Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 50 |
| ensemblid | ENSG00000100412.17 |
| hgncid | 118 |
| symbol | ACO2 |
| name | aconitase 2 |
| refseq_nuc | NM_001098.3 |
| refseq_prot | NP_001089.1 |
| ensembl_nuc | ENST00000216254.9 |
| ensembl_prot | ENSP00000216254.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 41469117 |
| end | 41528974 |
| strand | + |
| ver | v1.2 |
| region | chr22:41469117-41528974 |
| region5000 | chr22:41464117-41533974 |
| regionname0 | ACO2_chr22_41469117_41528974 |
| regionname5000 | ACO2_chr22_41464117_41533974 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 780 | 331 | 89 | 58 | 138 | 12 | 32 | 100 | ACO2_chr22_41464117_41533974 | ACO2 | MAPYS others(775): Show |
chr22 | 41464117 | 41533974 |
| a0002 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | MAPYS others(775): Show |
chr22 | 41464117 | 41533974 |
| a0003 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | MAPYS others(775): Show |
chr22 | 41464117 | 41533974 |
| a0004 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | MAPYS others(775): Show |
chr22 | 41464117 | 41533974 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2340 | 146 | 30 | 29 | 69 | 3 | 15 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0001c0002 | 1/0 | 2340 | 90 | 39 | 12 | 28 | 3 | 7 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0001c0003 | 0/1 | 2340 | 85 | 11 | 17 | 40 | 6 | 10 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0001c0004 | 0/0 | 2340 | 4 | 4 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0001c0005 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0001c0006 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0001c0009 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0001c0010 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0002c0008 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0003c0007 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 | ||
| a0004c0011 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | ATGGC others(2335): Show |
chr22 | 41464117 | 41533974 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2734 | 142 | 27 | 29 | 68 | 3 | 15 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0001t0002 | 0/0 | 2734 | 3 | 3 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0001t0003 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0002t0001 | 1/0 | 2734 | 90 | 39 | 12 | 28 | 3 | 7 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0003t0001 | 0/1 | 2734 | 84 | 11 | 17 | 39 | 6 | 10 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0003t0004 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0004t0001 | 0/0 | 2734 | 4 | 4 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0005t0001 | 0/0 | 2734 | 2 | 2 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0006t0002 | 0/0 | 2734 | 2 | 2 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0009t0001 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0001c0010t0001 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0002c0008t0001 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0003c0007t0001 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| a0004c0011t0001 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | AATGC others(2729): Show |
chr22 | 41464117 | 41533974 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0003t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0006t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0006t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0009t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0001c0010t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0002c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0003c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| a0004c0011t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0062 | EUR | GBR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0093 | EUR | GBR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0015 | EUR | GBR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0131 | EUR | GBR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0292 | EUR | FIN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0091 | EUR | FIN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00408 | hp2 | a0001 | c0009 | t0001 | g0105 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0060 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0312 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0069 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0074 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0301 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0293 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0300 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0295 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0297 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0298 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0299 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0307 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | PUR | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0049 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0150 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0136 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0303 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0138 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0044 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0063 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02257 | hp2 | a0001 | c0006 | t0002 | g0155 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | PEL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0294 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0308 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0164 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0134 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0144 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0140 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0306 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03209 | hp1 | a0001 | c0006 | t0002 | g0152 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0015 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0073 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0054 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | BEB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0291 | SAS | BEB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0302 | SAS | BEB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | BEB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0087 | SAS | BEB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0085 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0290 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18522 | hp2 | a0002 | c0008 | t0001 | g0159 | AFR | YRI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | CHB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | CHB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | YRI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18946 | hp1 | a0003 | c0007 | t0001 | g0046 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18965 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18992 | hp1 | a0001 | c0003 | t0004 | g0203 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18995 | hp2 | a0004 | c0011 | t0001 | g0260 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | LWK | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | LWK | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0310 | AFR | LWK | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19076 | hp2 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0055 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | YRI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ASW | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ASW | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0296 | EUR | TSI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0041 | EUR | TSI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0075 | EUR | TSI | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG02559 | hp2 | a0001 | c0010 | t0001 | g0157 | AFR | ACB | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | USA | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | USA | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | USA | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | USA | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | LWK | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | LWK | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0132 | REF | REF | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0177 | REF | REF | ACO2_chr22_41464117_41533974 | ACO2 | chr22 | 41464117 | 41533974 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41507854 | C | A | 1 | a0003 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.237C>A | p.Ser79Arg | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/18 | 267/2734 | 237/2343 | 79/780 | chr22 | 41507854 | |||
| chr22:41523846 | G | T | 1 | a0004 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.1387G>T | p.Gly463Trp | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 12/18 | 1417/2734 | 1387/2343 | 463/780 | chr22 | 41523846 | |||
| chr22:41528548 | G | A | 1 | a0002 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.2278G>A | p.Glu760Lys | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 18/18 | 2308/2734 | 2278/2343 | 760/780 | chr22 | 41528548 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41499773 | A | G | 1 | a0001c0006 | 2 | HG02257.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.84A>G | p.Gln28Gln | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/18 | 114/2734 | 84/2343 | 28/780 | chr22 | 41499773 | |||
| chr22:41507809 | A | C | 5 | a0001c0001 a0001c0004 a0001c0006 others(2): Show |
154 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
synonymous_variant | LOW | c.192A>C | p.Thr64Thr | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/18 | 222/2734 | 192/2343 | 64/780 | chr22 | 41507809 | |||
| chr22:41511929 | C | T | 1 | a0001c0004 | 4 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.486C>T | p.Gly162Gly | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/18 | 516/2734 | 486/2343 | 162/780 | chr22 | 41511929 | |||
| chr22:41515521 | C | T | 2 | a0001c0003 a0003c0007 |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
synonymous_variant | LOW | c.670C>T | p.Leu224Leu | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 5/18 | 700/2734 | 670/2343 | 224/780 | chr22 | 41515521 | |||
| chr22:41520176 | G | A | 1 | a0001c0010 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1038G>A | p.Lys346Lys | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/18 | 1068/2734 | 1038/2343 | 346/780 | chr22 | 41520176 | |||
| chr22:41527314 | C | T | 1 | a0001c0005 | 2 | HG01884.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.1980C>T | p.Ile660Ile | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 16/18 | 2010/2734 | 1980/2343 | 660/780 | chr22 | 41527314 | |||
| chr22:41528553 | G | A | 1 | a0001c0009 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.2283G>A | p.Thr761Thr | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 18/18 | 2313/2734 | 2283/2343 | 761/780 | chr22 | 41528553 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41528616 | G | A | 1 | a0001c0001t0003 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 18/18 | 3 | chr22 | 41528616 | ||||||
| chr22:41528774 | G | T | 2 | a0001c0001t0002 a0001c0006t0002 |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 18/18 | 161 | chr22 | 41528774 | ||||||
| chr22:41528879 | C | T | 1 | a0001c0003t0004 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 18/18 | 266 | chr22 | 41528879 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41469330 | G | A | 1 | a0001c0002t0001g0005 | 2 | HG01106.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.36+148G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41469330 | |||||||
| chr22:41469645 | C | T | 10 | a0001c0001t0001g0309 a0001c0002t0001g0303 a0001c0002t0001g0304 others(7): Show |
10 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.36+463C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41469645 | |||||||
| chr22:41469705 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.36+523G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41469705 | |||||||
| chr22:41469735 | A | G | 14 | a0001c0003t0001g0015 a0001c0003t0001g0290 a0001c0003t0001g0291 others(11): Show |
15 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.36+553A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41469735 | |||||||
| chr22:41469788 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0214 a0001c0001t0001g0215 others(75): Show |
83 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.36+606A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41469788 | |||||||
| chr22:41469805 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(235): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.36+623C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41469805 | |||||||
| chr22:41469839 | TGATA | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(235): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.36+661_36+664delAG others(2): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41469839 | ||||||
| chr22:41469853 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.36+671G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41469853 | |||||||
| chr22:41470151 | G | T | 1 | a0001c0001t0001g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.36+969G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41470151 | |||||||
| chr22:41470528 | C | CT | 23 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(20): Show |
23 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.36+1380dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41470528 | ||||||
| chr22:41470528 | C | CTT | 10 | a0001c0001t0001g0013 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
11 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.36+1379_36+1380dup others(2): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41470528 | ||||||
| chr22:41470528 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0156 a0001c0001t0002g0151 a0001c0001t0002g0153 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.36+1373_36+1380del others(8): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41470528 | ||||||
| chr22:41470528 | CTTTTTTT others(7): Show |
C | 9 | a0001c0002t0001g0145 a0001c0003t0001g0137 a0001c0003t0001g0141 others(6): Show |
9 | HG01891.hp2 HG02148.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.36+1367_36+1380del others(14): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41470528 | ||||||
| chr22:41470528 | CTTTTTTT others(8): Show |
C | 158 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0001g0082 others(155): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.36+1366_36+1380del others(15): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41470528 | ||||||
| chr22:41470528 | CTTTTTTT others(9): Show |
C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(72): Show |
80 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.36+1365_36+1380del others(16): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41470528 | ||||||
