Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 306 |
| ensemblid | ENSG00000138772.13 |
| hgncid | 541 |
| symbol | ANXA3 |
| name | annexin A3 |
| refseq_nuc | NM_005139.3 |
| refseq_prot | NP_005130.1 |
| ensembl_nuc | ENST00000264908.11 |
| ensembl_prot | ENSP00000264908.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 78551770 |
| end | 78610447 |
| strand | + |
| ver | v1.2 |
| region | chr4:78551770-78610447 |
| region5000 | chr4:78546770-78615447 |
| regionname0 | ANXA3_chr4_78551770_78610447 |
| regionname5000 | ANXA3_chr4_78546770_78615447 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 323 | 313 | 83 | 48 | 144 | 6 | 30 | 108 | ANXA3_chr4_78546770_78615447 | ANXA3 | MASIW others(318): Show |
chr4 | 78546770 | 78615447 |
| a0002 | 0/0 | 323 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | MASIW others(318): Show |
chr4 | 78546770 | 78615447 |
| a0003 | 0/0 | 323 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | MASIW others(318): Show |
chr4 | 78546770 | 78615447 |
| a0004 | 0/0 | 323 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | MASIW others(318): Show |
chr4 | 78546770 | 78615447 |
| a0005 | 0/0 | 323 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | MASIW others(318): Show |
chr4 | 78546770 | 78615447 |
| a0006 | 0/0 | 323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | MASIW others(318): Show |
chr4 | 78546770 | 78615447 |
| a0007 | 0/0 | 323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | MASIW others(318): Show |
chr4 | 78546770 | 78615447 |
| a0008 | 0/0 | 323 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | MASIW others(318): Show |
chr4 | 78546770 | 78615447 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 969 | 287 | 58 | 48 | 143 | 6 | 30 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0001c0002 | 0/0 | 969 | 23 | 23 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0001c0006 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0001c0011 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0001c0012 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0002c0003 | 0/0 | 969 | 6 | 6 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0003c0004 | 0/0 | 969 | 4 | 4 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0004c0007 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0004c0010 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0005c0005 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0006c0013 | 0/0 | 969 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0007c0008 | 0/0 | 969 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 | ||
| a0008c0009 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | ATGGC others(964): Show |
chr4 | 78546770 | 78615447 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1432 | 124 | 13 | 16 | 78 | 3 | 13 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0001t0002 | 1/0 | 1432 | 76 | 22 | 26 | 15 | 2 | 10 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0001t0003 | 0/0 | 1432 | 66 | 2 | 6 | 50 | 1 | 7 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0001t0004 | 0/0 | 1432 | 10 | 10 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0001t0005 | 0/0 | 1432 | 9 | 9 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0001t0006 | 0/0 | 1429 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1424): Show |
chr4 | 78546770 | 78615447 |
| a0001c0001t0007 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0002t0001 | 0/0 | 1432 | 16 | 16 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0002t0003 | 0/0 | 1432 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0002t0004 | 0/0 | 1432 | 3 | 3 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0002t0006 | 0/0 | 1429 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1424): Show |
chr4 | 78546770 | 78615447 |
| a0001c0006t0001 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0011t0008 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0001c0012t0001 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0002c0003t0004 | 0/0 | 1432 | 3 | 3 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0002c0003t0006 | 0/0 | 1429 | 3 | 3 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1424): Show |
chr4 | 78546770 | 78615447 |
| a0003c0004t0002 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0003c0004t0004 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0003c0004t0006 | 0/0 | 1429 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1424): Show |
chr4 | 78546770 | 78615447 |
| a0004c0007t0001 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0004c0010t0004 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0005c0005t0003 | 0/0 | 1432 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0006c0013t0003 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0007c0008t0002 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| a0008c0009t0001 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | AGCGC others(1427): Show |
chr4 | 78546770 | 78615447 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0002 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0004 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0005g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0002t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0011t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0001c0012t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0002c0003t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0002c0003t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0002c0003t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0002c0003t0006g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0002c0003t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0003c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0003c0004t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0003c0004t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0003c0004t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0004c0007t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0004c0010t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0005c0005t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0005c0005t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0006c0013t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0007c0008t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| a0008c0009t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0192 | EUR | FIN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0137 | EUR | FIN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00423 | hp1 | a0001 | c0006 | t0001 | g0237 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01884 | hp1 | a0003 | c0004 | t0004 | g0286 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01891 | hp1 | a0001 | c0002 | t0006 | g0147 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01891 | hp2 | a0004 | c0010 | t0004 | g0155 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02145 | hp2 | a0002 | c0003 | t0004 | g0061 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02155 | hp2 | a0004 | c0007 | t0001 | g0274 | EAS | CDX | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02258 | hp1 | a0002 | c0003 | t0006 | g0135 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02280 | hp2 | a0003 | c0004 | t0006 | g0081 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | KHV | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02572 | hp2 | a0002 | c0003 | t0004 | g0060 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0148 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02809 | hp1 | a0002 | c0003 | t0004 | g0149 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02818 | hp1 | a0003 | c0004 | t0002 | g0082 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0283 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0277 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0068 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0050 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0058 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0052 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03486 | hp2 | a0005 | c0005 | t0003 | g0080 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03516 | hp1 | a0001 | c0011 | t0008 | g0084 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0054 | AFR | ESN | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03831 | hp2 | a0006 | c0013 | t0003 | g0222 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0288 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG04204 | hp2 | a0007 | c0008 | t0002 | g0134 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18522 | hp1 | a0003 | c0004 | t0006 | g0083 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18612 | hp1 | a0008 | c0009 | t0001 | g0182 | EAS | CHB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | CHB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18906 | hp2 | a0002 | c0003 | t0006 | g0011 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19030 | hp1 | a0001 | c0012 | t0001 | g0279 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19043 | hp2 | a0005 | c0005 | t0003 | g0063 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA20129 | hp1 | a0002 | c0003 | t0006 | g0011 | AFR | ASW | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ASW | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0062 | AFR | ACB | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | USA | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | USA | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | USA | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | LWK | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0188 | REF | REF | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | ANXA3_chr4_78546770_78615447 | ANXA3 | chr4 | 78546770 | 78615447 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:78573220 | G | A | 1 | a0003 | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.56G>A | p.Ser19Asn | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/13 | 184/1432 | 56/972 | 19/323 | chr4 | 78573220 | |||
| chr4:78579027 | G | T | 1 | a0006 | 1 | HG03831.hp2 | missense_variant&splice_region_variant | MODERATE | c.104G>T | p.Gly35Val | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/13 | 232/1432 | 104/972 | 35/323 | chr4 | 78579027 | |||
| chr4:78586263 | G | A | 1 | a0004 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.316G>A | p.Ala106Thr | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/13 | 444/1432 | 316/972 | 106/323 | chr4 | 78586263 | |||
| chr4:78586264 | C | T | 1 | a0004 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.317C>T | p.Ala106Val | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/13 | 445/1432 | 317/972 | 106/323 | chr4 | 78586264 | |||
| chr4:78586326 | G | A | 1 | a0007 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.379G>A | p.Asp127Asn | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/13 | 507/1432 | 379/972 | 127/323 | chr4 | 78586326 | |||
| chr4:78597340 | T | A | 1 | a0002 | 6 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.656T>A | p.Ile219Asn | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/13 | 784/1432 | 656/972 | 219/323 | chr4 | 78597340 | |||
| chr4:78601528 | C | T | 1 | a0008 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.749C>T | p.Thr250Met | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/13 | 877/1432 | 749/972 | 250/323 | chr4 | 78601528 | |||
| chr4:78610081 | T | C | 1 | a0005 | 2 | HG03486.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.938T>C | p.Ile313Thr | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 1066/1432 | 938/972 | 313/323 | chr4 | 78610081 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:78579031 | T | A | 1 | a0006c0013 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.108T>A | p.Thr36Thr | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/13 | 236/1432 | 108/972 | 36/323 | chr4 | 78579031 | |||
| chr4:78579073 | T | C | 1 | a0001c0006 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.150T>C | p.Asn50Asn | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/13 | 278/1432 | 150/972 | 50/323 | chr4 | 78579073 | |||
| chr4:78582248 | A | G | 3 | a0001c0002 a0001c0011 a0001c0012 |
25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
synonymous_variant | LOW | c.270A>G | p.Pro90Pro | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/13 | 398/1432 | 270/972 | 90/323 | chr4 | 78582248 | |||
| chr4:78586265 | G | T | 3 | a0001c0002 a0001c0011 a0001c0012 |
25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
synonymous_variant | LOW | c.318G>T | p.Ala106Ala | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/13 | 446/1432 | 318/972 | 106/323 | chr4 | 78586265 | |||
| chr4:78591578 | C | T | 1 | a0001c0012 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.438C>T | p.Ser146Ser | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/13 | 566/1432 | 438/972 | 146/323 | chr4 | 78591578 | |||
| chr4:78597320 | A | G | 1 | a0001c0011 | 1 | HG03516.hp1 | splice_region_variant&synonymous_variant | LOW | c.636A>G | p.Thr212Thr | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/13 | 764/1432 | 636/972 | 212/323 | chr4 | 78597320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:78551791 | C | G | 1 | a0001c0011t0008 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/13 | 2683 | chr4 | 78551791 | ||||||
| chr4:78610154 | C | T | 7 | a0001c0001t0001 a0001c0002t0001 a0001c0006t0001 others(4): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 39 | chr4 | 78610154 | ||||||
| chr4:78610227 | T | G | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(3): Show |
81 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*112T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 112 | chr4 | 78610227 | ||||||
| chr4:78610250 | TAAC | T | 4 | a0001c0001t0006 a0001c0002t0006 a0002c0003t0006 others(1): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*147_*149delCAA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 147 | INFO_REALIGN_3_PRIME | chr4 | 78610250 | |||||
| chr4:78610367 | T | A | 1 | a0001c0001t0005 | 9 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*252T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 252 | chr4 | 78610367 | ||||||
| chr4:78610399 | C | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
251 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*284C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 284 | chr4 | 78610399 | ||||||
| chr4:78610434 | T | G | 1 | a0001c0001t0007 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*319T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 13/13 | 319 | chr4 | 78610434 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:78551902 | A | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(256): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-39+43A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78551902 | |||||||
| chr4:78551949 | G | T | 1 | a0001c0001t0003g0288 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-39+90G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78551949 | |||||||
| chr4:78551982 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-39+123G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78551982 | |||||||
| chr4:78552035 | C | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(226): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-39+176C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552035 | |||||||
| chr4:78552121 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(61): Show |
74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-39+262G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552121 | |||||||
| chr4:78552130 | G | A | 1 | a0001c0001t0005g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-39+271G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552130 | |||||||
| chr4:78552216 | C | T | 3 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 |
3 | HG00323.hp1 HG01106.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-39+357C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552216 | |||||||
| chr4:78552240 | A | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(61): Show |
74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-39+381A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552240 | |||||||
| chr4:78552314 | C | T | 1 | a0001c0001t0002g0287 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-39+455C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552314 | |||||||
| chr4:78552369 | T | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(65): Show |
78 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-39+510T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552369 | |||||||
| chr4:78552417 | G | A | 10 | a0001c0001t0001g0057 a0001c0001t0002g0065 a0001c0001t0002g0066 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+558G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552417 | |||||||
| chr4:78552458 | T | C | 10 | a0001c0001t0001g0057 a0001c0001t0002g0065 a0001c0001t0002g0066 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+599T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552458 | |||||||
| chr4:78552529 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-39+670T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552529 | |||||||
| chr4:78552548 | A | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(66): Show |
79 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-39+689A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552548 | |||||||
| chr4:78552580 | TA | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(65): Show |
78 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-39+722delA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552580 | |||||||
| chr4:78552643 | C | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(63): Show |
75 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-39+784C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552643 | |||||||
| chr4:78552886 | C | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0024 others(179): Show |
210 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-39+1027C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78552886 | |||||||
| chr4:78553075 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-39+1216T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553075 | |||||||
| chr4:78553161 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-38-1275C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553161 | |||||||
| chr4:78553237 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-38-1199C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553237 | |||||||
| chr4:78553306 | G | A | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-38-1130G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553306 | |||||||
| chr4:78553349 | A | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(134): Show |
161 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-38-1087A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553349 | |||||||
| chr4:78553428 | C | T | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(1): Show |
4 | HG02129.hp2 HG02155.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-1008C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553428 | |||||||
| chr4:78553471 | A | G | 8 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0002g0013 others(5): Show |
9 | HG00733.hp1 HG01070.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38-965A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553471 | |||||||
| chr4:78553552 | T | C | 6 | a0001c0001t0004g0151 a0001c0001t0007g0152 a0001c0002t0001g0150 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-884T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553552 | |||||||
| chr4:78553613 | T | C | 10 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(7): Show |
10 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-823T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553613 | |||||||
| chr4:78553658 | A | T | 6 | a0001c0001t0004g0151 a0001c0001t0007g0152 a0001c0002t0001g0150 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-778A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553658 | |||||||
