:77857618 | T | C | 1 | a0001c0002t0001g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.133-12104T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77857618 | |||||||
| chr11:77857699 | G | GT | 7 | a0001c0001t0001g0352a0001c0001t0001g0355a0001c0002t0002g0009others(4): Show | 8 | HG01256.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.133-12008dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77857699 | ||||||
| chr11:77857753 | T | C | 12 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.133-11969T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77857753 | |||||||
| chr11:77857757 | C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133-11965C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77857757 | |||||||
| chr11:77857844 | G | A | 1 | a0002c0003t0001g0055 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.133-11878G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77857844 | |||||||
| chr11:77857982 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.133-11740A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77857982 | |||||||
| chr11:77857989 | C | T | 75 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0112others(72): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.133-11733C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77857989 | |||||||
| chr11:77858064 | G | T | 82 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(79): Show | 85 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.133-11658G>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858064 | |||||||
| chr11:77858067 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.133-11655G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858067 | |||||||
| chr11:77858132 | C | T | 4 | a0001c0002t0001g0017a0001c0002t0001g0023a0001c0002t0001g0025others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-11590C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858132 | |||||||
| chr11:77858174 | A | G | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.133-11548A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858174 | |||||||
| chr11:77858194 | A | AT | 6 | a0001c0001t0001g0013a0001c0001t0001g0283a0001c0001t0001g0284others(3): Show | 7 | HG01192.hp2 HG01928.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-11510dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858194 | ||||||
| chr11:77858194 | AT | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 179 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.133-11510delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858194 | ||||||
| chr11:77858194 | ATT | A | 110 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(107): Show | 112 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.133-11511_133-1151 others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858194 | ||||||
| chr11:77858302 | C | CT | 76 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0102others(73): Show | 78 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.133-11395dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858302 | ||||||
| chr11:77858302 | C | CTT | 8 | a0001c0001t0001g0122a0001c0001t0001g0134a0001c0001t0001g0135others(5): Show | 8 | HG00733.hp1 HG02027.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.133-11396_133-1139 others(6): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858302 | ||||||
| chr11:77858302 | C | CTTT | 33 | a0001c0001t0001g0152a0001c0002t0001g0023a0001c0002t0001g0026others(30): Show | 34 | HG00099.hp1 HG00639.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.133-11397_133-1139 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858302 | ||||||
| chr11:77858302 | C | CTTTT | 38 | a0001c0002t0001g0025a0001c0002t0002g0010a0001c0002t0002g0217others(35): Show | 39 | HG00140.hp2 HG00639.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.133-11398_133-1139 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858302 | ||||||
| chr11:77858302 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.133-11404_133-1139 others(14): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858302 | ||||||
| chr11:77858302 | C | CTTTTTTT others(5): Show |
1 | a0001c0002t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.133-11406_133-1139 others(16): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858302 | ||||||
| chr11:77858302 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133-11407_133-1139 others(17): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858302 | ||||||
| chr11:77858302 | CT | C | 13 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0114others(10): Show | 13 | HG01168.hp1 HG01243.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-11395delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858302 | ||||||
| chr11:77858346 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.133-11376A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858346 | |||||||
| chr11:77858403 | C | CGGCTCGA others(5): Show |
82 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(79): Show | 85 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.133-11308_133-1130 others(16): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77858403 | ||||||
| chr11:77858432 | G | A | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.133-11290G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858432 | |||||||
| chr11:77858679 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.133-11043G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858679 | |||||||
| chr11:77858738 | T | C | 160 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(157): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.133-10984T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858738 | |||||||
| chr11:77858832 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.133-10890G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858832 | |||||||
| chr11:77858908 | A | C | 6 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0001g0093others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-10814A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858908 | |||||||
| chr11:77858913 | G | A | 1 | a0002c0003t0001g0034 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.133-10809G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858913 | |||||||
| chr11:77858938 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.133-10784G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77858938 | |||||||
| chr11:77859174 | A | G | 1 | a0001c0001t0001g0323 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.133-10548A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77859174 | |||||||
| chr11:77859257 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.133-10465G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77859257 | |||||||
| chr11:77859355 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.133-10367T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77859355 | |||||||
| chr11:77859392 | A | G | 6 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0001g0093others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-10330A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77859392 | |||||||
| chr11:77859552 | G | A | 1 | a0002c0003t0001g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.133-10170G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77859552 | |||||||
| chr11:77859681 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.133-10041A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77859681 | |||||||
| chr11:77859926 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.133-9796C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77859926 | |||||||
| chr11:77860085 | G | A | 1 | a0001c0002t0002g0223 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.133-9637G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77860085 | |||||||