| chr22:41470682 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+1500A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41470682 | |||||||
| chr22:41470761 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.36+1579A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41470761 | |||||||
| chr22:41470889 | T | C | 2 | a0001c0001t0001g0158 a0001c0010t0001g0157 |
2 | HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.36+1707T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41470889 | |||||||
| chr22:41470934 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(236): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.36+1752A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41470934 | |||||||
| chr22:41470999 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.36+1817C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41470999 | |||||||
| chr22:41471101 | T | TTGTC | 239 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(236): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.36+1920_36+1923dup others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41471101 | ||||||
| chr22:41471261 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+2079C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41471261 | |||||||
| chr22:41471292 | T | G | 1 | a0001c0003t0001g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.36+2110T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41471292 | |||||||
| chr22:41471368 | A | C | 4 | a0001c0003t0001g0133 a0001c0003t0001g0134 a0001c0003t0001g0135 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2186A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41471368 | |||||||
| chr22:41471373 | C | T | 129 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0001g0124 others(126): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.36+2191C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41471373 | |||||||
| chr22:41471516 | A | G | 1 | a0001c0002t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.36+2334A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41471516 | |||||||
| chr22:41471533 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.36+2351A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41471533 | |||||||
| chr22:41471904 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+2722C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41471904 | |||||||
| chr22:41472108 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.36+2926A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41472108 | |||||||
| chr22:41472137 | A | G | 2 | a0001c0002t0001g0129 a0001c0002t0001g0130 |
2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.36+2955A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41472137 | |||||||
| chr22:41472179 | C | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
7 | NA18969.hp1 NA18975.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+2997C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41472179 | |||||||
| chr22:41472352 | C | CA | 22 | a0001c0001t0001g0199 a0001c0001t0001g0214 a0001c0001t0001g0215 others(19): Show |
22 | HG01891.hp1 HG02080.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.36+3188dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41472352 | ||||||
| chr22:41472352 | CA | C | 8 | a0001c0001t0001g0278 a0001c0001t0001g0288 a0001c0002t0001g0126 others(5): Show |
8 | HG01257.hp1 HG01884.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.36+3188delA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41472352 | ||||||
| chr22:41472570 | T | C | 1 | a0001c0002t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.36+3388T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41472570 | |||||||
| chr22:41472690 | A | G | 16 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.36+3508A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41472690 | |||||||
| chr22:41472727 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.36+3545C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41472727 | |||||||
| chr22:41472766 | A | G | 2 | a0001c0001t0001g0158 a0001c0010t0001g0157 |
2 | HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.36+3584A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41472766 | |||||||
| chr22:41473264 | G | T | 46 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0005 others(43): Show |
53 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.36+4082G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41473264 | |||||||
| chr22:41473621 | T | C | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.36+4439T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41473621 | |||||||
| chr22:41473827 | C | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
7 | NA18969.hp1 NA18975.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+4645C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41473827 | |||||||
| chr22:41473897 | C | T | 2 | a0001c0001t0001g0158 a0001c0010t0001g0157 |
2 | HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.36+4715C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41473897 | |||||||
| chr22:41473989 | G | T | 1 | a0001c0003t0001g0302 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.36+4807G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41473989 | |||||||
| chr22:41474016 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.36+4834G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474016 | |||||||
| chr22:41474161 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.36+4979A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474161 | |||||||
| chr22:41474197 | G | C | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+5015G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474197 | |||||||
| chr22:41474229 | G | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0204 others(1): Show |
4 | HG01192.hp1 HG02451.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+5047G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474229 | |||||||
| chr22:41474274 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.36+5092C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474274 | |||||||
| chr22:41474289 | A | AT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(93): Show |
101 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.36+5129dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474289 | ||||||
| chr22:41474289 | A | ATT | 10 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0219 others(7): Show |
10 | HG02145.hp2 NA18981.hp1 NA18985.hp1 others(7): Show |
intron_variant | MODIFIER | c.36+5128_36+5129dup others(2): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474289 | ||||||
| chr22:41474289 | AT | A | 10 | a0001c0001t0001g0158 a0001c0002t0001g0007 a0001c0002t0001g0033 others(7): Show |
11 | HG00323.hp2 HG01099.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+5129delT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474289 | ||||||
| chr22:41474289 | ATT | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(15): Show |
18 | HG01884.hp1 HG01934.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.36+5128_36+5129del others(2): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474289 | ||||||
| chr22:41474357 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01109.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.36+5175G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474357 | |||||||
| chr22:41474362 | CGGCTCAC others(298): Show |
C | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+5197_36+5501del | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474362 | ||||||
| chr22:41474369 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.36+5187C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474369 | |||||||
| chr22:41474447 | C | T | 1 | a0001c0003t0001g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.36+5265C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474447 | |||||||
| chr22:41474485 | C | T | 1 | a0001c0002t0001g0086 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.36+5303C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474485 | |||||||
| chr22:41474592 | C | CT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0198 a0001c0001t0001g0286 others(5): Show |
8 | HG02647.hp1 HG03139.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+5434dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474592 | ||||||
| chr22:41474592 | CT | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(206): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.36+5434delT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474592 | ||||||
| chr22:41474592 | CTTT | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0158 a0001c0001t0001g0165 others(8): Show |
11 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+5432_36+5434del others(3): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474592 | ||||||
| chr22:41474592 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0249 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.36+5423_36+5434del others(12): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41474592 | ||||||
| chr22:41474622 | G | A | 2 | a0001c0002t0001g0042 a0001c0002t0001g0086 |
2 | NA18955.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.36+5440G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474622 | |||||||
| chr22:41474669 | G | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+5487G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474669 | |||||||
| chr22:41474744 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(44): Show |
51 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.36+5562G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474744 | |||||||
| chr22:41474810 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(106): Show |
114 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.36+5628G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474810 | |||||||
| chr22:41474916 | A | G | 4 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0006t0002g0152 others(1): Show |
4 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+5734A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474916 | |||||||
| chr22:41474948 | T | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0265 a0001c0001t0001g0284 |
3 | HG00673.hp1 NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.36+5766T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41474948 | |||||||
| chr22:41475012 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+5830G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475012 | |||||||
| chr22:41475071 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+5889C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475071 | |||||||
| chr22:41475145 | T | TA | 23 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(20): Show |
23 | HG00099.hp2 HG00642.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.36+5976dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41475145 | ||||||
| chr22:41475169 | C | CT | 25 | a0001c0001t0001g0016 a0001c0001t0001g0181 a0001c0001t0001g0191 others(22): Show |
25 | HG00642.hp2 HG01884.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.36+6008dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41475169 | ||||||
| chr22:41475169 | CT | C | 16 | a0001c0001t0001g0165 a0001c0001t0001g0169 a0001c0001t0001g0179 others(13): Show |
16 | HG01884.hp1 HG02148.hp2 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.36+6008delT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41475169 | ||||||
| chr22:41475191 | G | C | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.36+6009G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475191 | |||||||
| chr22:41475318 | A | G | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+6136A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475318 | |||||||
| chr22:41475459 | G | A | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0193 others(2): Show |
5 | HG01175.hp1 HG01192.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+6277G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475459 | |||||||
| chr22:41475534 | G | T | 1 | a0001c0003t0001g0302 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.36+6352G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475534 | |||||||
| chr22:41475621 | G | A | 1 | a0001c0002t0001g0121 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.36+6439G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475621 | |||||||
| chr22:41475665 | T | C | 20 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0158 others(17): Show |
20 | HG01099.hp2 HG01884.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.36+6483T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475665 | |||||||
| chr22:41475744 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0211 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.36+6562A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475744 | |||||||
| chr22:41475837 | G | C | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+6655G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41475837 | |||||||
| chr22:41475897 | C | CA | 62 | a0001c0001t0001g0158 a0001c0001t0001g0193 a0001c0001t0001g0199 others(59): Show |
69 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.36+6731dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41475897 | ||||||
| chr22:41476115 | A | G | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+6933A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41476115 | |||||||
| chr22:41476185 | A | T | 9 | a0001c0001t0001g0309 a0001c0002t0001g0303 a0001c0002t0001g0304 others(6): Show |
9 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.36+7003A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41476185 | |||||||
| chr22:41476220 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(44): Show |
51 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.36+7038C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41476220 | |||||||
| chr22:41476260 | AGTC | A | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+7079_36+7081del others(3): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41476260 | |||||||
| chr22:41476321 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.36+7139C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41476321 | |||||||
| chr22:41476407 | T | TA | 28 | a0001c0001t0001g0016 a0001c0001t0001g0158 a0001c0001t0001g0165 others(25): Show |
28 | HG01099.hp2 HG01934.hp2 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.36+7243dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41476407 | ||||||
| chr22:41476696 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.36+7514C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41476696 | |||||||
| chr22:41477073 | C | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+7891C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477073 | |||||||
| chr22:41477116 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.36+7934G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477116 | |||||||
| chr22:41477128 | TATTA | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0264 a0001c0001t0001g0278 |
3 | NA18961.hp2 NA18994.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.36+7947_36+7950del others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477128 | |||||||
| chr22:41477129 | A | ATTAT | 12 | a0001c0001t0001g0146 a0001c0001t0001g0204 a0001c0001t0001g0269 others(9): Show |