| chr4:78553665 | A | G | 71 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0085 others(68): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-38-771A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553665 | |||||||
| chr4:78553681 | C | G | 5 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(2): Show |
5 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-755C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553681 | |||||||
| chr4:78553732 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
235 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.-38-704T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553732 | |||||||
| chr4:78553808 | C | A | 20 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0002g0066 others(17): Show |
21 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-38-628C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553808 | |||||||
| chr4:78553900 | C | A | 2 | a0001c0001t0004g0070 a0001c0001t0004g0071 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-38-536C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78553900 | |||||||
| chr4:78554192 | A | AT | 14 | a0001c0001t0004g0086 a0001c0002t0001g0032 a0001c0002t0001g0049 others(11): Show |
14 | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38-237dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 78554192 | ||||||
| chr4:78554288 | A | G | 3 | a0001c0001t0003g0017 a0001c0002t0006g0277 a0004c0010t0004g0155 |
4 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-148A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78554288 | |||||||
| chr4:78554403 | T | C | 1 | a0001c0002t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-38-33T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 1/12 | chr4 | 78554403 | |||||||
| chr4:78554606 | A | T | 3 | a0001c0001t0001g0205 a0001c0001t0002g0206 a0001c0001t0003g0127 |
3 | HG01106.hp1 HG02273.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.15+118A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78554606 | |||||||
| chr4:78554882 | A | G | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.15+394A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78554882 | |||||||
| chr4:78554907 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.15+419A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78554907 | |||||||
| chr4:78555032 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.15+544C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555032 | |||||||
| chr4:78555036 | T | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0207 a0001c0001t0001g0209 others(6): Show |
9 | HG00621.hp2 HG02056.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+548T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555036 | |||||||
| chr4:78555248 | T | G | 19 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0002g0066 others(16): Show |
20 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.15+760T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555248 | |||||||
| chr4:78555250 | T | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(218): Show |
254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.15+762T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555250 | |||||||
| chr4:78555267 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(218): Show |
254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.15+779A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555267 | |||||||
| chr4:78555350 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0003g0269 |
2 | NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.15+862C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555350 | |||||||
| chr4:78555394 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.15+906A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555394 | |||||||
| chr4:78555402 | T | A | 1 | a0001c0001t0003g0017 | 2 | HG00735.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.15+914T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555402 | |||||||
| chr4:78555405 | G | A | 2 | a0001c0001t0004g0070 a0001c0001t0004g0071 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.15+917G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555405 | |||||||
| chr4:78555674 | TA | T | 28 | a0001c0001t0001g0037 a0001c0001t0001g0267 a0001c0001t0002g0065 others(25): Show |
30 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.15+1204delA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78555674 | ||||||
| chr4:78555688 | A | AC | 3 | a0001c0001t0001g0207 a0001c0001t0003g0208 a0001c0011t0008g0084 |
3 | HG02056.hp2 HG02523.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+1200_15+1201ins others(1): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555688 | |||||||
| chr4:78555688 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(181): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.15+1200A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555688 | |||||||
| chr4:78555714 | T | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
255 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.15+1226T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555714 | |||||||
| chr4:78555721 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.15+1233T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555721 | |||||||
| chr4:78555722 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(190): Show |
224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.15+1234G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78555722 | |||||||
| chr4:78555852 | T | TA | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(169): Show |
203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.15+1376dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78555852 | ||||||
| chr4:78556141 | G | A | 4 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1653G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556141 | |||||||
| chr4:78556212 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.15+1724G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556212 | |||||||
| chr4:78556410 | C | G | 1 | a0001c0011t0008g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15+1922C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556410 | |||||||
| chr4:78556700 | C | T | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0002t0001g0087 |
3 | HG02572.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.15+2212C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556700 | |||||||
| chr4:78556781 | C | T | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.15+2293C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556781 | |||||||
| chr4:78556783 | C | G | 1 | a0001c0001t0002g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.15+2295C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78556783 | |||||||
| chr4:78557145 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.15+2657G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557145 | |||||||
| chr4:78557181 | C | T | 10 | a0001c0001t0001g0262 a0001c0001t0001g0266 a0001c0001t0001g0276 others(7): Show |
11 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+2693C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557181 | |||||||
| chr4:78557251 | A | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
255 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.15+2763A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557251 | |||||||
| chr4:78557482 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(283): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.15+2994A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557482 | |||||||
| chr4:78557523 | G | C | 1 | a0001c0001t0002g0022 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.15+3035G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557523 | |||||||
| chr4:78557582 | G | A | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG00597.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+3094G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557582 | |||||||
| chr4:78557636 | C | A | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.15+3148C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557636 | |||||||
| chr4:78557689 | CT | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(192): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.15+3220delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78557689 | ||||||
| chr4:78557693 | T | C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0261 a0001c0001t0002g0065 others(11): Show |
14 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+3205T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557693 | |||||||
| chr4:78557694 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(189): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.15+3206T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557694 | |||||||
| chr4:78557695 | T | C | 1 | a0001c0001t0003g0269 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.15+3207T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557695 | |||||||
| chr4:78557708 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+3220T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557708 | |||||||
| chr4:78557844 | A | G | 5 | a0001c0001t0003g0017 a0001c0001t0005g0058 a0001c0001t0005g0059 others(2): Show |
6 | HG00735.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+3356A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78557844 | |||||||
| chr4:78558019 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.15+3531C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558019 | |||||||
| chr4:78558219 | G | A | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.15+3731G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558219 | |||||||
| chr4:78558396 | C | T | 7 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0002g0013 others(4): Show |
8 | HG00733.hp1 HG01070.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+3908C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558396 | |||||||
| chr4:78558418 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.15+3930G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558418 | |||||||
| chr4:78558510 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.15+4022G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558510 | |||||||
| chr4:78558529 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.15+4041G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558529 | |||||||
| chr4:78558576 | C | T | 3 | a0001c0001t0003g0017 a0001c0002t0006g0277 a0004c0010t0004g0155 |
4 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4088C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558576 | |||||||
| chr4:78558579 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(180): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.15+4091T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558579 | |||||||
| chr4:78558728 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(190): Show |
224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.15+4240C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558728 | |||||||
| chr4:78558762 | A | C | 1 | a0001c0001t0003g0198 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.15+4274A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558762 | |||||||
| chr4:78558918 | G | A | 8 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0002t0001g0064 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+4430G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78558918 | |||||||
| chr4:78559117 | T | A | 1 | a0001c0001t0003g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.15+4629T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559117 | |||||||
| chr4:78559183 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0214 |
2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.15+4695G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559183 | |||||||
| chr4:78559255 | A | C | 24 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0002g0066 others(21): Show |
25 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.15+4767A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559255 | |||||||
| chr4:78559264 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.15+4776A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559264 | |||||||
| chr4:78559524 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0004g0055 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.15+5036G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559524 | |||||||
| chr4:78559761 | T | C | 8 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0002t0001g0064 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5273T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78559761 | |||||||
| chr4:78560030 | C | G | 3 | a0001c0001t0003g0017 a0001c0002t0006g0277 a0004c0010t0004g0155 |
4 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5542C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560030 | |||||||
| chr4:78560055 | C | G | 5 | a0001c0001t0001g0259 a0001c0001t0001g0268 a0001c0001t0002g0029 others(2): Show |
6 | HG01358.hp2 HG01934.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+5567C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560055 | |||||||
| chr4:78560374 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(193): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.15+5886T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560374 | |||||||
| chr4:78560424 | T | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(148): Show |
181 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.15+5936T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560424 | |||||||
| chr4:78560431 | G | A | 8 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(5): Show |
8 | HG02145.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5943G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560431 | |||||||
| chr4:78560603 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.15+6115G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560603 | |||||||
| chr4:78560644 | A | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(220): Show |
256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.15+6156A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560644 | |||||||
| chr4:78560840 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0258 |
3 | HG00280.hp2 HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.15+6352C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560840 | |||||||
| chr4:78560923 | T | A | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15+6435T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78560923 | |||||||
| chr4:78561012 | T | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(279): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.15+6524T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561012 | |||||||
| chr4:78561032 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(129): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.15+6544G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561032 | |||||||
| chr4:78561138 | C | T | 1 | a0001c0001t0003g0253 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.15+6650C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561138 | |||||||
| chr4:78561251 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+6763G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561251 | |||||||
| chr4:78561255 | A | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.15+6767A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561255 | |||||||
| chr4:78561555 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.15+7067T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561555 | |||||||
| chr4:78561578 | C | T | 4 | a0001c0001t0001g0266 a0001c0001t0001g0276 a0001c0001t0002g0287 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+7090C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561578 | |||||||
| chr4:78561639 | T | A | 3 | a0001c0001t0001g0102 a0001c0001t0002g0101 a0001c0001t0003g0103 |
3 | HG02155.hp1 NA18945.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.15+7151T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561639 | |||||||
| chr4:78561808 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0002g0260 |
2 | NA18951.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.15+7320A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561808 | |||||||
| chr4:78561828 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(283): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.15+7340A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561828 | |||||||
| chr4:78561950 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.15+7462A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561950 | |||||||
| chr4:78561965 | A | G | 1 | a0001c0001t0003g0197 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.15+7477A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78561965 | |||||||
| chr4:78562184 | G | A | 67 | a0001c0001t0001g0085 a0001c0001t0001g0133 a0001c0001t0001g0167 others(64): Show |
75 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.15+7696G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562184 | |||||||
| chr4:78562227 | G | GA | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(196): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.15+7746dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78562227 | ||||||
| chr4:78562281 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(107): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.15+7793A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562281 | |||||||
| chr4:78562398 | G | C | 1 | a0001c0001t0003g0216 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.15+7910G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562398 | |||||||
| chr4:78562438 | T | A | 1 | a0005c0005t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.15+7950T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562438 | |||||||
| chr4:78562498 | G | A | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+8010G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562498 | |||||||
| chr4:78562704 | T | C | 1 | a0001c0011t0008g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15+8216T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562704 | |||||||
| chr4:78562716 | T | C | 1 | a0001c0001t0002g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+8228T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562716 | |||||||
| chr4:78562717 | G | A | 22 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0002g0066 others(19): Show |
23 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+8229G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562717 | |||||||
| chr4:78562965 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.15+8477C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78562965 | |||||||
| chr4:78563148 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.15+8660C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563148 | |||||||
| chr4:78563162 | A | G | 1 | a0001c0011t0008g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15+8674A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563162 | |||||||
| chr4:78563238 | G | A | 67 | a0001c0001t0001g0085 a0001c0001t0001g0133 a0001c0001t0001g0167 others(64): Show |
75 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.15+8750G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563238 | |||||||
| chr4:78563297 | G | T | 2 | a0001c0001t0003g0017 a0004c0010t0004g0155 |
3 | HG00735.hp1 HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.15+8809G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563297 | |||||||
| chr4:78563333 | A | G | 2 | a0001c0001t0004g0151 a0001c0001t0007g0152 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.15+8845A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563333 | |||||||
| chr4:78563463 | G | GT | 2 | a0001c0001t0001g0028 a0001c0001t0001g0258 |
3 | HG00280.hp2 HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.15+8975_15+8976ins others(1): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563463 | |||||||