| chr11:77860165 | G | C | 1 | a0001c0002t0002g0272 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.133-9557G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77860165 | |||||||
| chr11:77860907 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.133-8815C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77860907 | |||||||
| chr11:77860944 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.133-8778G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77860944 | |||||||
| chr11:77861114 | T | C | 1 | a0001c0002t0001g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.133-8608T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77861114 | |||||||
| chr11:77861422 | C | T | 78 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(75): Show | 80 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.133-8300C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77861422 | |||||||
| chr11:77861435 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.133-8287A>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77861435 | |||||||
| chr11:77861475 | C | A | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG01081.hp2 HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.133-8247C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77861475 | |||||||
| chr11:77861575 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.133-8147C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77861575 | |||||||
| chr11:77861598 | C | A | 1 | a0002c0003t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.133-8124C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77861598 | |||||||
| chr11:77861671 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.133-8051A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77861671 | |||||||
| chr11:77862110 | A | T | 1 | a0001c0002t0002g0262 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.133-7612A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77862110 | |||||||
| chr11:77862161 | G | A | 185 | a0001c0001t0001g0006a0001c0001t0001g0098a0001c0001t0001g0099others(182): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.133-7561G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77862161 | |||||||
| chr11:77862206 | T | A | 1 | a0001c0001t0001g0326 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.133-7516T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77862206 | |||||||
| chr11:77862497 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.133-7225G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77862497 | |||||||
| chr11:77862685 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.133-7037C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77862685 | |||||||
| chr11:77862761 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.133-6961G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77862761 | |||||||
| chr11:77863025 | G | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0202 | 2 | HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.133-6697G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863025 | |||||||
| chr11:77863076 | G | A | 1 | a0001c0002t0002g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.133-6646G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863076 | |||||||
| chr11:77863203 | C | T | 78 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(75): Show | 80 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.133-6519C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863203 | |||||||
| chr11:77863264 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.133-6458C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863264 | |||||||
| chr11:77863269 | A | G | 1 | a0001c0002t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.133-6453A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863269 | |||||||
| chr11:77863559 | C | T | 157 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(154): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.133-6163C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863559 | |||||||
| chr11:77863591 | G | C | 69 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0206others(66): Show | 71 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.133-6131G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863591 | |||||||
| chr11:77863616 | T | C | 2 | a0002c0003t0001g0068a0002c0003t0001g0070 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.133-6106T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863616 | |||||||
| chr11:77863651 | T | A | 157 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(154): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.133-6071T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863651 | |||||||
| chr11:77863864 | G | A | 9 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(6): Show | 9 | HG01934.hp1 HG02155.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.133-5858G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77863864 | |||||||
| chr11:77863933 | C | CT | 10 | a0001c0001t0001g0133a0001c0001t0001g0293a0001c0002t0001g0027others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-5779dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77863933 | ||||||
| chr11:77864085 | C | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | HG01074.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.133-5637C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864085 | |||||||
| chr11:77864151 | T | A | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.133-5571T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864151 | |||||||
| chr11:77864193 | T | G | 1 | a0001c0002t0002g0345 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.133-5529T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864193 | |||||||
| chr11:77864220 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.133-5502C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864220 | |||||||
| chr11:77864317 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.133-5405G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864317 | |||||||
| chr11:77864364 | C | T | 1 | a0002c0003t0001g0033 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.133-5358C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864364 | |||||||
| chr11:77864365 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.133-5357G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864365 | |||||||
| chr11:77864481 | G | A | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.133-5241G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864481 | |||||||
| chr11:77864593 | C | T | 157 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(154): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.133-5129C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864593 | |||||||
| chr11:77864595 | G | A | 71 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(68): Show | 74 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.133-5127G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864595 | |||||||
| chr11:77864619 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.133-5103A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864619 | |||||||
| chr11:77864629 | T | G | 6 | a0001c0002t0002g0112a0001c0002t0002g0205a0001c0002t0002g0342others(3): Show | 6 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-5093T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864629 | |||||||
| chr11:77864666 | G | A | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.133-5056G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864666 | |||||||
| chr11:77864751 | G | A | 6 | a0001c0002t0002g0112a0001c0002t0002g0205a0001c0002t0002g0342others(3): Show | 6 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-4971G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864751 | |||||||