12 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.36+7982_36+7985dup others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41477129 | ||||||
| chr22:41477129 | A | ATTATTTA others(5): Show |
1 | a0001c0002t0001g0095 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.36+7974_36+7985dup others(12): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41477129 | ||||||
| chr22:41477129 | ATTAT | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0165 a0001c0002t0001g0033 others(11): Show |
14 | HG01884.hp1 HG01934.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.36+7982_36+7985del others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41477129 | ||||||
| chr22:41477129 | ATTATTTA others(1): Show |
A | 25 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0309 others(22): Show |
27 | HG00639.hp2 HG01099.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.36+7978_36+7985del others(8): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41477129 | ||||||
| chr22:41477160 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+7978A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477160 | |||||||
| chr22:41477164 | A | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0249 |
2 | HG02080.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.36+7982A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477164 | |||||||
| chr22:41477189 | T | C | 3 | a0001c0002t0001g0094 a0001c0002t0001g0095 a0001c0002t0001g0096 |
3 | NA18961.hp1 NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.36+8007T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477189 | |||||||
| chr22:41477215 | G | A | 2 | a0001c0003t0001g0133 a0001c0003t0001g0136 |
2 | HG01884.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.36+8033G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477215 | |||||||
| chr22:41477239 | C | T | 1 | a0001c0003t0001g0079 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.36+8057C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477239 | |||||||
| chr22:41477373 | A | G | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+8191A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477373 | |||||||
| chr22:41477411 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
5 | HG02280.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+8229G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477411 | |||||||
| chr22:41477706 | C | T | 2 | a0001c0002t0001g0129 a0001c0002t0001g0130 |
2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.36+8524C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477706 | |||||||
| chr22:41477908 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+8726T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41477908 | |||||||
| chr22:41478258 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0010t0001g0157 |
3 | HG01099.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.36+9076C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478258 | |||||||
| chr22:41478349 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.36+9167G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478349 | |||||||
| chr22:41478462 | C | G | 2 | a0001c0001t0001g0158 a0001c0010t0001g0157 |
2 | HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.36+9280C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478462 | |||||||
| chr22:41478716 | T | G | 1 | a0001c0003t0001g0044 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.36+9534T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478716 | |||||||
| chr22:41478736 | C | T | 8 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0002g0151 others(5): Show |
8 | HG01099.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+9554C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478736 | |||||||
| chr22:41478764 | C | CT | 19 | a0001c0001t0001g0199 a0001c0001t0001g0247 a0001c0001t0001g0248 others(16): Show |
19 | HG01069.hp1 HG01243.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.36+9602dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41478764 | ||||||
| chr22:41478764 | CT | C | 21 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0170 others(18): Show |
21 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.36+9602delT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41478764 | ||||||
| chr22:41478767 | T | C | 3 | a0001c0002t0001g0166 a0001c0002t0001g0167 a0002c0008t0001g0159 |
3 | HG02886.hp1 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.36+9585T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478767 | |||||||
| chr22:41478783 | T | C | 16 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(13): Show |
16 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.36+9601T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478783 | |||||||
| chr22:41478848 | G | A | 1 | a0001c0003t0001g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.36+9666G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478848 | |||||||
| chr22:41478962 | A | G | 2 | a0001c0003t0001g0026 a0001c0003t0001g0027 |
2 | NA18940.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.36+9780A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41478962 | |||||||
| chr22:41479157 | G | T | 1 | a0001c0002t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.36+9975G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479157 | |||||||
| chr22:41479158 | G | T | 1 | a0001c0003t0001g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.36+9976G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479158 | |||||||
| chr22:41479235 | G | A | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.36+10053G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479235 | |||||||
| chr22:41479251 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+10069A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479251 | |||||||
| chr22:41479290 | A | G | 2 | a0001c0001t0001g0158 a0001c0010t0001g0157 |
2 | HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.36+10108A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479290 | |||||||
| chr22:41479377 | A | C | 16 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0002g0151 others(13): Show |
16 | HG01099.hp2 HG01243.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.36+10195A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479377 | |||||||
| chr22:41479766 | C | T | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.36+10584C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479766 | |||||||
| chr22:41479800 | T | C | 58 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0002t0001g0042 others(55): Show |
61 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.36+10618T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479800 | |||||||
| chr22:41479896 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.36+10714C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479896 | |||||||
| chr22:41479918 | C | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02451.hp1 HG06807.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.36+10736C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41479918 | |||||||
| chr22:41480201 | C | T | 1 | a0001c0002t0001g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.36+11019C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41480201 | |||||||
| chr22:41480530 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.36+11348C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41480530 | |||||||
| chr22:41480593 | C | A | 12 | a0001c0001t0001g0089 a0001c0001t0001g0156 a0001c0001t0001g0289 others(9): Show |
13 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+11411C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41480593 | |||||||
| chr22:41480671 | A | T | 7 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+11489A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41480671 | |||||||
| chr22:41480918 | C | G | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+11736C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41480918 | |||||||
| chr22:41480951 | G | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01109.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.36+11769G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41480951 | |||||||
| chr22:41480955 | A | G | 1 | a0001c0003t0001g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.36+11773A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41480955 | |||||||
| chr22:41481013 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.36+11831T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481013 | |||||||
| chr22:41481107 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.36+11925C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481107 | |||||||
| chr22:41481330 | A | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+12148A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481330 | |||||||
| chr22:41481526 | A | G | 3 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0197 |
3 | HG01346.hp2 HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.36+12344A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481526 | |||||||
| chr22:41481572 | C | T | 2 | a0001c0002t0001g0166 a0001c0002t0001g0167 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.36+12390C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481572 | |||||||
| chr22:41481573 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.36+12391G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481573 | |||||||
| chr22:41481715 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.36+12533C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481715 | |||||||
| chr22:41481768 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(44): Show |
51 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.36+12586G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481768 | |||||||
| chr22:41481985 | A | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(259): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.36+12803A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41481985 | |||||||
| chr22:41482045 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.36+12863T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482045 | |||||||
| chr22:41482068 | G | A | 1 | a0001c0002t0001g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.36+12886G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482068 | |||||||
| chr22:41482330 | G | C | 1 | a0001c0003t0001g0049 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.36+13148G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482330 | |||||||
| chr22:41482363 | T | C | 1 | a0001c0002t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.36+13181T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482363 | |||||||
| chr22:41482482 | G | T | 7 | a0001c0001t0001g0156 a0001c0001t0002g0151 a0001c0001t0002g0153 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.36+13300G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482482 | |||||||
| chr22:41482591 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(77): Show |
85 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.36+13409C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482591 | |||||||
| chr22:41482730 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.36+13548C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482730 | |||||||
| chr22:41482873 | G | C | 1 | a0001c0003t0001g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.36+13691G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482873 | |||||||
| chr22:41482997 | C | A | 1 | a0001c0001t0001g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.36+13815C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41482997 | |||||||
| chr22:41483287 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.36+14105C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41483287 | |||||||
| chr22:41483432 | G | A | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.36+14250G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41483432 | |||||||
| chr22:41483924 | A | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0165 a0001c0002t0001g0014 others(15): Show |
19 | HG01884.hp1 HG01934.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.36+14742A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41483924 | |||||||
| chr22:41484008 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.36+14826C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41484008 | |||||||
| chr22:41484046 | G | C | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.36+14864G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41484046 | |||||||
| chr22:41484701 | A | G | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-15025A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41484701 | |||||||
| chr22:41484766 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(111): Show |
119 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.37-14960A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41484766 | |||||||
| chr22:41484871 | C | CT | 15 | a0001c0001t0001g0089 a0001c0001t0001g0178 a0001c0001t0001g0199 others(12): Show |
15 | HG02027.hp1 HG02132.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-14835dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41484871 | ||||||
| chr22:41484898 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.37-14828G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41484898 | |||||||
| chr22:41484936 | G | A | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-14790G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41484936 | |||||||
| chr22:41485082 | G | A | 1 | a0001c0003t0001g0050 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.37-14644G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485082 | |||||||
| chr22:41485106 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.37-14620A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485106 | |||||||
| chr22:41485124 | A | G | 28 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(25): Show |
29 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.37-14602A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485124 | |||||||
| chr22:41485163 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01109.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.37-14563C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485163 | |||||||
| chr22:41485165 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0276 |
2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.37-14561C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485165 | |||||||
| chr22:41485167 | T | C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(25): Show |
29 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.37-14559T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485167 | |||||||
| chr22:41485416 | C | T | 1 | a0001c0002t0001g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.37-14310C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485416 | |||||||
| chr22:41485426 | C | G | 1 | a0001c0001t0002g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.37-14300C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485426 | |||||||
| chr22:41485434 | A | AT | 6 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0196 others(3): Show |
6 | HG00423.hp1 HG01099.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-14268dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41485434 | ||||||