| chr4:78563506 | AG | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(118): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.15+9020delG | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78563506 | ||||||
| chr4:78563526 | ACGT | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.15+9040_15+9042del others(3): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78563526 | ||||||
| chr4:78563531 | T | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.15+9043T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563531 | |||||||
| chr4:78563548 | A | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0132 |
5 | NA18978.hp2 NA18979.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+9060A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563548 | |||||||
| chr4:78563564 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.15+9076G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563564 | |||||||
| chr4:78563731 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0266 a0001c0001t0001g0276 others(1): Show |
4 | HG02647.hp1 HG03041.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9243G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78563731 | |||||||
| chr4:78564536 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.16-8644G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78564536 | |||||||
| chr4:78564722 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(105): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.16-8458G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78564722 | |||||||
| chr4:78564991 | AT | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(109): Show |
135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.16-8169delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78564991 | ||||||
| chr4:78564991 | ATT | A | 25 | a0001c0001t0003g0017 a0001c0001t0004g0086 a0001c0001t0004g0145 others(22): Show |
27 | HG00735.hp1 HG01891.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.16-8170_16-8169del others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78564991 | ||||||
| chr4:78564991 | ATTT | A | 12 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0004g0035 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-8171_16-8169del others(3): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78564991 | ||||||
| chr4:78565146 | A | T | 1 | a0001c0001t0004g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.16-8034A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565146 | |||||||
| chr4:78565178 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.16-8002G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565178 | |||||||
| chr4:78565264 | G | A | 5 | a0001c0001t0001g0262 a0001c0001t0001g0266 a0001c0001t0001g0276 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-7916G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565264 | |||||||
| chr4:78565510 | G | T | 3 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 |
3 | HG00323.hp1 HG01106.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.16-7670G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565510 | |||||||
| chr4:78565540 | C | T | 2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.16-7640C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565540 | |||||||
| chr4:78565610 | C | T | 13 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0002g0066 others(10): Show |
13 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.16-7570C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565610 | |||||||
| chr4:78565680 | C | T | 1 | a0001c0001t0003g0119 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.16-7500C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565680 | |||||||
| chr4:78565906 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(195): Show |
229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.16-7274A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78565906 | |||||||
| chr4:78566052 | T | G | 10 | a0001c0001t0002g0278 a0001c0001t0004g0145 a0001c0001t0004g0146 others(7): Show |
11 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.16-7128T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566052 | |||||||
| chr4:78566054 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.16-7126A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566054 | |||||||
| chr4:78566156 | T | A | 1 | a0001c0001t0002g0047 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.16-7024T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566156 | |||||||
| chr4:78566440 | A | AATACT | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(188): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.16-6721_16-6717dup others(5): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78566440 | ||||||
| chr4:78566440 | A | AATACTAT others(3): Show |
6 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0001g0075 others(3): Show |
6 | HG02280.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-6726_16-6717dup others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78566440 | ||||||
| chr4:78566441 | A | G | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0002t0001g0087 |
3 | HG02572.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16-6739A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566441 | |||||||
| chr4:78566488 | C | CA | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.16-6678dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78566488 | ||||||
| chr4:78566712 | A | G | 2 | a0001c0001t0003g0017 a0004c0010t0004g0155 |
3 | HG00735.hp1 HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.16-6468A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566712 | |||||||
| chr4:78566847 | A | T | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-6333A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566847 | |||||||
| chr4:78566901 | A | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(100): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.16-6279A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78566901 | |||||||
| chr4:78567036 | C | T | 1 | a0001c0002t0006g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.16-6144C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567036 | |||||||
| chr4:78567116 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(190): Show |
224 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.16-6064G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567116 | |||||||
| chr4:78567257 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.16-5923T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567257 | |||||||
| chr4:78567264 | A | G | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.16-5916A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567264 | |||||||
| chr4:78567306 | A | T | 65 | a0001c0001t0001g0085 a0001c0001t0001g0133 a0001c0001t0001g0171 others(62): Show |
72 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.16-5874A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567306 | |||||||
| chr4:78567330 | C | G | 1 | a0001c0001t0002g0069 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16-5850C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567330 | |||||||
| chr4:78567359 | G | A | 1 | a0001c0001t0003g0169 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.16-5821G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567359 | |||||||
| chr4:78567411 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-5769C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567411 | |||||||
| chr4:78567472 | G | A | 18 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0004g0035 others(15): Show |
18 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.16-5708G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567472 | |||||||
| chr4:78567488 | CAT | C | 7 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(4): Show |
7 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-5691_16-5690del others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567488 | |||||||
| chr4:78567564 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.16-5616A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567564 | |||||||
| chr4:78567950 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.16-5230C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78567950 | |||||||
| chr4:78568000 | C | G | 9 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(6): Show |
9 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-5180C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568000 | |||||||
| chr4:78568070 | A | ATC | 8 | a0001c0001t0002g0072 a0001c0001t0002g0278 a0003c0004t0002g0082 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-5108_16-5107dup others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 78568070 | ||||||
| chr4:78568395 | G | A | 10 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0002g0066 others(7): Show |
10 | HG02145.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.16-4785G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568395 | |||||||
| chr4:78568671 | C | A | 1 | a0001c0002t0003g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.16-4509C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568671 | |||||||
| chr4:78568685 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.16-4495A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568685 | |||||||
| chr4:78568970 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.16-4210C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568970 | |||||||
| chr4:78568985 | T | A | 10 | a0001c0002t0001g0064 a0001c0002t0001g0073 a0001c0002t0001g0074 others(7): Show |
10 | HG02109.hp2 HG02280.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.16-4195T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78568985 | |||||||
| chr4:78569042 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.16-4138C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569042 | |||||||
| chr4:78569049 | A | G | 8 | a0001c0001t0002g0072 a0001c0001t0002g0278 a0003c0004t0002g0082 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-4131A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569049 | |||||||
| chr4:78569215 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.16-3965A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569215 | |||||||
| chr4:78569222 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0004g0086 a0001c0001t0004g0145 others(1): Show |
5 | HG00735.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-3958T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569222 | |||||||
| chr4:78569313 | C | T | 7 | a0001c0001t0002g0072 a0001c0001t0002g0278 a0003c0004t0002g0082 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-3867C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569313 | |||||||
| chr4:78569314 | G | A | 2 | a0001c0001t0001g0223 a0001c0011t0008g0084 |
2 | HG01175.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-3866G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569314 | |||||||
| chr4:78569711 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0163 a0004c0010t0004g0155 |
3 | HG01891.hp2 NA18944.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.16-3469C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569711 | |||||||
| chr4:78569767 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-3413A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78569767 | |||||||
| chr4:78570108 | C | G | 22 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(19): Show |
22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.16-3072C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570108 | |||||||
| chr4:78570162 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.16-3018A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570162 | |||||||
| chr4:78570697 | T | C | 1 | a0001c0001t0004g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.16-2483T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570697 | |||||||
| chr4:78570754 | T | C | 4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2426T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570754 | |||||||
| chr4:78570772 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.16-2408T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570772 | |||||||
| chr4:78570778 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16-2402G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78570778 | |||||||
| chr4:78571022 | T | C | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-2158T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571022 | |||||||
| chr4:78571253 | C | G | 1 | a0001c0001t0007g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.16-1927C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571253 | |||||||
| chr4:78571270 | G | T | 3 | a0001c0001t0003g0017 a0001c0001t0004g0145 a0001c0001t0004g0146 |
4 | HG00735.hp1 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-1910G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571270 | |||||||
| chr4:78571299 | C | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0132 a0001c0001t0001g0195 |
4 | NA18979.hp1 NA18998.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-1881C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571299 | |||||||
| chr4:78571496 | G | C | 1 | a0001c0001t0002g0123 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.16-1684G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571496 | |||||||
| chr4:78571634 | A | G | 1 | a0003c0004t0006g0083 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.16-1546A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571634 | |||||||
| chr4:78571794 | A | G | 8 | a0001c0001t0002g0072 a0001c0001t0002g0278 a0003c0004t0002g0082 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-1386A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78571794 | |||||||
| chr4:78572173 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-1007T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572173 | |||||||
| chr4:78572689 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(80): Show |
100 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.16-491G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572689 | |||||||
| chr4:78572690 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.16-490G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572690 | |||||||
| chr4:78572692 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.16-488C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572692 | |||||||
| chr4:78572771 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-409G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78572771 | |||||||
| chr4:78573153 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-27A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 2/12 | chr4 | 78573153 | |||||||
| chr4:78573276 | T | C | 64 | a0001c0001t0001g0133 a0001c0001t0001g0158 a0001c0001t0001g0177 others(61): Show |
72 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.103+9T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573276 | |||||||
| chr4:78573291 | T | G | 1 | a0001c0001t0003g0224 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.103+24T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573291 | |||||||
| chr4:78573392 | G | C | 4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+125G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573392 | |||||||
| chr4:78573511 | C | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0249 |
2 | HG00642.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.103+244C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573511 | |||||||
| chr4:78573652 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.103+385G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573652 | |||||||
| chr4:78573734 | G | T | 1 | a0001c0001t0003g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103+467G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573734 | |||||||
| chr4:78573864 | G | A | 1 | a0001c0001t0003g0174 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.103+597G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78573864 | |||||||
| chr4:78574027 | T | A | 11 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0219 others(8): Show |
13 | NA18952.hp2 NA18960.hp2 NA18968.hp1 others(10): Show |
intron_variant | MODIFIER | c.103+760T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78574027 | |||||||
| chr4:78574155 | C | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.103+888C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78574155 | |||||||
| chr4:78574802 | A | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(159): Show |
190 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.103+1535A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78574802 | |||||||
| chr4:78574904 | C | T | 1 | a0001c0012t0001g0279 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103+1637C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78574904 | |||||||
| chr4:78575014 | C | A | 1 | a0001c0001t0002g0101 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.103+1747C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575014 | |||||||
| chr4:78575240 | T | A | 1 | a0001c0001t0003g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.103+1973T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575240 | |||||||
| chr4:78575325 | G | A | 22 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(19): Show |
22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.103+2058G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575325 | |||||||
| chr4:78575334 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.103+2067G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575334 | |||||||
| chr4:78575399 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.103+2132G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575399 | |||||||
| chr4:78575443 | C | T | 12 | a0001c0001t0003g0017 a0001c0001t0004g0086 a0001c0001t0004g0145 others(9): Show |
14 | HG00735.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.103+2176C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575443 | |||||||
| chr4:78575444 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.103+2177G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575444 | |||||||
| chr4:78575556 | T | TG | 43 | a0001c0001t0001g0037 a0001c0001t0002g0072 a0001c0001t0002g0278 others(40): Show |
45 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.103+2289_103+2290i others(3): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575556 | |||||||
| chr4:78575674 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.103+2407G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575674 | |||||||
| chr4:78575681 | G | T | 6 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+2414G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575681 | |||||||
| chr4:78575827 | T | C | 1 | a0001c0001t0004g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103+2560T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78575827 | |||||||
| chr4:78576085 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0004g0055 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+2818G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576085 | |||||||
| chr4:78576191 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.104-2836A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576191 | |||||||
| chr4:78576507 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0105 others(6): Show |
11 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.104-2520C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576507 | |||||||
| chr4:78576572 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.104-2455T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576572 | |||||||
| chr4:78576575 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0214 |
2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.104-2452A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576575 | |||||||
| chr4:78576583 | C | A | 6 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-2444C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576583 | |||||||
| chr4:78576598 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.104-2429G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576598 | |||||||