| chr11:77864931 | T | C | 286 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.133-4791T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864931 | |||||||
| chr11:77864946 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.133-4776C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77864946 | |||||||
| chr11:77865158 | C | T | 1 | a0001c0002t0002g0262 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.133-4564C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77865158 | |||||||
| chr11:77865179 | T | C | 1 | a0001c0002t0002g0273 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.133-4543T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77865179 | |||||||
| chr11:77865801 | T | G | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.133-3921T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77865801 | |||||||
| chr11:77866448 | C | T | 76 | a0001c0002t0001g0014a0001c0002t0002g0009a0001c0002t0002g0010others(73): Show | 78 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.133-3274C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77866448 | |||||||
| chr11:77866450 | A | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.133-3272A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77866450 | |||||||
| chr11:77866800 | A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.133-2922A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77866800 | |||||||
| chr11:77866818 | C | A | 158 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(155): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.133-2904C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77866818 | |||||||
| chr11:77866931 | C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0131a0001c0001t0001g0162 | 3 | NA19011.hp2 NA19063.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.133-2791C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77866931 | |||||||
| chr11:77867187 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.133-2535G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77867187 | |||||||
| chr11:77867312 | AT | A | 155 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(152): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.133-2408delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77867312 | ||||||
| chr11:77867339 | C | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0323 | 3 | NA18954.hp2 NA18988.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.133-2383C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77867339 | |||||||
| chr11:77867494 | T | C | 19 | a0001c0002t0002g0009a0001c0002t0002g0206a0001c0002t0002g0216others(16): Show | 20 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.133-2228T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77867494 | |||||||
| chr11:77867584 | G | A | 2 | a0001c0002t0002g0344a0001c0002t0002g0345 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.133-2138G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77867584 | |||||||
| chr11:77867915 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.133-1807A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77867915 | |||||||
| chr11:77867960 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.133-1762T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77867960 | |||||||
| chr11:77868058 | C | CT | 79 | a0001c0001t0001g0158a0001c0001t0001g0189a0001c0001t0001g0314others(76): Show | 81 | HG00140.hp2 HG00673.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.133-1649dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77868058 | ||||||
| chr11:77868058 | C | CTT | 75 | a0001c0002t0001g0017a0001c0002t0001g0023a0001c0002t0001g0025others(72): Show | 78 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.133-1650_133-1649d others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77868058 | ||||||
| chr11:77868087 | G | A | 2 | a0001c0002t0002g0257a0001c0002t0002g0260 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.133-1635G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868087 | |||||||
| chr11:77868132 | T | C | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133-1590T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868132 | |||||||
| chr11:77868181 | G | A | 1 | a0001c0001t0001g0362 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.133-1541G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868181 | |||||||
| chr11:77868343 | C | T | 3 | a0001c0002t0002g0261a0001c0002t0002g0266a0001c0002t0002g0267 | 3 | HG00140.hp2 HG01123.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.133-1379C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868343 | |||||||
| chr11:77868357 | C | CT | 80 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0160others(77): Show | 85 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.133-1347dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77868357 | ||||||
| chr11:77868399 | C | T | 1 | a0001c0002t0002g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.133-1323C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868399 | |||||||
| chr11:77868507 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.133-1215C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868507 | |||||||
| chr11:77868695 | G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0199 | 5 | HG02451.hp2 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-1027G>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868695 | |||||||
| chr11:77868698 | GTTT | G | 15 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-1020_133-1018d others(5): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77868698 | ||||||
| chr11:77868701 | T | G | 67 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0206others(64): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.133-1021T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868701 | |||||||
| chr11:77868807 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133-915C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868807 | |||||||
| chr11:77868994 | T | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0134a0001c0001t0001g0135others(17): Show | 21 | HG00408.hp2 HG00609.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.133-728T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77868994 | |||||||
| chr11:77869100 | C | T | 1 | a0002c0003t0001g0087 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.133-622C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869100 | |||||||
| chr11:77869123 | C | A | 1 | a0001c0002t0002g0259 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.133-599C>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869123 | |||||||
| chr11:77869169 | T | C | 1 | a0002c0003t0001g0076 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.133-553T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869169 | |||||||
| chr11:77869194 | AT | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.133-524delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77869194 | ||||||
| chr11:77869302 | A | ATC | 40 | a0001c0002t0002g0010a0001c0002t0002g0217a0001c0002t0002g0222others(37): Show | 41 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.133-416_133-415dup others(2): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77869302 | ||||||
| chr11:77869305 | T | A | 1 | a0001c0001t0001g0191 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.133-417T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869305 | |||||||
| chr11:77869306 | C | CTT | 24 | a0001c0002t0002g0009a0001c0002t0002g0112a0001c0002t0002g0205others(21): Show | 25 | HG00639.hp2 HG01496.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.133-412_133-411dup others(2): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77869306 | ||||||
| chr11:77869306 | C | CTTT | 6 | a0001c0002t0002g0216a0001c0002t0002g0224a0001c0002t0002g0226others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-413_133-411dup others(3): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77869306 | ||||||