| chr22:41485434 | AT | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(219): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.37-14268delT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41485434 | ||||||
| chr22:41485434 | ATT | A | 12 | a0001c0001t0001g0221 a0001c0001t0001g0283 a0001c0001t0002g0151 others(9): Show |
13 | HG01069.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.37-14269_37-14268d others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41485434 | ||||||
| chr22:41485471 | C | T | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-14255C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485471 | |||||||
| chr22:41485475 | C | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(44): Show |
51 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.37-14251C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485475 | |||||||
| chr22:41485541 | C | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-14185C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485541 | |||||||
| chr22:41485590 | A | G | 28 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(25): Show |
29 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.37-14136A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485590 | |||||||
| chr22:41485592 | C | G | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-14134C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485592 | |||||||
| chr22:41485598 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0168 a0001c0001t0001g0171 others(2): Show |
6 | HG00323.hp1 HG00733.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-14128G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485598 | |||||||
| chr22:41485665 | G | T | 3 | a0001c0001t0001g0224 a0001c0001t0001g0282 a0001c0001t0001g0286 |
3 | NA18945.hp1 NA18947.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.37-14061G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485665 | |||||||
| chr22:41485689 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37-14037C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485689 | |||||||
| chr22:41485690 | G | A | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-14036G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485690 | |||||||
| chr22:41485730 | A | G | 1 | a0001c0002t0001g0117 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.37-13996A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485730 | |||||||
| chr22:41485743 | C | T | 8 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(5): Show |
8 | HG02257.hp2 HG02886.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-13983C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41485743 | |||||||
| chr22:41486042 | G | C | 14 | a0001c0001t0001g0165 a0001c0002t0001g0160 a0001c0002t0001g0161 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37-13684G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41486042 | |||||||
| chr22:41486324 | C | T | 3 | a0001c0002t0001g0007 a0001c0002t0001g0034 a0001c0002t0001g0035 |
4 | HG02280.hp2 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-13402C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41486324 | |||||||
| chr22:41486325 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.37-13401G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41486325 | |||||||
| chr22:41486397 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.37-13329G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41486397 | |||||||
| chr22:41486455 | G | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0165 a0001c0002t0001g0014 others(13): Show |
17 | HG01884.hp1 HG01934.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-13271G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41486455 | |||||||
| chr22:41486469 | A | AT | 13 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG00735.hp1 HG00741.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.37-13238dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41486469 | ||||||
| chr22:41486469 | A | ATT | 17 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(14): Show |
18 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.37-13239_37-13238d others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41486469 | ||||||
| chr22:41486469 | A | ATTT | 8 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(5): Show |
8 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-13240_37-13238d others(5): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41486469 | ||||||
| chr22:41486534 | G | A | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.37-13192G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41486534 | |||||||
| chr22:41486608 | G | T | 1 | a0001c0002t0001g0310 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.37-13118G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41486608 | |||||||
| chr22:41487030 | C | T | 5 | a0001c0003t0001g0036 a0001c0003t0001g0043 a0001c0003t0001g0047 others(2): Show |
5 | NA18962.hp1 NA18963.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-12696C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41487030 | |||||||
| chr22:41487050 | A | G | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.37-12676A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41487050 | |||||||
| chr22:41487427 | A | C | 4 | a0001c0003t0001g0133 a0001c0003t0001g0134 a0001c0003t0001g0135 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-12299A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41487427 | |||||||
| chr22:41487582 | C | A | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.37-12144C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41487582 | |||||||
| chr22:41487790 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(75): Show |
82 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.37-11936A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41487790 | |||||||
| chr22:41487821 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.37-11905G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41487821 | |||||||
| chr22:41488006 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.37-11720G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41488006 | |||||||
| chr22:41488180 | C | T | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.37-11546C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41488180 | |||||||
| chr22:41488710 | C | G | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-11016C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41488710 | |||||||
| chr22:41488950 | A | G | 20 | a0001c0001t0001g0124 a0001c0003t0001g0015 a0001c0003t0001g0044 others(17): Show |
21 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.37-10776A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41488950 | |||||||
| chr22:41489203 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.37-10523C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489203 | |||||||
| chr22:41489336 | G | T | 1 | a0001c0001t0001g0245 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.37-10390G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489336 | |||||||
| chr22:41489338 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.37-10388A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489338 | |||||||
| chr22:41489450 | C | A | 1 | a0001c0002t0001g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37-10276C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489450 | |||||||
| chr22:41489748 | C | T | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.37-9978C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489748 | |||||||
| chr22:41489835 | A | G | 1 | a0001c0003t0001g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.37-9891A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489835 | |||||||
| chr22:41489915 | G | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01109.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.37-9811G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489915 | |||||||
| chr22:41489941 | A | G | 26 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(23): Show |
27 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-9785A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489941 | |||||||
| chr22:41489961 | C | G | 2 | a0001c0002t0001g0109 a0001c0002t0001g0113 |
2 | HG01346.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.37-9765C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489961 | |||||||
| chr22:41489974 | C | G | 5 | a0001c0002t0001g0007 a0001c0002t0001g0033 a0001c0002t0001g0034 others(2): Show |
6 | HG02280.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-9752C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41489974 | |||||||
| chr22:41490184 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.37-9542G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41490184 | |||||||
| chr22:41490219 | G | C | 2 | a0001c0001t0001g0156 a0001c0010t0001g0157 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.37-9507G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41490219 | |||||||
| chr22:41490389 | A | G | 1 | a0001c0002t0001g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37-9337A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41490389 | |||||||
| chr22:41490721 | G | A | 1 | a0001c0004t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.37-9005G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41490721 | |||||||
| chr22:41490899 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.37-8827C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41490899 | |||||||
| chr22:41491112 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG03195.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.37-8614C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41491112 | |||||||
| chr22:41491321 | G | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(75): Show |
82 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.37-8405G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41491321 | |||||||
| chr22:41491554 | A | G | 1 | a0001c0002t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.37-8172A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41491554 | |||||||
| chr22:41491820 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.37-7906G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41491820 | |||||||
| chr22:41491862 | G | T | 3 | a0001c0003t0001g0297 a0001c0003t0001g0298 a0001c0003t0001g0299 |
3 | HG01081.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.37-7864G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41491862 | |||||||
| chr22:41491918 | T | G | 28 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(25): Show |
29 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.37-7808T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41491918 | |||||||
| chr22:41491936 | A | G | 1 | a0001c0003t0001g0025 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.37-7790A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41491936 | |||||||
| chr22:41491972 | T | C | 1 | a0001c0003t0001g0085 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.37-7754T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41491972 | |||||||
| chr22:41492068 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37-7658T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41492068 | |||||||
| chr22:41492118 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37-7608C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41492118 | |||||||
| chr22:41492411 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01109.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.37-7315C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41492411 | |||||||
| chr22:41492466 | G | A | 1 | a0001c0004t0001g0139 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.37-7260G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41492466 | |||||||
| chr22:41492578 | A | G | 1 | a0001c0003t0001g0071 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.37-7148A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41492578 | |||||||
| chr22:41492602 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.37-7124C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41492602 | |||||||
| chr22:41493182 | G | GCCCTTCT others(3): Show |
1 | a0001c0003t0001g0080 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.37-6542_37-6533dup others(10): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41493182 | ||||||
| chr22:41493340 | A | C | 26 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(23): Show |
27 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-6386A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41493340 | |||||||
| chr22:41493359 | A | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(258): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.37-6367A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41493359 | |||||||
| chr22:41493398 | C | T | 16 | a0001c0001t0001g0016 a0001c0001t0001g0165 a0001c0002t0001g0014 others(13): Show |
17 | HG01884.hp1 HG01934.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-6328C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41493398 | |||||||
| chr22:41493645 | G | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(20): Show |
24 | HG01884.hp1 HG01934.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.37-6081G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41493645 | |||||||
| chr22:41493784 | C | T | 1 | a0001c0005t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.37-5942C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41493784 | |||||||
| chr22:41493787 | G | A | 3 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0144 |
3 | HG02886.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.37-5939G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41493787 | |||||||
| chr22:41493884 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.37-5842C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41493884 | |||||||
| chr22:41493964 | CAGG | C | 6 | a0001c0002t0001g0007 a0001c0002t0001g0033 a0001c0002t0001g0034 others(3): Show |
7 | HG02280.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-5759_37-5757del others(3): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41493964 | ||||||
| chr22:41494022 | C | A | 1 | a0001c0002t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.37-5704C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494022 | |||||||
| chr22:41494083 | G | A | 6 | a0001c0002t0001g0007 a0001c0002t0001g0033 a0001c0002t0001g0034 others(3): Show |
7 | HG02280.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-5643G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494083 | |||||||
| chr22:41494084 | G | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(20): Show |
24 | HG01884.hp1 HG01934.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.37-5642G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494084 | |||||||
| chr22:41494195 | C | T | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.37-5531C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494195 | |||||||
| chr22:41494206 | G | A | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-5520G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494206 | |||||||
| chr22:41494385 | C | A | 1 | a0001c0004t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.37-5341C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494385 | |||||||