| chr4:78576631 | T | A | 2 | a0001c0001t0003g0048 a0001c0001t0007g0152 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.104-2396T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576631 | |||||||
| chr4:78576713 | C | T | 4 | a0001c0002t0006g0277 a0001c0011t0008g0084 a0002c0003t0006g0011 others(1): Show |
5 | HG02258.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2314C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576713 | |||||||
| chr4:78576734 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.104-2293G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576734 | |||||||
| chr4:78576740 | G | T | 4 | a0001c0002t0006g0277 a0001c0011t0008g0084 a0002c0003t0006g0011 others(1): Show |
5 | HG02258.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2287G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576740 | |||||||
| chr4:78576793 | G | A | 5 | a0001c0001t0001g0056 a0001c0001t0003g0089 a0001c0001t0003g0090 others(2): Show |
5 | HG01109.hp2 HG03704.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2234G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78576793 | |||||||
| chr4:78577030 | A | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0196 a0001c0001t0001g0207 others(4): Show |
7 | HG00621.hp2 HG02056.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-1997A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577030 | |||||||
| chr4:78577242 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.104-1785C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577242 | |||||||
| chr4:78577267 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.104-1760T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577267 | |||||||
| chr4:78577367 | A | G | 44 | a0001c0001t0001g0037 a0001c0001t0002g0072 a0001c0001t0002g0278 others(41): Show |
46 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.104-1660A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577367 | |||||||
| chr4:78577814 | G | A | 4 | a0001c0002t0006g0277 a0001c0011t0008g0084 a0002c0003t0006g0011 others(1): Show |
5 | HG02258.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-1213G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577814 | |||||||
| chr4:78577934 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(158): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.104-1093C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577934 | |||||||
| chr4:78577968 | T | A | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104-1059T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78577968 | |||||||
| chr4:78578000 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.104-1027C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578000 | |||||||
| chr4:78578105 | C | T | 22 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(19): Show |
22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.104-922C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578105 | |||||||
| chr4:78578121 | T | TA | 6 | a0001c0001t0001g0259 a0001c0001t0002g0010 a0001c0001t0002g0067 others(3): Show |
7 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-896dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578121 | ||||||
| chr4:78578266 | A | G | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104-761A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578266 | |||||||
| chr4:78578282 | A | G | 40 | a0001c0001t0001g0037 a0001c0001t0002g0072 a0001c0001t0002g0278 others(37): Show |
42 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.104-745A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578282 | |||||||
| chr4:78578298 | C | CGA | 9 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0129 others(6): Show |
9 | HG02055.hp2 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-698_104-697dup others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGA | 12 | a0001c0001t0001g0012 a0001c0001t0001g0126 a0001c0001t0002g0002 others(9): Show |
14 | HG00733.hp1 HG01175.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.104-700_104-697dup others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGA | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0056 others(7): Show |
10 | HG01070.hp2 HG01109.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-702_104-697dup others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(1): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0028 others(7): Show |
10 | HG00280.hp2 HG00673.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-704_104-697dup others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(3): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0001g0228 others(4): Show |
7 | HG00140.hp2 HG00642.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-706_104-697dup others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(5): Show |
21 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(18): Show |
26 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.104-708_104-697dup others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(7): Show |
16 | a0001c0001t0001g0131 a0001c0001t0001g0171 a0001c0001t0001g0213 others(13): Show |
16 | HG01099.hp2 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.104-710_104-697dup others(14): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(9): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0026 others(9): Show |
14 | HG00408.hp2 HG02615.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-712_104-697dup others(16): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(11): Show |
21 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
24 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.104-714_104-697dup others(18): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(13): Show |
4 | a0001c0001t0001g0057 a0001c0001t0001g0207 a0001c0001t0002g0287 others(1): Show |
4 | HG02056.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-716_104-697dup others(20): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(15): Show |
4 | a0001c0001t0002g0199 a0001c0001t0002g0201 a0001c0001t0002g0202 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-718_104-697dup others(22): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGAG others(19): Show |
1 | a0001c0001t0005g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.104-722_104-697dup others(26): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGCG others(3): Show |
1 | a0001c0001t0003g0017 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.104-724_104-723ins others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGCG others(7): Show |
1 | a0001c0001t0003g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104-724_104-723ins others(14): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGCG others(11): Show |
1 | a0001c0001t0004g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-724_104-723ins others(18): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGTG others(5): Show |
6 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0219 others(3): Show |
6 | HG04228.hp1 NA18952.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGTG others(9): Show |
34 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0001g0194 others(31): Show |
38 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(16): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGTG others(11): Show |
7 | a0001c0001t0001g0133 a0001c0001t0001g0190 a0001c0001t0003g0018 others(4): Show |
7 | HG02074.hp1 NA18612.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(18): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | C | CGAGAGTG others(13): Show |
3 | a0001c0001t0003g0007 a0001c0001t0003g0255 a0001c0001t0003g0256 |
4 | NA18967.hp1 NA18970.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(20): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | CGA | C | 6 | a0001c0002t0006g0277 a0003c0004t0002g0082 a0003c0004t0004g0286 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-698_104-697del others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | CGAGA | C | 5 | a0001c0001t0002g0161 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG02258.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-700_104-697del others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | CGAGAGAG others(3): Show |
C | 1 | a0001c0002t0003g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.104-706_104-697del others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578298 | CGAGAGAG others(5): Show |
C | 1 | a0001c0001t0003g0288 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.104-708_104-697del others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578298 | ||||||
| chr4:78578300 | A | AGAGC | 18 | a0001c0002t0001g0032 a0001c0002t0001g0051 a0001c0002t0001g0053 others(15): Show |
18 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.104-724_104-723ins others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578300 | ||||||
| chr4:78578302 | A | T | 1 | a0001c0011t0008g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.104-725A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578302 | |||||||
| chr4:78578304 | A | C | 3 | a0001c0001t0002g0072 a0001c0001t0002g0278 a0001c0002t0003g0062 |
3 | HG02559.hp2 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.104-723A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578304 | |||||||
| chr4:78578304 | A | T | 4 | a0001c0001t0003g0118 a0001c0001t0003g0138 a0001c0001t0003g0186 others(1): Show |
4 | HG00544.hp1 HG01106.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-723A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578304 | |||||||
| chr4:78578306 | A | C | 1 | a0005c0005t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.104-721A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578306 | |||||||
| chr4:78578308 | A | C | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.104-719A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578308 | |||||||
| chr4:78578314 | A | C | 1 | a0001c0002t0003g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.104-713A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578314 | |||||||
| chr4:78578330 | A | AGAGAGAG others(2): Show |
4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0258 others(1): Show |
4 | HG01168.hp2 HG01255.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-697_104-696ins others(9): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | |||||||
| chr4:78578330 | A | AGAGAGAG others(6): Show |
7 | a0001c0001t0001g0173 a0001c0001t0001g0217 a0001c0001t0001g0234 others(4): Show |
7 | HG00408.hp1 HG00558.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-697_104-696ins others(13): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | |||||||
| chr4:78578330 | A | AGAGAGAG others(8): Show |
1 | a0001c0001t0001g0235 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.104-697_104-696ins others(15): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | |||||||
| chr4:78578330 | A | AGAGAGAG others(10): Show |
6 | a0001c0001t0001g0153 a0001c0001t0001g0195 a0001c0001t0003g0118 others(3): Show |
6 | HG00544.hp1 HG01106.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-697_104-696ins others(17): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | |||||||
| chr4:78578330 | A | AGAGAGAG others(12): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0276 |
2 | HG06807.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.104-697_104-696ins others(19): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | |||||||
| chr4:78578330 | A | AGAGAGAG others(14): Show |
2 | a0001c0001t0001g0106 a0001c0001t0002g0200 |
2 | HG01243.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.104-697_104-696ins others(21): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578330 | |||||||
| chr4:78578345 | G | C | 1 | a0001c0001t0005g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.104-682G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578345 | |||||||
| chr4:78578362 | A | AGAGGGAG others(9): Show |
39 | a0001c0001t0001g0037 a0001c0001t0002g0072 a0001c0001t0003g0017 others(36): Show |
41 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.104-655_104-654ins others(16): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578362 | ||||||
| chr4:78578467 | G | T | 4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-560G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578467 | |||||||
| chr4:78578473 | G | T | 1 | a0001c0002t0003g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.104-554G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578473 | |||||||
| chr4:78578533 | G | A | 1 | a0001c0002t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-494G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578533 | |||||||
| chr4:78578702 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.104-325C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578702 | |||||||
| chr4:78578720 | A | T | 1 | a0001c0001t0006g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.104-307A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578720 | |||||||
| chr4:78578722 | A | G | 10 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(7): Show |
11 | HG02258.hp1 HG02622.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.104-305A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578722 | |||||||
| chr4:78578753 | G | A | 22 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(19): Show |
22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.104-274G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578753 | |||||||
| chr4:78578768 | A | C | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104-259A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578768 | |||||||
| chr4:78578825 | CT | C | 40 | a0001c0001t0001g0037 a0001c0001t0002g0072 a0001c0001t0002g0179 others(37): Show |
42 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.104-193delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578825 | ||||||
| chr4:78578834 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(158): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.104-193T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | chr4 | 78578834 | |||||||
| chr4:78578852 | A | AAAAT | 31 | a0001c0001t0001g0057 a0001c0001t0001g0091 a0001c0001t0001g0093 others(28): Show |
35 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.104-139_104-136dup others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | ||||||
| chr4:78578852 | A | AAAATAAA others(1): Show |
67 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0180 others(64): Show |
75 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.104-143_104-136dup others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | ||||||
| chr4:78578852 | A | AAAATAAA others(5): Show |
4 | a0001c0001t0001g0285 a0001c0001t0002g0066 a0001c0001t0004g0055 others(1): Show |
4 | HG02717.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-147_104-136dup others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | ||||||
| chr4:78578852 | A | AAAATAAA others(9): Show |
1 | a0001c0001t0005g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.104-151_104-136dup others(16): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | ||||||
| chr4:78578852 | AAAATAAA others(1): Show |
A | 31 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(28): Show |
32 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.104-143_104-136del others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 78578852 | ||||||
| chr4:78579192 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+71G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579192 | |||||||
| chr4:78579366 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.198+245C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579366 | |||||||
| chr4:78579367 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.198+246A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579367 | |||||||
| chr4:78579464 | C | G | 22 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(19): Show |
22 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.198+343C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579464 | |||||||
| chr4:78579723 | G | A | 4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+602G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579723 | |||||||
| chr4:78579754 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.198+633C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579754 | |||||||
| chr4:78579868 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.198+747G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579868 | |||||||
| chr4:78579920 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.198+799G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579920 | |||||||
| chr4:78579931 | C | A | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.198+810C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579931 | |||||||
| chr4:78579955 | G | A | 1 | a0001c0001t0003g0118 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.198+834G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78579955 | |||||||
| chr4:78580145 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.198+1024G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580145 | |||||||
| chr4:78580349 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.198+1228G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580349 | |||||||
| chr4:78580408 | G | A | 3 | a0001c0001t0003g0017 a0001c0001t0004g0145 a0001c0001t0004g0146 |
4 | HG00735.hp1 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+1287G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580408 | |||||||
| chr4:78580586 | G | C | 23 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.198+1465G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580586 | |||||||
| chr4:78580591 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.198+1470A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580591 | |||||||
| chr4:78580600 | A | G | 6 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0002c0003t0004g0060 others(3): Show |
7 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+1479A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580600 | |||||||
| chr4:78580705 | C | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0132 others(1): Show |
6 | NA18978.hp2 NA18979.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-1472C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580705 | |||||||
| chr4:78580866 | A | G | 1 | a0001c0001t0002g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-1311A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580866 | |||||||
| chr4:78580871 | G | A | 47 | a0001c0001t0001g0037 a0001c0001t0002g0065 a0001c0001t0002g0066 others(44): Show |
49 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.199-1306G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580871 | |||||||
| chr4:78580888 | A | T | 25 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(22): Show |
25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.199-1289A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580888 | |||||||
| chr4:78580928 | T | G | 3 | a0001c0001t0002g0204 a0001c0001t0004g0151 a0002c0003t0004g0149 |
3 | HG02809.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-1249T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78580928 | |||||||
| chr4:78581278 | C | T | 23 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-899C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581278 | |||||||
| chr4:78581287 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(157): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.199-890G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581287 | |||||||
| chr4:78581343 | G | C | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.199-834G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581343 | |||||||
| chr4:78581403 | G | A | 1 | a0001c0001t0004g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-774G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581403 | |||||||
| chr4:78581415 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(205): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.199-762A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581415 | |||||||