| chr11:77869307 | T | TC | 3 | a0001c0002t0002g0251a0001c0002t0002g0280a0001c0002t0002g0341 | 3 | HG01167.hp2 HG01168.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.133-415_133-414ins others(1): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869307 | |||||||
| chr11:77869308 | T | C | 3 | a0001c0002t0002g0244a0001c0002t0002g0248a0001c0002t0002g0340 | 3 | HG00099.hp1 HG00639.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.133-414T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869308 | |||||||
| chr11:77869312 | C | CT | 34 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0109others(31): Show | 36 | HG00597.hp2 HG00735.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.133-391dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77869312 | ||||||
| chr11:77869312 | C | CTT | 64 | a0001c0002t0001g0017a0001c0002t0001g0023a0001c0002t0001g0025others(61): Show | 67 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.133-392_133-391dup others(2): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77869312 | ||||||
| chr11:77869312 | C | T | 75 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0112others(72): Show | 77 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.133-410C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869312 | |||||||
| chr11:77869312 | CT | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0315a0001c0001t0001g0322others(4): Show | 7 | HG01167.hp1 HG01256.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-391delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77869312 | ||||||
| chr11:77869321 | T | C | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133-401T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869321 | |||||||
| chr11:77869449 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.133-273G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | 77869449 | |||||||
| chr11:77869502 | ACGGT | A | 155 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(152): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.133-214_133-211del others(4): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | 77869502 | ||||||
| chr11:77869949 | G | A | 155 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(152): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.228+132G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77869949 | |||||||
| chr11:77870185 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.228+368T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870185 | |||||||
| chr11:77870199 | A | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.228+382A>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870199 | |||||||
| chr11:77870329 | A | AT | 29 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0174others(26): Show | 29 | HG00423.hp2 HG01074.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.228+538dupT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 77870329 | ||||||
| chr11:77870329 | AT | A | 83 | a0001c0001t0001g0099a0001c0001t0001g0121a0001c0001t0001g0131others(80): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.228+538delT | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 77870329 | ||||||
| chr11:77870329 | ATT | A | 9 | a0001c0002t0001g0014a0001c0002t0001g0025a0001c0002t0001g0026others(6): Show | 9 | HG01109.hp2 HG01168.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.228+537_228+538del others(2): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | 77870329 | ||||||
| chr11:77870370 | T | A | 69 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074others(66): Show | 72 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.228+553T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870370 | |||||||
| chr11:77870376 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.228+559C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870376 | |||||||
| chr11:77870398 | G | A | 70 | a0001c0002t0001g0017a0001c0002t0001g0023a0001c0002t0001g0025others(67): Show | 73 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.228+581G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870398 | |||||||
| chr11:77870589 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.228+772A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870589 | |||||||
| chr11:77870598 | A | G | 69 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074others(66): Show | 72 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.228+781A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870598 | |||||||
| chr11:77870648 | T | G | 1 | a0001c0001t0001g0362 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.228+831T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870648 | |||||||
| chr11:77870665 | A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0210 | 2 | NA19003.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.228+848A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870665 | |||||||
| chr11:77870707 | T | G | 1 | a0001c0002t0002g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.228+890T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870707 | |||||||
| chr11:77870714 | A | G | 1 | a0001c0002t0002g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.228+897A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870714 | |||||||
| chr11:77870878 | T | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0184a0001c0001t0001g0190others(1): Show | 4 | NA18940.hp1 NA18988.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+1061T>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77870878 | |||||||
| chr11:77871145 | T | C | 1 | a0001c0002t0002g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.229-1030T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871145 | |||||||
| chr11:77871168 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.229-1007G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871168 | |||||||
| chr11:77871328 | A | G | 3 | a0001c0002t0001g0067a0001c0002t0001g0069a0001c0002t0001g0074 | 3 | HG01081.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.229-847A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871328 | |||||||
| chr11:77871478 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.229-697A>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871478 | |||||||
| chr11:77871511 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.229-664T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871511 | |||||||
| chr11:77871697 | C | T | 155 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0023others(152): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.229-478C>T | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871697 | |||||||
| chr11:77871802 | T | G | 1 | a0002c0003t0001g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.229-373T>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871802 | |||||||
| chr11:77871914 | T | C | 1 | a0001c0002t0002g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.229-261T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871914 | |||||||
| chr11:77871983 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.229-192G>A | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77871983 | |||||||
| chr11:77872002 | C | G | 6 | a0001c0002t0002g0112a0001c0002t0002g0205a0001c0002t0002g0342others(3): Show | 6 | HG01496.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.229-173C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77872002 | |||||||
| chr11:77872015 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.229-160T>C | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77872015 | |||||||
| chr11:77872089 | C | G | 2 | a0001c0002t0002g0266a0001c0002t0002g0267 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.229-86C>G | AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | 77872089 |