| chr22:41494411 | C | CT | 12 | a0001c0001t0001g0156 a0001c0001t0001g0192 a0001c0001t0001g0220 others(9): Show |
12 | HG00673.hp1 HG00673.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-5298dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41494411 | ||||||
| chr22:41494411 | CT | C | 19 | a0001c0001t0001g0016 a0001c0001t0001g0165 a0001c0001t0001g0183 others(16): Show |
20 | HG01192.hp1 HG01884.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.37-5298delT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41494411 | ||||||
| chr22:41494441 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37-5285C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494441 | |||||||
| chr22:41494556 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.37-5170C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494556 | |||||||
| chr22:41494561 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.37-5165G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494561 | |||||||
| chr22:41494691 | G | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0165 a0001c0002t0001g0014 others(13): Show |
17 | HG01884.hp1 HG01934.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-5035G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494691 | |||||||
| chr22:41494885 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37-4841C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494885 | |||||||
| chr22:41494980 | C | T | 3 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0144 |
3 | HG02886.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.37-4746C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41494980 | |||||||
| chr22:41495368 | G | C | 2 | a0001c0002t0001g0160 a0001c0002t0001g0161 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.37-4358G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495368 | |||||||
| chr22:41495626 | C | CT | 248 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(245): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.37-4088dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 41495626 | ||||||
| chr22:41495676 | A | C | 1 | a0001c0002t0001g0115 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.37-4050A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495676 | |||||||
| chr22:41495765 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.37-3961C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495765 | |||||||
| chr22:41495778 | G | A | 1 | a0001c0003t0001g0080 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.37-3948G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495778 | |||||||
| chr22:41495781 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.37-3945G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495781 | |||||||
| chr22:41495834 | C | T | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-3892C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495834 | |||||||
| chr22:41495870 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37-3856G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495870 | |||||||
| chr22:41495880 | C | T | 1 | a0001c0003t0001g0071 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.37-3846C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495880 | |||||||
| chr22:41495969 | T | A | 1 | a0001c0003t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.37-3757T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41495969 | |||||||
| chr22:41496123 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0281 |
2 | HG02080.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.37-3603G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496123 | |||||||
| chr22:41496257 | G | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-3469G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496257 | |||||||
| chr22:41496604 | C | T | 6 | a0001c0001t0001g0165 a0001c0002t0001g0160 a0001c0002t0001g0161 others(3): Show |
6 | HG02451.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-3122C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496604 | |||||||
| chr22:41496614 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37-3112G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496614 | |||||||
| chr22:41496689 | A | G | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.37-3037A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496689 | |||||||
| chr22:41496736 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37-2990C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496736 | |||||||
| chr22:41496737 | A | G | 25 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0165 others(22): Show |
26 | HG01884.hp1 HG01934.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.37-2989A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496737 | |||||||
| chr22:41496832 | C | T | 2 | a0001c0002t0001g0116 a0001c0002t0001g0131 |
2 | HG00140.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.37-2894C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496832 | |||||||
| chr22:41496904 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.37-2822G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496904 | |||||||
| chr22:41496960 | G | A | 2 | a0001c0003t0001g0022 a0001c0003t0001g0023 |
2 | NA18977.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.37-2766G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41496960 | |||||||
| chr22:41497377 | T | TGGTTCAC others(5): Show |
5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-2349_37-2348ins others(12): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497377 | |||||||
| chr22:41497378 | C | A | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-2348C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497378 | |||||||
| chr22:41497395 | T | C | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-2331T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497395 | |||||||
| chr22:41497604 | T | G | 1 | a0001c0005t0001g0164 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.37-2122T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497604 | |||||||
| chr22:41497648 | C | T | 2 | a0001c0003t0001g0295 a0001c0003t0001g0296 |
2 | HG01070.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.37-2078C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497648 | |||||||
| chr22:41497649 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37-2077G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497649 | |||||||
| chr22:41497649 | G | T | 3 | a0001c0003t0001g0070 a0001c0003t0001g0071 a0003c0007t0001g0046 |
3 | NA18946.hp1 NA18979.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.37-2077G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497649 | |||||||
| chr22:41497685 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01109.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.37-2041C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497685 | |||||||
| chr22:41497912 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.37-1814G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497912 | |||||||
| chr22:41497942 | G | A | 1 | a0001c0003t0001g0041 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.37-1784G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41497942 | |||||||
| chr22:41498036 | C | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0069 a0001c0003t0001g0085 others(1): Show |
4 | HG00642.hp1 HG03831.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-1690C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41498036 | |||||||
| chr22:41498307 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0265 |
2 | NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.37-1419A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41498307 | |||||||
| chr22:41498334 | T | C | 10 | a0001c0001t0001g0192 a0001c0001t0001g0216 a0001c0001t0001g0220 others(7): Show |
10 | HG00673.hp1 HG01109.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.37-1392T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41498334 | |||||||
| chr22:41498343 | C | T | 1 | a0001c0002t0001g0108 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.37-1383C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41498343 | |||||||
| chr22:41498369 | T | C | 1 | a0001c0002t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.37-1357T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41498369 | |||||||
| chr22:41498612 | G | A | 1 | a0001c0003t0001g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.37-1114G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41498612 | |||||||
| chr22:41498836 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.37-890G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41498836 | |||||||
| chr22:41499048 | G | A | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-678G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41499048 | |||||||
| chr22:41499050 | T | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(306): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.37-676T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41499050 | |||||||
| chr22:41499405 | G | A | 51 | a0001c0001t0001g0045 a0001c0003t0001g0003 a0001c0003t0001g0008 others(48): Show |
54 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.37-321G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41499405 | |||||||
| chr22:41499682 | C | T | 3 | a0001c0003t0001g0297 a0001c0003t0001g0298 a0001c0003t0001g0299 |
3 | HG01081.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.37-44C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 1/17 | chr22 | 41499682 | |||||||
| chr22:41499904 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.173+42C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41499904 | |||||||
| chr22:41499919 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.173+57C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41499919 | |||||||
| chr22:41499925 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.173+63G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41499925 | |||||||
| chr22:41500010 | A | G | 1 | a0001c0002t0001g0107 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.173+148A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500010 | |||||||
| chr22:41500294 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.173+432T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500294 | |||||||
| chr22:41500300 | A | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0211 a0001c0003t0001g0079 |
3 | HG01070.hp2 HG01192.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.173+438A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500300 | |||||||
| chr22:41500305 | T | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(105): Show |
116 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.173+443T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500305 | |||||||
| chr22:41500310 | T | A | 21 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0001g0224 others(18): Show |
21 | HG02040.hp2 HG02056.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.173+448T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500310 | |||||||
| chr22:41500380 | T | A | 1 | a0001c0001t0001g0236 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.173+518T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500380 | |||||||
| chr22:41500415 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.173+553C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500415 | |||||||
| chr22:41500449 | A | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0165 a0001c0002t0001g0014 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.173+587A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500449 | |||||||
| chr22:41500764 | T | C | 7 | a0001c0001t0001g0156 a0001c0001t0002g0151 a0001c0001t0002g0153 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.173+902T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41500764 | |||||||
| chr22:41501010 | A | AT | 8 | a0001c0001t0001g0282 a0001c0002t0001g0002 a0001c0002t0001g0029 others(5): Show |
11 | HG00408.hp2 HG00544.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.173+1159dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41501010 | ||||||
| chr22:41501239 | C | T | 1 | a0001c0002t0001g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.173+1377C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41501239 | |||||||
| chr22:41501515 | A | C | 2 | a0001c0001t0001g0156 a0001c0010t0001g0157 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.173+1653A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41501515 | |||||||
| chr22:41501707 | T | C | 1 | a0004c0011t0001g0260 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.173+1845T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41501707 | |||||||
| chr22:41501759 | C | G | 4 | a0001c0003t0001g0036 a0001c0003t0001g0043 a0001c0003t0001g0088 others(1): Show |
4 | NA18962.hp1 NA18963.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.173+1897C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41501759 | |||||||
| chr22:41501798 | C | G | 1 | a0001c0002t0001g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.173+1936C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41501798 | |||||||
| chr22:41502378 | G | A | 4 | a0001c0002t0001g0014 a0001c0002t0001g0253 a0001c0002t0001g0254 others(1): Show |
5 | HG02559.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.173+2516G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41502378 | |||||||
| chr22:41502501 | G | A | 2 | a0001c0003t0001g0052 a0001c0003t0001g0060 |
2 | HG00621.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.173+2639G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41502501 | |||||||
| chr22:41502909 | C | CT | 12 | a0001c0001t0001g0261 a0001c0001t0001g0278 a0001c0001t0001g0284 others(9): Show |
12 | HG00673.hp1 HG02080.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.173+3058dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41502909 | ||||||
| chr22:41503065 | A | G | 1 | a0001c0003t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.173+3203A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503065 | |||||||
| chr22:41503246 | C | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0178 a0001c0001t0001g0184 others(1): Show |
5 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.173+3384C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503246 | |||||||
| chr22:41503336 | T | C | 1 | a0001c0002t0001g0254 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.173+3474T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503336 | |||||||
| chr22:41503365 | C | T | 2 | a0001c0002t0001g0104 a0001c0002t0001g0117 |
2 | HG01069.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.173+3503C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503365 | |||||||
| chr22:41503366 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0273 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.173+3504G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503366 | |||||||
| chr22:41503377 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.173+3515C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503377 | |||||||
| chr22:41503455 | C | T | 1 | a0001c0002t0001g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.173+3593C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503455 | |||||||
| chr22:41503539 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0235 |