| chr4:78581616 | T | C | 1 | a0001c0002t0006g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.199-561T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581616 | |||||||
| chr4:78581818 | T | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(85): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.199-359T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581818 | |||||||
| chr4:78581875 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.199-302A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581875 | |||||||
| chr4:78581942 | A | G | 23 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-235A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78581942 | |||||||
| chr4:78582076 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(170): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.199-101T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 4/12 | chr4 | 78582076 | |||||||
| chr4:78582416 | G | A | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.312+126G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582416 | |||||||
| chr4:78582497 | T | C | 2 | a0001c0001t0004g0070 a0001c0001t0004g0071 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.312+207T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582497 | |||||||
| chr4:78582580 | A | G | 8 | a0001c0001t0003g0017 a0001c0001t0004g0145 a0001c0001t0004g0146 others(5): Show |
9 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+290A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582580 | |||||||
| chr4:78582635 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.312+345A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582635 | |||||||
| chr4:78582784 | A | G | 25 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(22): Show |
25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.312+494A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582784 | |||||||
| chr4:78582967 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
227 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.312+677G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78582967 | |||||||
| chr4:78583098 | G | A | 3 | a0001c0001t0003g0017 a0001c0001t0004g0145 a0001c0001t0004g0146 |
4 | HG00735.hp1 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+808G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583098 | |||||||
| chr4:78583158 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.312+868G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583158 | |||||||
| chr4:78583175 | C | G | 1 | a0005c0005t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.312+885C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583175 | |||||||
| chr4:78583182 | TA | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.312+902delA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 78583182 | ||||||
| chr4:78583216 | C | A | 2 | a0001c0001t0002g0072 a0005c0005t0003g0080 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.312+926C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583216 | |||||||
| chr4:78583287 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.312+997A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583287 | |||||||
| chr4:78583462 | A | C | 1 | a0002c0003t0004g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.312+1172A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583462 | |||||||
| chr4:78583536 | A | C | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.312+1246A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583536 | |||||||
| chr4:78583550 | G | A | 1 | a0001c0001t0004g0265 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.312+1260G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583550 | |||||||
| chr4:78583563 | A | G | 25 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(22): Show |
25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.312+1273A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583563 | |||||||
| chr4:78583613 | G | GA | 7 | a0001c0001t0001g0236 a0001c0001t0002g0096 a0001c0001t0003g0019 others(4): Show |
8 | HG00544.hp1 HG01952.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+1338dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 78583613 | ||||||
| chr4:78583626 | A | G | 25 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(22): Show |
25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.312+1336A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583626 | |||||||
| chr4:78583756 | T | G | 4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+1466T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78583756 | |||||||
| chr4:78584064 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0193 |
3 | NA18968.hp1 NA18978.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.312+1774G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584064 | |||||||
| chr4:78584111 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.312+1821A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584111 | |||||||
| chr4:78584131 | C | T | 9 | a0001c0001t0002g0278 a0001c0001t0003g0017 a0001c0001t0004g0145 others(6): Show |
10 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.312+1841C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584131 | |||||||
| chr4:78584152 | G | T | 1 | a0001c0002t0001g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.312+1862G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584152 | |||||||
| chr4:78584163 | T | A | 9 | a0001c0002t0001g0064 a0001c0002t0001g0073 a0001c0002t0001g0074 others(6): Show |
9 | HG02109.hp2 HG02280.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+1873T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584163 | |||||||
| chr4:78584412 | G | A | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.313-1848G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584412 | |||||||
| chr4:78584420 | C | T | 3 | a0001c0001t0002g0043 a0001c0001t0002g0159 a0001c0001t0002g0191 |
3 | HG00673.hp2 HG02056.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.313-1840C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584420 | |||||||
| chr4:78584427 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.313-1833C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584427 | |||||||
| chr4:78584431 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.313-1829C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584431 | |||||||
| chr4:78584513 | T | G | 1 | a0005c0005t0003g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.313-1747T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584513 | |||||||
| chr4:78584618 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(195): Show |
228 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.313-1642T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584618 | |||||||
| chr4:78584730 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(157): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.313-1530T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584730 | |||||||
| chr4:78584784 | T | A | 25 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(22): Show |
25 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.313-1476T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584784 | |||||||
| chr4:78584814 | G | A | 14 | a0001c0001t0001g0037 a0001c0001t0002g0072 a0001c0001t0002g0278 others(11): Show |
14 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-1446G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584814 | |||||||
| chr4:78584828 | G | C | 1 | a0001c0002t0006g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.313-1432G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584828 | |||||||
| chr4:78584842 | C | T | 1 | a0001c0001t0003g0185 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.313-1418C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78584842 | |||||||
| chr4:78585041 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.313-1219G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585041 | |||||||
| chr4:78585268 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0163 |
2 | NA18944.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.313-992T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585268 | |||||||
| chr4:78585269 | C | A | 1 | a0001c0001t0002g0287 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.313-991C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585269 | |||||||
| chr4:78585380 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.313-880A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585380 | |||||||
| chr4:78585574 | C | G | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.313-686C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585574 | |||||||
| chr4:78585710 | G | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.313-550G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585710 | |||||||
| chr4:78585761 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0004g0070 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-499A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585761 | |||||||
| chr4:78585809 | A | T | 4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-451A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585809 | |||||||
| chr4:78585990 | A | G | 1 | a0001c0001t0004g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.313-270A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78585990 | |||||||
| chr4:78586257 | T | C | 1 | a0001c0001t0002g0004 | 3 | HG00140.hp1 HG01099.hp1 HG02257.hp2 |
splice_region_variant&intron_variant | LOW | c.313-3T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 5/12 | chr4 | 78586257 | |||||||
| chr4:78586431 | C | T | 4 | a0002c0003t0004g0060 a0002c0003t0004g0061 a0002c0003t0006g0011 others(1): Show |
5 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+81C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78586431 | |||||||
| chr4:78586681 | G | A | 1 | a0001c0001t0003g0017 | 2 | HG00735.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.403+331G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78586681 | |||||||
| chr4:78586681 | G | T | 5 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
5 | HG00597.hp2 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+331G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78586681 | |||||||
| chr4:78586956 | C | T | 8 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(5): Show |
8 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+606C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78586956 | |||||||
| chr4:78587059 | T | C | 1 | a0001c0001t0005g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.403+709T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587059 | |||||||
| chr4:78587087 | A | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.403+737A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587087 | |||||||
| chr4:78587218 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(157): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.403+868C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587218 | |||||||
| chr4:78587410 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.403+1060C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587410 | |||||||
| chr4:78587453 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(157): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.403+1103G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587453 | |||||||
| chr4:78587505 | C | T | 1 | a0005c0005t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.403+1155C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587505 | |||||||
| chr4:78587650 | G | A | 1 | a0001c0001t0003g0247 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.403+1300G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587650 | |||||||
| chr4:78587712 | C | T | 7 | a0001c0001t0001g0126 a0001c0001t0002g0013 a0001c0001t0002g0027 others(4): Show |
9 | HG00733.hp1 HG01070.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+1362C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587712 | |||||||
| chr4:78587732 | C | A | 1 | a0001c0002t0006g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.403+1382C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587732 | |||||||
| chr4:78587732 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(178): Show |
211 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.403+1382C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587732 | |||||||
| chr4:78587818 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.403+1468G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587818 | |||||||
| chr4:78587821 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(170): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.403+1471C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587821 | |||||||
| chr4:78587853 | G | A | 1 | a0001c0001t0003g0118 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.403+1503G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78587853 | |||||||
| chr4:78588107 | T | C | 1 | a0001c0001t0002g0154 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.403+1757T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588107 | |||||||
| chr4:78588220 | C | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(178): Show |
211 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.403+1870C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588220 | |||||||
| chr4:78588669 | A | G | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.403+2319A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588669 | |||||||
| chr4:78588927 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.403+2577T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588927 | |||||||
| chr4:78588986 | G | A | 23 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.404-2558G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78588986 | |||||||
| chr4:78589103 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.404-2441C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589103 | |||||||
| chr4:78589142 | C | A | 1 | a0001c0001t0002g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.404-2402C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589142 | |||||||
| chr4:78589182 | C | T | 1 | a0001c0001t0003g0127 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.404-2362C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589182 | |||||||
| chr4:78589212 | C | T | 1 | a0001c0002t0006g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.404-2332C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589212 | |||||||
| chr4:78589213 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
227 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.404-2331A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589213 | |||||||
| chr4:78589304 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(192): Show |
225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.404-2240A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589304 | |||||||
| chr4:78589310 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0005g0036 others(1): Show |
4 | HG02886.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-2234C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589310 | |||||||
| chr4:78589324 | A | G | 23 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0051 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.404-2220A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589324 | |||||||
| chr4:78589343 | G | T | 2 | a0001c0001t0001g0126 a0001c0002t0001g0281 |
2 | HG02040.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.404-2201G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589343 | |||||||
| chr4:78589359 | G | A | 1 | a0001c0002t0006g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.404-2185G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589359 | |||||||
| chr4:78589417 | A | G | 24 | a0001c0001t0002g0278 a0001c0002t0001g0032 a0001c0002t0001g0049 others(21): Show |
24 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-2127A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589417 | |||||||
| chr4:78589517 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.404-2027G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589517 | |||||||
| chr4:78589677 | G | A | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404-1867G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589677 | |||||||
| chr4:78589801 | A | G | 1 | a0001c0001t0002g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.404-1743A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589801 | |||||||
| chr4:78589819 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
236 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.404-1725T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589819 | |||||||
| chr4:78589877 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.404-1667C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589877 | |||||||
| chr4:78589900 | G | A | 24 | a0001c0001t0002g0278 a0001c0002t0001g0032 a0001c0002t0001g0049 others(21): Show |
24 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-1644G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78589900 | |||||||
| chr4:78590163 | G | C | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404-1381G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590163 | |||||||
| chr4:78590209 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(175): Show |
208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.404-1335T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590209 | |||||||
| chr4:78590319 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0120 a0001c0001t0001g0262 |
4 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1225T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590319 | |||||||
| chr4:78590322 | A | T | 2 | a0001c0001t0002g0072 a0005c0005t0003g0080 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.404-1222A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590322 | |||||||
| chr4:78590346 | A | G | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.404-1198A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590346 | |||||||
| chr4:78590385 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0004g0035 a0001c0001t0005g0036 others(1): Show |
4 | HG02886.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1159A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590385 | |||||||
| chr4:78590400 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.404-1144G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590400 | |||||||
| chr4:78590504 | C | A | 1 | a0001c0001t0003g0168 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.404-1040C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590504 | |||||||
| chr4:78590667 | G | A | 4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.404-877G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590667 | |||||||
| chr4:78590762 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.404-782T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590762 | |||||||
| chr4:78590777 | T | TAAGATTA others(321): Show |
1 | a0001c0002t0001g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.404-756_404-755ins others(328): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | ||||||
| chr4:78590777 | T | TAAGATTA others(318): Show |
1 | a0001c0002t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.404-756_404-755ins others(325): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | ||||||
| chr4:78590777 | T | TAAGATTA others(319): Show |
2 | a0001c0002t0003g0062 a0001c0012t0001g0279 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.404-756_404-755ins others(326): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | ||||||
| chr4:78590777 | T | TAAGATTA others(320): Show |
3 | a0001c0002t0003g0050 a0001c0002t0004g0148 a0001c0002t0006g0147 |
3 | HG01891.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.404-756_404-755ins others(327): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | ||||||
| chr4:78590777 | T | TAAGATTA others(321): Show |
11 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0053 others(8): Show |
11 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.404-756_404-755ins others(328): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | ||||||
| chr4:78590777 | T | TAAGATTA others(322): Show |
3 | a0001c0002t0001g0073 a0001c0002t0001g0076 a0001c0002t0001g0087 |
3 | HG03471.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.404-756_404-755ins others(329): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | ||||||
| chr4:78590777 | T | TAAGATTA others(323): Show |
2 | a0001c0002t0001g0075 a0001c0002t0001g0282 |
2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.404-756_404-755ins others(330): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 78590777 | ||||||
| chr4:78590832 | A | AAGCCACT others(2): Show |
6 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0053 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-712_404-711ins others(9): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590832 | |||||||
| chr4:78590833 | G | A | 6 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0053 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-711G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590833 | |||||||
| chr4:78590835 | A | G | 6 | a0001c0002t0001g0032 a0001c0002t0001g0049 a0001c0002t0001g0053 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-709A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590835 | |||||||
| chr4:78590916 | T | A | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404-628T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590916 | |||||||
| chr4:78590920 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.404-624A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590920 | |||||||
| chr4:78590946 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.404-598T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 6/12 | chr4 | 78590946 | |||||||
| chr4:78591646 | T | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(156): Show |
187 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.483+23T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591646 | |||||||
| chr4:78591702 | C | G | 1 | a0001c0001t0002g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.483+79C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591702 | |||||||
| chr4:78591853 | T | C | 2 | a0001c0002t0006g0277 a0001c0011t0008g0084 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.483+230T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591853 | |||||||
| chr4:78591962 | G | A | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483+339G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591962 | |||||||
| chr4:78591975 | C | A | 1 | a0001c0011t0008g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.483+352C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78591975 | |||||||
| chr4:78592061 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(115): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.483+438A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592061 | |||||||
| chr4:78592217 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(193): Show |
226 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.483+594T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592217 | |||||||
| chr4:78592230 | A | G | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483+607A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592230 | |||||||
| chr4:78592288 | A | G | 5 | a0001c0001t0002g0278 a0003c0004t0002g0082 a0003c0004t0004g0286 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+665A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592288 | |||||||
| chr4:78592320 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.483+697A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592320 | |||||||
| chr4:78592410 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.483+787C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592410 | |||||||
| chr4:78592428 | G | A | 6 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+805G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592428 | |||||||
| chr4:78592453 | A | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
227 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.483+830A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592453 | |||||||
| chr4:78592539 | A | G | 22 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(19): Show |
22 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+916A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592539 | |||||||
| chr4:78592612 | T | C | 3 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0092 |
3 | HG03704.hp2 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.483+989T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592612 | |||||||
| chr4:78592820 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.483+1197A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592820 | |||||||
| chr4:78592859 | G | A | 2 | a0001c0001t0003g0017 a0004c0010t0004g0155 |
3 | HG00735.hp1 HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.483+1236G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78592859 | |||||||
| chr4:78593020 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18979.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.483+1397A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593020 | |||||||
| chr4:78593040 | G | A | 2 | a0001c0001t0002g0072 a0005c0005t0003g0080 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.483+1417G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593040 | |||||||
| chr4:78593112 | A | AACACAC | 3 | a0001c0001t0001g0026 a0001c0001t0001g0229 a0001c0001t0002g0246 |
4 | HG03710.hp1 NA18951.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+1489_483+1490i others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593112 | |||||||
| chr4:78593113 | C | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0229 a0001c0001t0002g0246 |
4 | HG03710.hp1 NA18951.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+1490C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593113 | |||||||
| chr4:78593113 | C | CCA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0037 others(27): Show |
33 | HG00423.hp1 HG00597.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.483+1528_483+1529d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593113 | C | CCACA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(115): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.483+1526_483+1529d others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593113 | C | CCACACA | 21 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(18): Show |
26 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.483+1524_483+1529d others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593113 | C | CCACACAC others(1): Show |
12 | a0001c0001t0001g0014 a0001c0001t0001g0091 a0001c0001t0001g0129 others(9): Show |
12 | HG00140.hp2 HG01099.hp1 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.483+1522_483+1529d others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593113 | C | CCACACAC others(3): Show |
2 | a0001c0001t0001g0106 a0001c0001t0002g0215 |
2 | HG02135.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.483+1520_483+1529d others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593113 | C | CCACACAC others(5): Show |
1 | a0001c0001t0001g0252 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.483+1518_483+1529d others(14): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593113 | CCA | C | 59 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0180 others(56): Show |
66 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.483+1528_483+1529d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593113 | CCACA | C | 15 | a0001c0001t0002g0039 a0001c0001t0003g0017 a0001c0001t0003g0020 others(12): Show |
17 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.483+1526_483+1529d others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593113 | CCACACA | C | 6 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+1524_483+1529d others(8): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593113 | ||||||
| chr4:78593151 | A | C | 6 | a0001c0001t0003g0017 a0001c0011t0008g0084 a0003c0004t0002g0082 others(3): Show |
7 | HG00735.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+1528A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593151 | |||||||
| chr4:78593186 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.483+1563G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593186 | |||||||
| chr4:78593224 | A | G | 1 | a0001c0001t0003g0257 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.483+1601A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593224 | |||||||
| chr4:78593250 | T | A | 22 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(19): Show |
22 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+1627T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593250 | |||||||
| chr4:78593251 | G | GA | 22 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(19): Show |
22 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+1628_483+1629i others(3): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593251 | |||||||
| chr4:78593263 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(124): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.483+1640T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593263 | |||||||
| chr4:78593264 | G | A | 1 | a0001c0001t0005g0245 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.483+1641G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593264 | |||||||
| chr4:78593340 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.483+1717T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593340 | |||||||
| chr4:78593400 | T | C | 30 | a0001c0001t0001g0276 a0001c0001t0004g0035 a0001c0001t0004g0070 others(27): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.483+1777T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593400 | |||||||
| chr4:78593449 | G | A | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0003g0089 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+1826G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593449 | |||||||
| chr4:78593454 | A | G | 1 | a0005c0005t0003g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.483+1831A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593454 | |||||||
| chr4:78593612 | C | T | 30 | a0001c0001t0001g0276 a0001c0001t0004g0035 a0001c0001t0004g0070 others(27): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-1769C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593612 | |||||||
| chr4:78593625 | C | CATT | 6 | a0001c0001t0002g0109 a0001c0001t0002g0141 a0001c0001t0002g0200 others(3): Show |
6 | HG01106.hp1 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-1731_484-1729d others(5): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593625 | ||||||
| chr4:78593625 | C | CATTATTA others(2): Show |
23 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.484-1737_484-1729d others(11): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593625 | ||||||
| chr4:78593625 | C | CATTATTA others(14): Show |
5 | a0002c0003t0004g0060 a0002c0003t0004g0061 a0002c0003t0004g0149 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-1749_484-1729d others(23): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593625 | ||||||
| chr4:78593763 | A | G | 21 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(18): Show |
21 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.484-1618A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593763 | |||||||
| chr4:78593774 | C | G | 67 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0180 others(64): Show |
75 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.484-1607C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593774 | |||||||
| chr4:78593795 | T | C | 30 | a0001c0001t0001g0276 a0001c0001t0004g0035 a0001c0001t0004g0070 others(27): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-1586T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593795 | |||||||
| chr4:78593798 | A | G | 39 | a0001c0001t0001g0276 a0001c0001t0003g0017 a0001c0001t0004g0035 others(36): Show |
40 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.484-1583A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593798 | |||||||
| chr4:78593803 | A | AT | 22 | a0001c0001t0001g0133 a0001c0001t0001g0144 a0001c0001t0001g0163 others(19): Show |
23 | HG00597.hp2 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.484-1552dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | ||||||
| chr4:78593803 | A | ATT | 15 | a0001c0001t0002g0248 a0001c0002t0001g0032 a0001c0002t0001g0049 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-1553_484-1552d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | ||||||
| chr4:78593803 | AT | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(97): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.484-1552delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | ||||||
| chr4:78593803 | ATT | A | 65 | a0001c0001t0001g0102 a0001c0001t0001g0130 a0001c0001t0001g0158 others(62): Show |
73 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.484-1553_484-1552d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | ||||||
| chr4:78593803 | ATTTTTTT others(6): Show |
A | 5 | a0001c0002t0004g0148 a0003c0004t0002g0082 a0003c0004t0004g0286 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-1564_484-1552d others(15): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78593803 | ||||||
| chr4:78593835 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.484-1546G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78593835 | |||||||
| chr4:78594159 | TCAGG | T | 30 | a0001c0001t0001g0276 a0001c0001t0004g0035 a0001c0001t0004g0070 others(27): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-1216_484-1213d others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78594159 | ||||||
| chr4:78594211 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.484-1170G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594211 | |||||||
| chr4:78594314 | G | GT | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(197): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.484-1064dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78594314 | ||||||
| chr4:78594462 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.484-919C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594462 | |||||||
| chr4:78594469 | C | G | 2 | a0001c0002t0006g0277 a0005c0005t0003g0080 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.484-912C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594469 | |||||||
| chr4:78594496 | A | C | 2 | a0001c0002t0006g0277 a0005c0005t0003g0080 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.484-885A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594496 | |||||||
| chr4:78594556 | A | G | 6 | a0001c0001t0003g0017 a0001c0011t0008g0084 a0003c0004t0002g0082 others(3): Show |
7 | HG00735.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-825A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594556 | |||||||
| chr4:78594570 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(197): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.484-811A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594570 | |||||||
| chr4:78594739 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.484-642G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594739 | |||||||
| chr4:78594851 | G | A | 2 | a0001c0001t0002g0287 a0005c0005t0003g0063 |
2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.484-530G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78594851 | |||||||
| chr4:78595045 | G | A | 2 | a0001c0001t0004g0055 a0001c0001t0005g0059 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.484-336G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595045 | |||||||
| chr4:78595051 | G | A | 30 | a0001c0001t0001g0276 a0001c0001t0004g0035 a0001c0001t0004g0070 others(27): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-330G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595051 | |||||||
| chr4:78595130 | A | C | 30 | a0001c0001t0001g0276 a0001c0001t0004g0035 a0001c0001t0004g0070 others(27): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.484-251A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595130 | |||||||
| chr4:78595141 | A | AATATAT | 7 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-231_484-226dup others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 78595141 | ||||||
| chr4:78595163 | C | T | 10 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(7): Show |
10 | HG02145.hp1 HG02723.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-218C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595163 | |||||||
| chr4:78595212 | C | A | 2 | a0001c0002t0001g0281 a0001c0002t0006g0147 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.484-169C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595212 | |||||||
| chr4:78595227 | G | T | 23 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(20): Show |
23 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.484-154G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595227 | |||||||
| chr4:78595233 | C | T | 1 | a0003c0004t0002g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.484-148C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595233 | |||||||
| chr4:78595273 | C | G | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.484-108C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595273 | |||||||
| chr4:78595291 | A | G | 4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-90A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 7/12 | chr4 | 78595291 | |||||||
| chr4:78595536 | T | TTTTC | 21 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(18): Show |
21 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.540+103_540+106dup others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 78595536 | ||||||
| chr4:78595540 | C | CT | 5 | a0001c0001t0003g0176 a0001c0002t0001g0281 a0001c0002t0006g0147 others(2): Show |
6 | HG01891.hp1 HG02258.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+116dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 78595540 | ||||||
| chr4:78595540 | C | CTTTTTT | 7 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+111_540+116dup others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 78595540 | ||||||
| chr4:78595540 | CT | C | 7 | a0001c0001t0001g0057 a0001c0001t0001g0285 a0001c0001t0004g0055 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+116delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 78595540 | ||||||
| chr4:78595900 | A | T | 7 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+13A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78595900 | |||||||
| chr4:78595956 | A | G | 7 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+69A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78595956 | |||||||
| chr4:78596152 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.634+265G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596152 | |||||||
| chr4:78596152 | G | T | 1 | a0001c0002t0001g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.634+265G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596152 | |||||||
| chr4:78596359 | T | C | 1 | a0001c0002t0004g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.634+472T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596359 | |||||||
| chr4:78596360 | C | T | 23 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(20): Show |
23 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.634+473C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596360 | |||||||
| chr4:78596389 | G | T | 1 | a0001c0012t0001g0279 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.634+502G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596389 | |||||||
| chr4:78596403 | T | C | 38 | a0001c0001t0001g0276 a0001c0001t0003g0017 a0001c0001t0004g0035 others(35): Show |
39 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.634+516T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596403 | |||||||