2 | HG02040.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.173+3677C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503539 | |||||||
| chr22:41503594 | G | A | 4 | a0001c0002t0001g0104 a0001c0002t0001g0109 a0001c0002t0001g0113 others(1): Show |
4 | HG01069.hp2 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.173+3732G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503594 | |||||||
| chr22:41503620 | C | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0288 |
2 | NA18959.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.173+3758C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503620 | |||||||
| chr22:41503872 | G | T | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.174-3919G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503872 | |||||||
| chr22:41503918 | A | G | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.174-3873A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503918 | |||||||
| chr22:41503935 | C | T | 3 | a0001c0002t0001g0166 a0001c0002t0001g0167 a0002c0008t0001g0159 |
3 | HG02886.hp1 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.174-3856C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503935 | |||||||
| chr22:41503964 | G | A | 1 | a0001c0002t0001g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.174-3827G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503964 | |||||||
| chr22:41503988 | C | T | 1 | a0001c0005t0001g0164 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.174-3803C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503988 | |||||||
| chr22:41503989 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.174-3802G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41503989 | |||||||
| chr22:41504076 | C | A | 1 | a0001c0003t0001g0027 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.174-3715C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504076 | |||||||
| chr22:41504086 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.174-3705A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504086 | |||||||
| chr22:41504089 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(72): Show |
79 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.174-3702G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504089 | |||||||
| chr22:41504293 | G | A | 14 | a0001c0002t0001g0014 a0001c0002t0001g0160 a0001c0002t0001g0161 others(11): Show |
15 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.174-3498G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504293 | |||||||
| chr22:41504336 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174-3455C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504336 | |||||||
| chr22:41504435 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(79): Show |
86 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.174-3356A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504435 | |||||||
| chr22:41504614 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0276 |
2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.174-3177C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504614 | |||||||
| chr22:41504709 | G | A | 1 | a0001c0005t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.174-3082G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504709 | |||||||
| chr22:41504709 | G | GA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
136 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.174-3081dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41504709 | ||||||
| chr22:41504710 | A | AAC | 26 | a0001c0001t0001g0084 a0001c0001t0001g0165 a0001c0001t0001g0172 others(23): Show |
27 | HG00639.hp1 HG01099.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.174-3081_174-3080i others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504710 | |||||||
| chr22:41504710 | A | AACT | 3 | a0001c0001t0001g0176 a0001c0001t0001g0196 a0001c0005t0001g0164 |
3 | HG01261.hp1 HG01981.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.174-3081_174-3080i others(5): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504710 | |||||||
| chr22:41504711 | C | A | 14 | a0001c0001t0001g0190 a0001c0001t0001g0194 a0001c0001t0001g0201 others(11): Show |
14 | HG00280.hp2 HG01070.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.174-3080C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504711 | |||||||
| chr22:41504711 | C | CT | 34 | a0001c0002t0001g0066 a0001c0002t0001g0092 a0001c0002t0001g0094 others(31): Show |
35 | HG00408.hp2 HG00741.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.174-3050dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41504711 | ||||||
| chr22:41504711 | C | T | 29 | a0001c0001t0001g0084 a0001c0001t0001g0165 a0001c0001t0001g0172 others(26): Show |
30 | HG00639.hp1 HG01099.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.174-3080C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504711 | |||||||
| chr22:41504711 | CT | C | 8 | a0001c0002t0001g0110 a0001c0002t0001g0123 a0001c0002t0001g0131 others(5): Show |
8 | HG00140.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.174-3050delT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41504711 | ||||||
| chr22:41504711 | CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0001g0080 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.174-3062_174-3050d others(15): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41504711 | ||||||
| chr22:41504712 | T | A | 2 | a0001c0004t0001g0139 a0001c0004t0001g0140 |
2 | HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.174-3079T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504712 | |||||||
| chr22:41504712 | T | C | 14 | a0001c0001t0001g0190 a0001c0001t0001g0194 a0001c0001t0001g0201 others(11): Show |
14 | HG00280.hp2 HG01070.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.174-3079T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504712 | |||||||
| chr22:41504712 | T | G | 1 | a0001c0001t0001g0252 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.174-3079T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504712 | |||||||
| chr22:41504713 | T | C | 2 | a0001c0004t0001g0139 a0001c0004t0001g0140 |
2 | HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.174-3078T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504713 | |||||||
| chr22:41504829 | T | G | 1 | a0002c0008t0001g0159 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.174-2962T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504829 | |||||||
| chr22:41504842 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.174-2949G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41504842 | |||||||
| chr22:41505289 | G | A | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.174-2502G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41505289 | |||||||
| chr22:41505424 | TAAC | T | 3 | a0001c0003t0001g0021 a0001c0003t0001g0050 a0001c0003t0001g0063 |
3 | HG02083.hp1 HG02132.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.174-2364_174-2362d others(5): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41505424 | ||||||
| chr22:41505427 | C | CAAT | 52 | a0001c0001t0001g0146 a0001c0001t0001g0169 a0001c0001t0001g0172 others(49): Show |
55 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.174-2339_174-2337d others(5): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41505427 | ||||||
| chr22:41505427 | C | CAATAATA others(5): Show |
1 | a0001c0004t0001g0140 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.174-2348_174-2337d others(14): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 41505427 | ||||||
| chr22:41505540 | G | A | 1 | a0001c0003t0001g0053 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.174-2251G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41505540 | |||||||
| chr22:41505642 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.174-2149C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41505642 | |||||||
| chr22:41505747 | A | G | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG01109.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.174-2044A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41505747 | |||||||
| chr22:41505833 | T | G | 1 | a0001c0003t0001g0036 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.174-1958T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41505833 | |||||||
| chr22:41506077 | G | T | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.174-1714G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506077 | |||||||
| chr22:41506080 | T | G | 1 | a0001c0004t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.174-1711T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506080 | |||||||
| chr22:41506084 | T | G | 1 | a0001c0004t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.174-1707T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506084 | |||||||
| chr22:41506242 | C | G | 1 | a0001c0003t0001g0141 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.174-1549C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506242 | |||||||
| chr22:41506314 | G | A | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.174-1477G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506314 | |||||||
| chr22:41506455 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.174-1336A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506455 | |||||||
| chr22:41506499 | T | C | 57 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(54): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.174-1292T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506499 | |||||||
| chr22:41506516 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.174-1275G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506516 | |||||||
| chr22:41506965 | C | T | 3 | a0001c0003t0001g0021 a0001c0003t0001g0050 a0001c0003t0001g0063 |
3 | HG02083.hp1 HG02132.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.174-826C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506965 | |||||||
| chr22:41506971 | G | A | 5 | a0001c0002t0001g0014 a0001c0002t0001g0253 a0001c0002t0001g0254 others(2): Show |
6 | HG02559.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.174-820G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41506971 | |||||||
| chr22:41507025 | C | G | 1 | a0001c0002t0001g0116 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.174-766C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41507025 | |||||||
| chr22:41507036 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(78): Show |
85 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.174-755C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41507036 | |||||||
| chr22:41507216 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.174-575G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41507216 | |||||||
| chr22:41507468 | C | T | 10 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0269 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.174-323C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41507468 | |||||||
| chr22:41507591 | C | T | 1 | a0001c0003t0001g0141 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.174-200C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41507591 | |||||||
| chr22:41507737 | G | A | 1 | a0001c0003t0001g0056 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.174-54G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41507737 | |||||||
| chr22:41507739 | G | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(169): Show |
182 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.174-52G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 2/17 | chr22 | 41507739 | |||||||
| chr22:41508109 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG01109.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+60C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41508109 | |||||||
| chr22:41508243 | G | A | 1 | a0001c0003t0001g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.432+194G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41508243 | |||||||
| chr22:41508429 | C | T | 2 | a0001c0002t0001g0103 a0001c0002t0001g0115 |
2 | NA18979.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.432+380C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41508429 | |||||||
| chr22:41508503 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.432+454G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41508503 | |||||||
| chr22:41508762 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.432+713A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41508762 | |||||||
| chr22:41508834 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.432+785G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41508834 | |||||||
| chr22:41509007 | T | C | 1 | a0001c0005t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.432+958T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509007 | |||||||
| chr22:41509143 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.432+1094A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509143 | |||||||
| chr22:41509274 | T | C | 56 | a0001c0001t0001g0068 a0001c0002t0001g0042 a0001c0002t0001g0065 others(53): Show |
59 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.432+1225T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509274 | |||||||
| chr22:41509666 | G | GA | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+1618dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr22 | 41509666 | ||||||
| chr22:41509744 | G | A | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+1695G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509744 | |||||||
| chr22:41509759 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.432+1710G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509759 | |||||||
| chr22:41509810 | A | G | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.432+1761A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509810 | |||||||
| chr22:41509813 | G | GTA | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+1765_432+1766i others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr22 | 41509813 | ||||||
| chr22:41509815 | C | CT | 201 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(198): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.432+1786dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr22 | 41509815 | ||||||
| chr22:41509815 | C | CTT | 54 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
58 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.432+1785_432+1786d others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr22 | 41509815 | ||||||
| chr22:41509815 | C | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+1766C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509815 | |||||||
| chr22:41509834 | T | G | 1 | a0001c0002t0001g0120 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.432+1785T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509834 | |||||||
| chr22:41509835 | T | A | 1 | a0001c0002t0001g0120 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.432+1786T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41509835 | |||||||
| chr22:41509881 | ACAATCTC others(9): Show |
A | 1 | a0001c0003t0001g0022 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.432+1852_432+1867d others(18): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr22 | 41509881 | ||||||