| chr4:78596461 | T | C | 30 | a0001c0001t0001g0276 a0001c0001t0004g0035 a0001c0001t0004g0070 others(27): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.634+574T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596461 | |||||||
| chr4:78596620 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0120 a0001c0001t0001g0262 |
4 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-699G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596620 | |||||||
| chr4:78596839 | A | G | 1 | a0001c0001t0005g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.635-480A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78596839 | |||||||
| chr4:78597058 | A | G | 7 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-261A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597058 | |||||||
| chr4:78597140 | T | C | 12 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(9): Show |
13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.635-179T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597140 | |||||||
| chr4:78597242 | A | G | 1 | a0001c0001t0005g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.635-77A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597242 | |||||||
| chr4:78597283 | C | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0105 others(6): Show |
11 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-36C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597283 | |||||||
| chr4:78597284 | G | A | 2 | a0001c0002t0001g0281 a0001c0002t0006g0147 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.635-35G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 9/12 | chr4 | 78597284 | |||||||
| chr4:78597425 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.730+11G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597425 | |||||||
| chr4:78597499 | CT | C | 2 | a0002c0003t0006g0011 a0002c0003t0006g0135 |
3 | HG02258.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.730+86delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597499 | |||||||
| chr4:78597693 | G | C | 23 | a0001c0001t0001g0276 a0001c0002t0001g0032 a0001c0002t0001g0049 others(20): Show |
23 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.730+279G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597693 | |||||||
| chr4:78597733 | C | T | 35 | a0001c0001t0001g0276 a0001c0001t0004g0035 a0001c0001t0004g0070 others(32): Show |
36 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(33): Show |
intron_variant | MODIFIER | c.730+319C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597733 | |||||||
| chr4:78597814 | A | G | 1 | a0001c0002t0006g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.730+400A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597814 | |||||||
| chr4:78597831 | C | T | 1 | a0001c0001t0003g0184 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.730+417C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597831 | |||||||
| chr4:78597983 | C | T | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG00597.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+569C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78597983 | |||||||
| chr4:78598046 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.730+632G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598046 | |||||||
| chr4:78598054 | A | G | 14 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(11): Show |
15 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.730+640A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598054 | |||||||
| chr4:78598070 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
9 | HG00558.hp2 NA18948.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.730+656C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598070 | |||||||
| chr4:78598071 | G | A | 2 | a0001c0002t0006g0277 a0005c0005t0003g0080 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.730+657G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598071 | |||||||
| chr4:78598148 | T | C | 2 | a0001c0002t0001g0077 a0001c0002t0001g0079 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.730+734T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598148 | |||||||
| chr4:78598178 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.730+764A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598178 | |||||||
| chr4:78598179 | C | CCA | 15 | a0001c0001t0002g0043 a0001c0001t0002g0072 a0001c0001t0002g0159 others(12): Show |
16 | HG00673.hp2 HG02056.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.730+792_730+793dup others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598179 | ||||||
| chr4:78598179 | C | CCACACAC others(3): Show |
4 | a0003c0004t0002g0082 a0003c0004t0004g0286 a0003c0004t0006g0081 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+784_730+793dup others(10): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598179 | ||||||
| chr4:78598179 | C | CCACACAC others(5): Show |
2 | a0001c0001t0003g0017 a0001c0011t0008g0084 |
3 | HG00735.hp1 HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.730+782_730+793dup others(12): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598179 | ||||||
| chr4:78598292 | C | CT | 22 | a0001c0001t0003g0017 a0001c0001t0004g0035 a0001c0001t0004g0070 others(19): Show |
24 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.730+890dupT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598292 | ||||||
| chr4:78598334 | C | G | 1 | a0001c0001t0003g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.730+920C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598334 | |||||||
| chr4:78598397 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.730+983C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598397 | |||||||
| chr4:78598480 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.730+1066G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598480 | |||||||
| chr4:78598500 | C | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(197): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.730+1086C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598500 | |||||||
| chr4:78598544 | CT | C | 22 | a0001c0001t0003g0017 a0001c0001t0004g0035 a0001c0001t0004g0070 others(19): Show |
24 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.730+1139delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78598544 | ||||||
| chr4:78598594 | T | C | 16 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(13): Show |
17 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.730+1180T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598594 | |||||||
| chr4:78598600 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0238 a0001c0001t0001g0241 |
3 | NA18999.hp1 NA19065.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.730+1186C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598600 | |||||||
| chr4:78598625 | C | T | 2 | a0001c0001t0003g0048 a0001c0001t0007g0152 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.730+1211C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598625 | |||||||
| chr4:78598689 | G | A | 1 | a0001c0002t0004g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.730+1275G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598689 | |||||||
| chr4:78598783 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.730+1369G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598783 | |||||||
| chr4:78598834 | CT | C | 3 | a0001c0001t0004g0035 a0001c0001t0005g0036 a0001c0001t0005g0058 |
3 | HG02886.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.730+1421delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598834 | |||||||
| chr4:78598901 | C | T | 3 | a0001c0001t0002g0042 a0001c0001t0002g0047 a0001c0001t0002g0160 |
3 | HG02074.hp2 HG02135.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.730+1487C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78598901 | |||||||
| chr4:78599012 | A | G | 2 | a0001c0002t0006g0277 a0005c0005t0003g0080 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.730+1598A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599012 | |||||||
| chr4:78599046 | C | A | 1 | a0001c0002t0004g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.730+1632C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599046 | |||||||
| chr4:78599160 | C | T | 43 | a0001c0001t0001g0276 a0001c0001t0003g0017 a0001c0001t0004g0035 others(40): Show |
45 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.730+1746C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599160 | |||||||
| chr4:78599161 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(84): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.730+1747T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599161 | |||||||
| chr4:78599178 | A | G | 9 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(6): Show |
9 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.730+1764A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599178 | |||||||
| chr4:78599221 | A | G | 2 | a0001c0002t0006g0277 a0005c0005t0003g0080 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.730+1807A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599221 | |||||||
| chr4:78599235 | C | T | 1 | a0001c0012t0001g0279 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.730+1821C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599235 | |||||||
| chr4:78599249 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.730+1835G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599249 | |||||||
| chr4:78599394 | C | T | 11 | a0001c0001t0004g0035 a0001c0001t0004g0070 a0001c0001t0004g0071 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.730+1980C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599394 | |||||||
| chr4:78599553 | C | G | 5 | a0002c0003t0004g0060 a0002c0003t0004g0061 a0002c0003t0004g0149 others(2): Show |
6 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1957C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599553 | |||||||
| chr4:78599624 | T | A | 5 | a0001c0001t0001g0056 a0001c0001t0003g0089 a0001c0001t0003g0090 others(2): Show |
5 | HG01109.hp2 HG03704.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-1886T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599624 | |||||||
| chr4:78599656 | G | A | 6 | a0001c0002t0001g0281 a0001c0002t0006g0147 a0001c0002t0006g0277 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1854G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599656 | |||||||
| chr4:78599744 | A | T | 42 | a0001c0001t0001g0276 a0001c0001t0003g0017 a0001c0001t0003g0089 others(39): Show |
44 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.731-1766A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599744 | |||||||
| chr4:78599808 | C | T | 9 | a0001c0002t0001g0064 a0001c0002t0001g0073 a0001c0002t0001g0074 others(6): Show |
9 | HG02109.hp2 HG02280.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.731-1702C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599808 | |||||||
| chr4:78599943 | T | C | 10 | a0001c0001t0003g0020 a0001c0001t0003g0166 a0001c0001t0003g0178 others(7): Show |
11 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(8): Show |
intron_variant | MODIFIER | c.731-1567T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78599943 | |||||||
| chr4:78600031 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0033 |
3 | HG01952.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.731-1479C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600031 | |||||||
| chr4:78600046 | G | T | 51 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0190 others(48): Show |
58 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.731-1464G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600046 | |||||||
| chr4:78600274 | G | A | 65 | a0001c0001t0001g0158 a0001c0001t0001g0243 a0001c0001t0002g0027 others(62): Show |
75 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.731-1236G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600274 | |||||||
| chr4:78600482 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.731-1028A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600482 | |||||||
| chr4:78600671 | G | A | 2 | a0001c0001t0004g0070 a0001c0001t0004g0071 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.731-839G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600671 | |||||||
| chr4:78600748 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.731-762C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600748 | |||||||
| chr4:78600825 | T | G | 1 | a0001c0001t0001g0239 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.731-685T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600825 | |||||||
| chr4:78600921 | G | T | 3 | a0001c0002t0006g0277 a0003c0004t0006g0081 a0003c0004t0006g0083 |
3 | HG02280.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.731-589G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600921 | |||||||
| chr4:78600936 | AT | A | 10 | a0001c0001t0002g0039 a0001c0001t0003g0017 a0001c0001t0003g0048 others(7): Show |
11 | HG00735.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.731-564delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 78600936 | ||||||
| chr4:78600967 | A | G | 7 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(4): Show |
8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-543A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600967 | |||||||
| chr4:78600997 | A | C | 7 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(4): Show |
8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-513A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78600997 | |||||||
| chr4:78601054 | T | C | 7 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(4): Show |
8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-456T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601054 | |||||||
| chr4:78601057 | C | T | 1 | a0001c0006t0001g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.731-453C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601057 | |||||||
| chr4:78601085 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.731-425G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601085 | |||||||
| chr4:78601132 | A | G | 4 | a0001c0001t0001g0259 a0001c0001t0002g0029 a0001c0001t0002g0215 others(1): Show |
5 | HG01358.hp2 HG01934.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-378A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601132 | |||||||
| chr4:78601360 | C | A | 1 | a0003c0004t0004g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.731-150C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601360 | |||||||
| chr4:78601370 | A | C | 2 | a0001c0001t0003g0169 a0001c0001t0003g0221 |
2 | NA18939.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.731-140A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601370 | |||||||
| chr4:78601415 | C | T | 3 | a0001c0002t0004g0148 a0005c0005t0003g0063 a0005c0005t0003g0080 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.731-95C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601415 | |||||||
| chr4:78601444 | T | C | 25 | a0001c0001t0001g0057 a0001c0001t0001g0266 a0001c0001t0001g0276 others(22): Show |
28 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.731-66T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601444 | |||||||
| chr4:78601454 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.731-56T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601454 | |||||||
| chr4:78601491 | T | C | 7 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(4): Show |
8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-19T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 10/12 | chr4 | 78601491 | |||||||
| chr4:78601844 | C | G | 3 | a0001c0001t0004g0265 a0002c0003t0004g0060 a0002c0003t0004g0061 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.789+276C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78601844 | |||||||
| chr4:78601864 | A | T | 1 | a0001c0001t0005g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.789+296A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78601864 | |||||||
| chr4:78601995 | C | T | 7 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(4): Show |
8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+427C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78601995 | |||||||
| chr4:78602013 | C | T | 1 | a0001c0001t0004g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.789+445C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602013 | |||||||
| chr4:78602097 | G | A | 1 | a0002c0003t0006g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.789+529G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602097 | |||||||
| chr4:78602175 | G | A | 3 | a0001c0002t0004g0148 a0005c0005t0003g0063 a0005c0005t0003g0080 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.789+607G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602175 | |||||||
| chr4:78602239 | C | CA | 24 | a0001c0001t0001g0057 a0001c0001t0001g0144 a0001c0001t0001g0225 others(21): Show |
27 | HG00323.hp2 HG00735.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.789+690dupA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 78602239 | ||||||
| chr4:78602239 | C | CAA | 10 | a0001c0001t0001g0266 a0001c0001t0001g0276 a0001c0001t0001g0285 others(7): Show |
10 | HG02280.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+689_789+690dup others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 78602239 | ||||||
| chr4:78602239 | CA | C | 13 | a0001c0001t0001g0104 a0001c0001t0001g0113 a0001c0001t0001g0173 others(10): Show |
13 | HG00558.hp1 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.789+690delA | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 78602239 | ||||||
| chr4:78602442 | A | G | 6 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(3): Show |
7 | HG02258.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.789+874A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602442 | |||||||
| chr4:78602541 | G | T | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+973G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602541 | |||||||
| chr4:78602543 | T | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+975T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602543 | |||||||
| chr4:78602544 | G | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+976G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602544 | |||||||
| chr4:78602547 | T | G | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+979T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602547 | |||||||
| chr4:78602548 | T | A | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+980T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602548 | |||||||
| chr4:78602562 | G | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+994G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602562 | |||||||
| chr4:78602563 | A | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+995A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602563 | |||||||
| chr4:78602568 | G | A | 22 | a0001c0001t0001g0057 a0001c0001t0001g0172 a0001c0001t0001g0209 others(19): Show |
25 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.789+1000G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602568 | |||||||
| chr4:78602589 | T | G | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1021T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602589 | |||||||
| chr4:78602590 | G | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1022G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602590 | |||||||
| chr4:78602592 | CTTTACTG others(29): Show |
C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1025_789+1060d others(38): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602592 | |||||||
| chr4:78602602 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.789+1034A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602602 | |||||||
| chr4:78602630 | C | T | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1062C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602630 | |||||||
| chr4:78602634 | T | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1066T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602634 | |||||||
| chr4:78602635 | T | G | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1067T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602635 | |||||||
| chr4:78602636 | A | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1068A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602636 | |||||||
| chr4:78602642 | A | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1074A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602642 | |||||||
| chr4:78602643 | G | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1075G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602643 | |||||||
| chr4:78602645 | C | G | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1077C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602645 | |||||||
| chr4:78602646 | C | A | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1078C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602646 | |||||||
| chr4:78602655 | T | A | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1087T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602655 | |||||||
| chr4:78602669 | T | C | 1 | a0001c0001t0003g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.789+1101T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602669 | |||||||
| chr4:78602768 | C | A | 4 | a0001c0001t0004g0265 a0002c0003t0004g0060 a0002c0003t0004g0061 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+1200C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602768 | |||||||
| chr4:78602828 | T | C | 7 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(4): Show |
8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+1260T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78602828 | |||||||
| chr4:78603023 | C | T | 2 | a0001c0001t0005g0036 a0001c0001t0005g0058 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.790-1254C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603023 | |||||||
| chr4:78603030 | T | G | 1 | a0001c0002t0004g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.790-1247T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603030 | |||||||
| chr4:78603035 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.790-1242G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603035 | |||||||
| chr4:78603037 | G | T | 1 | a0003c0004t0002g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.790-1240G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603037 | |||||||
| chr4:78603104 | C | G | 1 | a0001c0001t0001g0238 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.790-1173C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603104 | |||||||
| chr4:78603203 | A | G | 1 | a0001c0001t0003g0168 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.790-1074A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603203 | |||||||
| chr4:78603230 | G | T | 35 | a0001c0001t0001g0057 a0001c0001t0001g0266 a0001c0001t0001g0276 others(32): Show |
39 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.790-1047G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603230 | |||||||
| chr4:78603266 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.790-1011C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603266 | |||||||
| chr4:78603377 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.790-900A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603377 | |||||||
| chr4:78603548 | A | G | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.790-729A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603548 | |||||||
| chr4:78603631 | G | A | 1 | a0001c0001t0003g0221 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.790-646G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603631 | |||||||
| chr4:78603744 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.790-533C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603744 | |||||||
| chr4:78603868 | C | G | 16 | a0001c0001t0001g0057 a0001c0001t0002g0039 a0001c0001t0003g0017 others(13): Show |
19 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.790-409C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603868 | |||||||
| chr4:78603959 | T | G | 3 | a0001c0001t0006g0068 a0002c0003t0006g0011 a0002c0003t0006g0135 |
4 | HG02258.hp1 HG03041.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-318T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603959 | |||||||
| chr4:78603991 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.790-286C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78603991 | |||||||
| chr4:78604083 | A | G | 6 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(3): Show |
7 | HG02258.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-194A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78604083 | |||||||
| chr4:78604095 | T | C | 1 | a0001c0002t0004g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.790-182T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78604095 | |||||||
| chr4:78604250 | G | A | 71 | a0001c0001t0001g0158 a0001c0001t0002g0141 a0001c0001t0002g0199 others(68): Show |
81 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.790-27G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 11/12 | chr4 | 78604250 | |||||||
| chr4:78604430 | A | ATTTT | 15 | a0001c0001t0002g0039 a0001c0001t0003g0017 a0001c0001t0003g0048 others(12): Show |
18 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.912+32_912+35dupTT others(2): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78604430 | ||||||
| chr4:78604431 | T | C | 1 | a0001c0002t0004g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.912+32T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604431 | |||||||
| chr4:78604436 | CCCT | C | 15 | a0001c0001t0002g0039 a0001c0001t0003g0017 a0001c0001t0003g0048 others(12): Show |
18 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.912+38_912+40delCC others(1): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604436 | |||||||
| chr4:78604514 | A | G | 9 | a0001c0001t0001g0266 a0001c0001t0001g0276 a0001c0001t0001g0285 others(6): Show |
9 | HG02280.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.912+115A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604514 | |||||||
| chr4:78604562 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(104): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.912+163C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604562 | |||||||
| chr4:78604656 | T | C | 6 | a0001c0001t0006g0068 a0001c0002t0006g0277 a0002c0003t0006g0011 others(3): Show |
7 | HG02258.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.912+257T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604656 | |||||||
| chr4:78604705 | C | T | 1 | a0001c0002t0004g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.912+306C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604705 | |||||||
| chr4:78604824 | T | C | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.912+425T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604824 | |||||||
| chr4:78604844 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.912+445G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604844 | |||||||
| chr4:78604892 | G | A | 71 | a0001c0001t0001g0158 a0001c0001t0002g0141 a0001c0001t0002g0199 others(68): Show |
81 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.912+493G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604892 | |||||||
| chr4:78604955 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.912+556G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78604955 | |||||||
| chr4:78605149 | T | C | 9 | a0001c0001t0001g0266 a0001c0001t0001g0276 a0001c0001t0001g0285 others(6): Show |
9 | HG02280.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.912+750T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605149 | |||||||
| chr4:78605258 | C | T | 1 | a0001c0001t0003g0269 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.912+859C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605258 | |||||||
| chr4:78605278 | AG | A | 64 | a0001c0001t0001g0158 a0001c0001t0002g0141 a0001c0001t0002g0199 others(61): Show |
73 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.912+881delG | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78605278 | ||||||
| chr4:78605345 | A | G | 15 | a0001c0001t0002g0039 a0001c0001t0003g0017 a0001c0001t0003g0048 others(12): Show |
18 | HG00735.hp1 HG01884.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.912+946A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605345 | |||||||
| chr4:78605363 | A | G | 72 | a0001c0001t0001g0158 a0001c0001t0002g0141 a0001c0001t0002g0199 others(69): Show |
82 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.912+964A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605363 | |||||||
| chr4:78605484 | G | C | 85 | a0001c0001t0001g0158 a0001c0001t0001g0266 a0001c0001t0001g0276 others(82): Show |
95 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.912+1085G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605484 | |||||||
| chr4:78605787 | A | T | 14 | a0001c0001t0001g0266 a0001c0001t0001g0276 a0001c0001t0001g0285 others(11): Show |
14 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.912+1388A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605787 | |||||||
| chr4:78605814 | C | G | 104 | a0001c0001t0001g0158 a0001c0001t0001g0266 a0001c0001t0001g0276 others(101): Show |
117 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.912+1415C>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605814 | |||||||
| chr4:78605855 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(217): Show |
251 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.912+1456G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605855 | |||||||
| chr4:78605930 | G | A | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.912+1531G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78605930 | |||||||
| chr4:78606118 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
241 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.912+1719C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606118 | |||||||
| chr4:78606236 | G | T | 4 | a0001c0001t0004g0265 a0002c0003t0004g0060 a0002c0003t0004g0061 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+1837G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606236 | |||||||
| chr4:78606390 | T | A | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.912+1991T>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606390 | |||||||
| chr4:78606529 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0124 |
3 | HG00733.hp2 HG00735.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.912+2130T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606529 | |||||||
| chr4:78606566 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0228 a0001c0001t0001g0231 others(1): Show |
4 | HG00642.hp2 HG01070.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+2167C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606566 | |||||||
| chr4:78606675 | T | TTGAA | 2 | a0001c0001t0001g0024 a0001c0001t0001g0225 |
3 | HG01099.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.912+2297_912+2300d others(6): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78606675 | ||||||
| chr4:78606722 | A | T | 3 | a0001c0001t0006g0068 a0002c0003t0006g0011 a0002c0003t0006g0135 |
4 | HG02258.hp1 HG03041.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+2323A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606722 | |||||||
| chr4:78606794 | AT | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(180): Show |
212 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.912+2396delT | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606794 | |||||||
| chr4:78606872 | C | A | 4 | a0001c0001t0006g0068 a0001c0002t0006g0147 a0002c0003t0006g0011 others(1): Show |
5 | HG01891.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.912+2473C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78606872 | |||||||
| chr4:78607188 | A | G | 27 | a0001c0001t0004g0035 a0001c0001t0004g0055 a0001c0001t0004g0070 others(24): Show |
28 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.912+2789A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607188 | |||||||
| chr4:78607388 | AC | A | 6 | a0001c0001t0002g0022 a0001c0001t0002g0045 a0001c0001t0002g0161 others(3): Show |
7 | HG00280.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.913-2666delC | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78607388 | ||||||
| chr4:78607462 | AAG | A | 7 | a0001c0001t0006g0068 a0001c0002t0006g0147 a0001c0002t0006g0277 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-2592_913-2591d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78607462 | ||||||
| chr4:78607517 | A | T | 65 | a0001c0001t0002g0141 a0001c0001t0003g0005 a0001c0001t0003g0007 others(62): Show |
77 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.913-2539A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607517 | |||||||
| chr4:78607644 | CAT | C | 3 | a0001c0002t0006g0277 a0003c0004t0006g0081 a0003c0004t0006g0083 |
3 | HG02280.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.913-2410_913-2409d others(4): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 78607644 | ||||||
| chr4:78607659 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(114): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.913-2397G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607659 | |||||||
| chr4:78607687 | A | G | 2 | a0005c0005t0003g0063 a0005c0005t0003g0080 |
2 | HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.913-2369A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607687 | |||||||
| chr4:78607735 | T | C | 4 | a0001c0001t0006g0068 a0001c0002t0006g0147 a0002c0003t0006g0011 others(1): Show |
5 | HG01891.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.913-2321T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607735 | |||||||
| chr4:78607779 | G | T | 1 | a0001c0001t0003g0256 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.913-2277G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607779 | |||||||
| chr4:78607803 | G | T | 65 | a0001c0001t0002g0141 a0001c0001t0003g0005 a0001c0001t0003g0007 others(62): Show |
77 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.913-2253G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607803 | |||||||
| chr4:78607817 | C | T | 2 | a0001c0001t0004g0070 a0001c0001t0004g0071 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.913-2239C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607817 | |||||||
| chr4:78607982 | T | C | 1 | a0001c0001t0005g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.913-2074T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78607982 | |||||||
| chr4:78608051 | C | A | 1 | a0001c0001t0002g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.913-2005C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608051 | |||||||
| chr4:78608052 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(114): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.913-2004G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608052 | |||||||
| chr4:78608136 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.913-1920G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608136 | |||||||
| chr4:78608260 | G | A | 7 | a0001c0001t0006g0068 a0001c0002t0006g0147 a0001c0002t0006g0277 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-1796G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608260 | |||||||
| chr4:78608476 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(113): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.913-1580C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608476 | |||||||
| chr4:78608609 | G | C | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.913-1447G>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608609 | |||||||
| chr4:78608687 | G | A | 7 | a0001c0001t0004g0265 a0001c0002t0003g0050 a0002c0003t0004g0060 others(4): Show |
7 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.913-1369G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608687 | |||||||
| chr4:78608736 | G | A | 7 | a0001c0001t0006g0068 a0001c0002t0006g0147 a0001c0002t0006g0277 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-1320G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608736 | |||||||
| chr4:78608746 | C | A | 1 | a0001c0001t0002g0287 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.913-1310C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608746 | |||||||
| chr4:78608757 | G | A | 7 | a0001c0001t0006g0068 a0001c0002t0006g0147 a0001c0002t0006g0277 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-1299G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608757 | |||||||
| chr4:78608850 | A | T | 1 | a0004c0010t0004g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.913-1206A>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608850 | |||||||
| chr4:78608907 | C | T | 1 | a0001c0001t0006g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.913-1149C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608907 | |||||||
| chr4:78608998 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.913-1058T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78608998 | |||||||
| chr4:78609028 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.913-1028A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609028 | |||||||
| chr4:78609051 | C | T | 10 | a0001c0001t0004g0035 a0001c0001t0004g0055 a0001c0001t0004g0070 others(7): Show |
10 | HG02572.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.913-1005C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609051 | |||||||
| chr4:78609126 | G | T | 80 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0017 others(77): Show |
93 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.913-930G>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609126 | |||||||
| chr4:78609367 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.913-689C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609367 | |||||||
| chr4:78609431 | A | G | 2 | a0001c0002t0001g0077 a0001c0002t0001g0079 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.913-625A>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609431 | |||||||
| chr4:78609434 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.913-622C>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609434 | |||||||
| chr4:78609437 | T | G | 1 | a0001c0002t0004g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.913-619T>G | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609437 | |||||||
| chr4:78609578 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(135): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.913-478C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609578 | |||||||
| chr4:78609581 | G | A | 1 | a0001c0001t0004g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.913-475G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609581 | |||||||
| chr4:78609706 | C | T | 3 | a0001c0002t0006g0277 a0003c0004t0006g0081 a0003c0004t0006g0083 |
3 | HG02280.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.913-350C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609706 | |||||||
| chr4:78609884 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(123): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.913-172G>A | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609884 | |||||||
| chr4:78609904 | A | C | 66 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0017 others(63): Show |
78 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.913-152A>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609904 | |||||||
| chr4:78609924 | T | C | 4 | a0001c0001t0004g0265 a0002c0003t0004g0060 a0002c0003t0004g0061 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.913-132T>C | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78609924 | |||||||
| chr4:78610032 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(123): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.913-24C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78610032 | |||||||
| chr4:78610048 | C | T | 69 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0017 others(66): Show |
81 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
splice_region_variant&intron_variant | LOW | c.913-8C>T | ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 12/12 | chr4 | 78610048 |