| chr22:41510088 | G | A | 1 | a0001c0005t0001g0164 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.433-1788G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41510088 | |||||||
| chr22:41510221 | CAGAGATG others(22): Show |
C | 1 | a0001c0001t0001g0175 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.433-1651_433-1623d others(31): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr22 | 41510221 | ||||||
| chr22:41510253 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.433-1623A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41510253 | |||||||
| chr22:41510321 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
52 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.433-1555C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41510321 | |||||||
| chr22:41510599 | G | A | 1 | a0001c0002t0001g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.433-1277G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41510599 | |||||||
| chr22:41510823 | C | A | 2 | a0001c0003t0001g0049 a0001c0003t0001g0061 |
2 | HG01081.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.433-1053C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41510823 | |||||||
| chr22:41510852 | G | C | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1024G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41510852 | |||||||
| chr22:41510878 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG01109.hp1 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-998C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41510878 | |||||||
| chr22:41511008 | G | T | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.433-868G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511008 | |||||||
| chr22:41511068 | C | T | 2 | a0001c0002t0001g0109 a0001c0002t0001g0113 |
2 | HG01346.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.433-808C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511068 | |||||||
| chr22:41511123 | G | T | 1 | a0001c0003t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.433-753G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511123 | |||||||
| chr22:41511144 | G | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.433-732G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511144 | |||||||
| chr22:41511167 | TTATTTTA others(12): Show |
T | 1 | a0001c0001t0001g0174 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433-707_433-689del others(19): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr22 | 41511167 | ||||||
| chr22:41511248 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.433-628T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511248 | |||||||
| chr22:41511281 | T | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(306): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.433-595T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511281 | |||||||
| chr22:41511394 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0030 a0001c0002t0001g0031 others(1): Show |
5 | HG02965.hp1 HG03130.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-482A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511394 | |||||||
| chr22:41511467 | C | T | 4 | a0001c0004t0001g0138 a0001c0004t0001g0139 a0001c0004t0001g0140 others(1): Show |
4 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-409C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511467 | |||||||
| chr22:41511774 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.433-102T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 3/17 | chr22 | 41511774 | |||||||
| chr22:41512105 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.525+137C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41512105 | |||||||
| chr22:41512107 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.525+139C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41512107 | |||||||
| chr22:41512401 | T | C | 54 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
58 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.525+433T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41512401 | |||||||
| chr22:41512512 | G | A | 1 | a0001c0003t0001g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.525+544G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41512512 | |||||||
| chr22:41512783 | G | A | 1 | a0001c0004t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.525+815G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41512783 | |||||||
| chr22:41512859 | A | T | 1 | a0001c0003t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.525+891A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41512859 | |||||||
| chr22:41512877 | T | C | 2 | a0001c0002t0001g0253 a0001c0002t0001g0254 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.525+909T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41512877 | |||||||
| chr22:41513010 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0197 |
2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.525+1042C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513010 | |||||||
| chr22:41513025 | C | A | 1 | a0001c0003t0001g0072 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.525+1057C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513025 | |||||||
| chr22:41513060 | C | G | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.525+1092C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513060 | |||||||
| chr22:41513181 | T | C | 16 | a0001c0001t0001g0156 a0001c0001t0002g0151 a0001c0002t0001g0014 others(13): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.525+1213T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513181 | |||||||
| chr22:41513205 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0268 a0001c0001t0001g0273 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+1237G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513205 | |||||||
| chr22:41513238 | A | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0198 |
2 | HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.525+1270A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513238 | |||||||
| chr22:41513240 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.525+1272G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513240 | |||||||
| chr22:41513340 | G | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(77): Show |
84 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.525+1372G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513340 | |||||||
| chr22:41513498 | G | A | 1 | a0001c0003t0001g0143 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.525+1530G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513498 | |||||||
| chr22:41513541 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.525+1573G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513541 | |||||||
| chr22:41513614 | T | TC | 264 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(261): Show |
279 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.525+1648dupC | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr22 | 41513614 | ||||||
| chr22:41513873 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.526-1504C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513873 | |||||||
| chr22:41513907 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.526-1470C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41513907 | |||||||
| chr22:41513920 | A | ATGTGGAC others(17): Show |
1 | a0001c0003t0001g0041 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.526-1429_526-1406d others(26): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr22 | 41513920 | ||||||
| chr22:41513920 | ATGTGGAC others(17): Show |
A | 2 | a0001c0001t0001g0208 a0001c0002t0001g0081 |
2 | HG02630.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.526-1429_526-1406d others(26): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr22 | 41513920 | ||||||
| chr22:41514199 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0287 |
2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.526-1178T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41514199 | |||||||
| chr22:41514240 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
52 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.526-1137C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41514240 | |||||||
| chr22:41514555 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.526-822G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41514555 | |||||||
| chr22:41515081 | T | C | 2 | a0001c0003t0001g0022 a0001c0003t0001g0023 |
2 | NA18977.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.526-296T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41515081 | |||||||
| chr22:41515323 | T | G | 1 | a0001c0003t0001g0039 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.526-54T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 4/17 | chr22 | 41515323 | |||||||
| chr22:41515617 | A | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+82A>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 5/17 | chr22 | 41515617 | |||||||
| chr22:41515655 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.685-112G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 5/17 | chr22 | 41515655 | |||||||
| chr22:41515681 | T | C | 1 | a0001c0002t0001g0115 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.685-86T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 5/17 | chr22 | 41515681 | |||||||
| chr22:41516212 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.835+295A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41516212 | |||||||
| chr22:41516714 | C | A | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.835+797C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41516714 | |||||||
| chr22:41516746 | A | G | 55 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(52): Show |
59 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.836-781A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41516746 | |||||||
| chr22:41516808 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.836-719C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41516808 | |||||||
| chr22:41516857 | G | A | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.836-670G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41516857 | |||||||
| chr22:41516900 | A | AT | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.836-618dupT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 41516900 | ||||||
| chr22:41516929 | CA | C | 3 | a0001c0002t0001g0166 a0001c0002t0001g0167 a0002c0008t0001g0159 |
3 | HG02886.hp1 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.836-597delA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41516929 | |||||||
| chr22:41517397 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.836-130C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41517397 | |||||||
| chr22:41517409 | C | T | 81 | a0001c0003t0001g0003 a0001c0003t0001g0008 a0001c0003t0001g0015 others(78): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.836-118C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41517409 | |||||||
| chr22:41517469 | G | C | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.836-58G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41517469 | |||||||
| chr22:41517473 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(175): Show |
189 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.836-54T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 6/17 | chr22 | 41517473 | |||||||
| chr22:41517840 | A | G | 56 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.940+209A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 7/17 | chr22 | 41517840 | |||||||
| chr22:41517934 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.940+303C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 7/17 | chr22 | 41517934 | |||||||
| chr22:41518111 | G | C | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.941-370G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 7/17 | chr22 | 41518111 | |||||||
| chr22:41518123 | G | A | 2 | a0001c0003t0001g0026 a0001c0003t0001g0027 |
2 | NA18940.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.941-358G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 7/17 | chr22 | 41518123 | |||||||
| chr22:41518250 | C | T | 1 | a0001c0002t0001g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.941-231C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 7/17 | chr22 | 41518250 | |||||||
| chr22:41518430 | A | C | 7 | a0001c0003t0001g0015 a0001c0003t0001g0294 a0001c0003t0001g0295 others(4): Show |
8 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.941-51A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 7/17 | chr22 | 41518430 | |||||||
| chr22:41518449 | C | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0251 |
2 | HG04184.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.941-32C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 7/17 | chr22 | 41518449 | |||||||
| chr22:41518589 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(163): Show |
176 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1032+17C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41518589 | |||||||
| chr22:41518771 | T | TA | 14 | a0001c0001t0001g0156 a0001c0001t0001g0199 a0001c0002t0001g0160 others(11): Show |
14 | HG00408.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1032+216dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 41518771 | ||||||
| chr22:41518771 | TA | T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0114 a0001c0002t0001g0145 others(2): Show |
6 | HG01169.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032+216delA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 41518771 | ||||||
| chr22:41518856 | T | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(176): Show |
190 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1032+284T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41518856 | |||||||
| chr22:41519046 | G | T | 1 | a0001c0003t0001g0118 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1032+474G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41519046 | |||||||
| chr22:41519271 | G | C | 1 | a0001c0003t0001g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1032+699G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41519271 | |||||||
| chr22:41519325 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
52 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1032+753C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41519325 | |||||||
| chr22:41519373 | A | G | 1 | a0001c0002t0001g0120 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1033-798A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41519373 | |||||||
| chr22:41519436 | G | T | 1 | a0001c0003t0001g0039 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1033-735G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41519436 | |||||||
| chr22:41519505 | T | C | 1 | a0001c0004t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1033-666T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41519505 | |||||||
| chr22:41519699 | T | G | 1 | a0001c0002t0001g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1033-472T>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41519699 | |||||||
| chr22:41519807 | C | CAA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(115): Show |
124 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1033-351_1033-350d others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 41519807 | ||||||
| chr22:41519807 | C | CAAA | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1033-352_1033-350d others(5): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 41519807 | ||||||
| chr22:41519807 | C | CAG | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1033-363_1033-362i others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 41519807 | ||||||
| chr22:41519997 | C | G | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
52 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1033-174C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 8/17 | chr22 | 41519997 | |||||||
| chr22:41520534 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0265 a0001c0001t0001g0284 |
3 | HG00673.hp1 NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1138+258C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41520534 | |||||||
| chr22:41520609 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1138+333G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41520609 | |||||||
| chr22:41520638 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1138+362C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41520638 | |||||||
| chr22:41520726 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1138+450C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41520726 | |||||||
| chr22:41520757 | G | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0030 a0001c0002t0001g0031 |
4 | HG02965.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138+481G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41520757 | |||||||
| chr22:41520843 | G | GA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(88): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1138+582dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 41520843 | ||||||
| chr22:41520859 | T | A | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1138+583T>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41520859 | |||||||
| chr22:41520957 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1138+681G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41520957 | |||||||
| chr22:41521035 | C | CA | 46 | a0001c0001t0001g0019 a0001c0001t0001g0082 a0001c0001t0001g0083 others(43): Show |
47 | HG00558.hp1 HG00639.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1138+783dupA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 41521035 | ||||||
| chr22:41521035 | C | CAA | 8 | a0001c0001t0001g0214 a0001c0001t0001g0266 a0001c0001t0001g0267 others(5): Show |
8 | HG00621.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1138+782_1138+783d others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 41521035 | ||||||
| chr22:41521035 | CAAAAAAA others(2): Show |
C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0170 a0001c0001t0001g0174 others(8): Show |
12 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1138+775_1138+783d others(11): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 41521035 | ||||||
| chr22:41521035 | CAAAAAAA others(3): Show |
C | 38 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
41 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1138+774_1138+783d others(12): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 41521035 | ||||||
| chr22:41521035 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0104 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1138+772_1138+783d others(14): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 41521035 | ||||||
| chr22:41521056 | A | G | 5 | a0001c0001t0001g0183 a0001c0003t0001g0044 a0001c0003t0001g0074 others(2): Show |
5 | HG00733.hp1 HG01192.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138+780A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41521056 | |||||||
| chr22:41521441 | C | T | 3 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 |
3 | HG01243.hp2 HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1138+1165C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41521441 | |||||||
| chr22:41521464 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1138+1188T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41521464 | |||||||
| chr22:41521614 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG03195.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1139-1216C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41521614 | |||||||
| chr22:41521689 | G | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0210 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1139-1141G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41521689 | |||||||
| chr22:41521916 | C | T | 5 | a0001c0003t0001g0290 a0001c0003t0001g0293 a0001c0003t0001g0297 others(2): Show |
5 | HG00738.hp2 HG01081.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139-914C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41521916 | |||||||
| chr22:41521973 | G | T | 2 | a0001c0006t0002g0152 a0001c0006t0002g0155 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1139-857G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41521973 | |||||||
| chr22:41521984 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1139-846G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41521984 | |||||||
| chr22:41522317 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1139-513C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41522317 | |||||||
| chr22:41522347 | C | G | 1 | a0001c0010t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1139-483C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41522347 | |||||||
| chr22:41522549 | C | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139-281C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41522549 | |||||||
| chr22:41522608 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(45): Show |
52 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1139-222A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41522608 | |||||||
| chr22:41522645 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1139-185A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | chr22 | 41522645 | |||||||
| chr22:41522649 | GT | G | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1139-179delT | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 41522649 | ||||||
| chr22:41523326 | A | G | 54 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
58 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1370+48A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 11/17 | chr22 | 41523326 | |||||||
| chr22:41523381 | A | G | 1 | a0002c0008t0001g0159 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1370+103A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 11/17 | chr22 | 41523381 | |||||||
| chr22:41523418 | C | A | 1 | a0002c0008t0001g0159 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1370+140C>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 11/17 | chr22 | 41523418 | |||||||
| chr22:41523425 | C | T | 2 | a0001c0002t0001g0166 a0001c0002t0001g0167 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1370+147C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 11/17 | chr22 | 41523425 | |||||||
| chr22:41523673 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1371-157C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 11/17 | chr22 | 41523673 | |||||||
| chr22:41523688 | A | C | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1371-142A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 11/17 | chr22 | 41523688 | |||||||
| chr22:41523783 | G | T | 3 | a0001c0003t0001g0133 a0001c0003t0001g0134 a0001c0003t0001g0136 |
3 | HG01884.hp2 HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1371-47G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 11/17 | chr22 | 41523783 | |||||||
| chr22:41523957 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1482+16T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 12/17 | chr22 | 41523957 | |||||||
| chr22:41524079 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1482+138G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 12/17 | chr22 | 41524079 | |||||||
| chr22:41524132 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1482+191T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 12/17 | chr22 | 41524132 | |||||||
| chr22:41524460 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1483-386T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 12/17 | chr22 | 41524460 | |||||||
| chr22:41524685 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1483-161A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 12/17 | chr22 | 41524685 | |||||||
| chr22:41524707 | C | G | 1 | a0001c0005t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1483-139C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 12/17 | chr22 | 41524707 | |||||||
| chr22:41524809 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1483-37T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 12/17 | chr22 | 41524809 | |||||||
| chr22:41524991 | T | C | 1 | a0001c0002t0001g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1605+23T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 13/17 | chr22 | 41524991 | |||||||
| chr22:41525061 | G | A | 5 | a0001c0002t0001g0160 a0001c0002t0001g0161 a0001c0002t0001g0162 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1605+93G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 13/17 | chr22 | 41525061 | |||||||
| chr22:41525087 | G | A | 6 | a0001c0002t0001g0007 a0001c0002t0001g0033 a0001c0002t0001g0034 others(3): Show |
7 | HG02280.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1606-106G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 13/17 | chr22 | 41525087 | |||||||
| chr22:41525170 | C | T | 2 | a0001c0006t0002g0152 a0001c0006t0002g0155 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1606-23C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 13/17 | chr22 | 41525170 | |||||||
| chr22:41525173 | A | G | 2 | a0001c0002t0001g0042 a0001c0002t0001g0086 |
2 | NA18955.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1606-20A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 13/17 | chr22 | 41525173 | |||||||
| chr22:41525554 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1761+206A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 14/17 | chr22 | 41525554 | |||||||
| chr22:41525661 | A | G | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1761+313A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 14/17 | chr22 | 41525661 | |||||||
| chr22:41525834 | GA | G | 14 | a0001c0001t0001g0309 a0001c0002t0001g0006 a0001c0002t0001g0030 others(11): Show |
15 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1762-427delA | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 14/17 | chr22 | 41525834 | |||||||
| chr22:41526104 | C | T | 1 | a0001c0003t0001g0028 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1762-158C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 14/17 | chr22 | 41526104 | |||||||
| chr22:41526182 | GCTGC | G | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1762-73_1762-70del others(4): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr22 | 41526182 | ||||||
| chr22:41526212 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1762-50C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 14/17 | chr22 | 41526212 | |||||||
| chr22:41526587 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1953+134G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41526587 | |||||||
| chr22:41526626 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1953+173C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41526626 | |||||||
| chr22:41526632 | G | GC | 5 | a0001c0002t0001g0007 a0001c0002t0001g0033 a0001c0002t0001g0034 others(2): Show |
6 | HG02280.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1953+182dupC | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr22 | 41526632 | ||||||
| chr22:41526639 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0069 a0001c0003t0001g0085 others(1): Show |
4 | HG00642.hp1 HG03831.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1953+186T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41526639 | |||||||
| chr22:41526809 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1953+356G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41526809 | |||||||
| chr22:41527071 | A | C | 2 | a0001c0002t0001g0034 a0002c0008t0001g0159 |
2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1954-217A>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41527071 | |||||||
| chr22:41527092 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1954-196C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41527092 | |||||||
| chr22:41527093 | G | A | 1 | a0001c0003t0001g0133 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1954-195G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41527093 | |||||||
| chr22:41527117 | C | T | 3 | a0001c0003t0001g0015 a0001c0003t0001g0295 a0001c0003t0001g0296 |
4 | HG00140.hp1 HG01070.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1954-171C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41527117 | |||||||
| chr22:41527176 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1954-112G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41527176 | |||||||
| chr22:41527217 | G | GCAGGTAG others(7): Show |
1 | a0001c0001t0001g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1954-65_1954-52dup others(14): Show |
ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr22 | 41527217 | ||||||
| chr22:41527256 | G | C | 3 | a0001c0002t0001g0162 a0001c0002t0001g0163 a0001c0003t0001g0135 |
3 | HG02809.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1954-32G>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41527256 | |||||||
| chr22:41527275 | G | A | 4 | a0001c0002t0001g0014 a0001c0002t0001g0253 a0001c0002t0001g0254 others(1): Show |
5 | HG02559.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1954-13G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41527275 | |||||||
| chr22:41527276 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1954-12C>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 15/17 | chr22 | 41527276 | |||||||
| chr22:41527640 | G | A | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
56 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.2086+220G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 16/17 | chr22 | 41527640 | |||||||
| chr22:41527647 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(120): Show |
130 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.2086+227T>C | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 16/17 | chr22 | 41527647 | |||||||
| chr22:41527825 | G | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2087-76G>T | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 16/17 | chr22 | 41527825 | |||||||
| chr22:41528097 | G | A | 1 | a0001c0003t0001g0058 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2208+75G>A | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 17/17 | chr22 | 41528097 | |||||||
| chr22:41528228 | A | G | 6 | a0001c0002t0001g0007 a0001c0002t0001g0033 a0001c0002t0001g0034 others(3): Show |
7 | HG02280.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2208+206A>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 17/17 | chr22 | 41528228 | |||||||
| chr22:41528401 | C | G | 5 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2209-78C>G | ACO2 | ENSG00000100412.17 | transcript | ENST00000216254.9 | protein_coding | 17/17 | chr22 | 41528401 |