Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 440073 |
|---|---|
| ensemblid | ENSG00000120645.12 |
| hgncid | 29193 |
| symbol | IQSEC3 |
| name | IQ motif and Sec7 domain ArfGEF 3 |
| refseq_nuc | NM_001170738.2 |
| refseq_prot | NP_001164209.1 |
| ensembl_nuc | ENST00000538872.6 |
| ensembl_prot | ENSP00000437554.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 66767 |
| end | 178455 |
| strand | + |
| ver | v1.2 |
| region | chr12:66767-178455 |
| region5000 | chr12:61767-183455 |
| regionname0 | IQSEC3_chr12_66767_178455 |
| regionname5000 | IQSEC3_chr12_61767_183455 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1182 | 125 | 21 | 23 | 59 | 7 | 14 | 34 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002 | 0/0 | 1182 | 69 | 29 | 11 | 16 | 3 | 10 | 9 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003 | 0/0 | 1182 | 27 | 18 | 6 | 2 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004 | 0/0 | 1182 | 13 | 3 | 1 | 8 | 0 | 1 | 7 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005 | 0/0 | 1182 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0006 | 1/0 | 1182 | 6 | 5 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007 | 0/0 | 1182 | 5 | 0 | 2 | 0 | 1 | 2 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0008 | 0/0 | 951 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0009 | 0/0 | 1182 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0010 | 0/0 | 1183 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0011 | 0/0 | 1182 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0012 | 0/0 | 1182 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0013 | 0/0 | 1182 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0014 | 0/0 | 1182 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0015 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0016 | 0/0 | 951 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0017 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0018 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0019 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0020 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0021 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0022 | 0/0 | 951 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0023 | 0/0 | 951 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0024 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0025 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0026 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3549 | 58 | 25 | 6 | 15 | 3 | 9 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0002 | 0/0 | 3549 | 35 | 3 | 6 | 18 | 2 | 6 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0003 | 0/0 | 3549 | 31 | 7 | 9 | 13 | 1 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0004 | 0/0 | 3549 | 21 | 6 | 2 | 7 | 2 | 4 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0005 | 0/0 | 3549 | 15 | 11 | 3 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0006 | 0/1 | 3549 | 14 | 0 | 2 | 8 | 2 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0007 | 0/0 | 3549 | 12 | 1 | 0 | 11 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0008 | 0/0 | 3549 | 7 | 1 | 1 | 5 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0009 | 0/0 | 3549 | 7 | 0 | 5 | 1 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0010 | 0/0 | 3549 | 7 | 5 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0011 | 0/0 | 3549 | 6 | 2 | 0 | 3 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0012 | 0/0 | 3549 | 5 | 5 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0013 | 0/0 | 3549 | 4 | 4 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0014 | 0/0 | 3552 | 3 | 0 | 0 | 3 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0015 | 0/0 | 3549 | 3 | 3 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0016 | 0/0 | 3569 | 3 | 3 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0017 | 0/0 | 3549 | 3 | 2 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0018 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0019 | 0/0 | 3549 | 2 | 0 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0020 | 0/0 | 3549 | 2 | 0 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0021 | 0/0 | 3549 | 2 | 0 | 1 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0022 | 0/0 | 3549 | 2 | 0 | 1 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0023 | 0/0 | 3549 | 2 | 0 | 1 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0024 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0025 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0026 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0027 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0028 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0029 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0030 | 1/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0031 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0032 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0033 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0034 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0035 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0036 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0037 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0038 | 0/0 | 3569 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0039 | 0/0 | 3569 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0040 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0041 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0042 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0043 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0044 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0045 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0046 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0047 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0048 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0049 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0050 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0051 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0052 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0053 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0054 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0055 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0056 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0057 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0058 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| c0059 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3539 | 69 | 15 | 19 | 23 | 3 | 8 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0002 | 0/1 | 3430 | 66 | 5 | 16 | 35 | 3 | 6 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0003 | 0/0 | 3535 | 18 | 0 | 1 | 10 | 2 | 5 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0004 | 0/0 | 3483 | 10 | 6 | 3 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0005 | 0/0 | 3532 | 8 | 8 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0006 | 0/0 | 3535 | 7 | 0 | 0 | 7 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0007 | 0/0 | 3539 | 7 | 5 | 1 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0008 | 0/0 | 3539 | 7 | 5 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0009 | 0/0 | 3483 | 7 | 7 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0010 | 0/0 | 3539 | 5 | 0 | 1 | 0 | 3 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0011 | 0/0 | 3528 | 5 | 0 | 0 | 1 | 0 | 4 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0012 | 0/0 | 3448 | 5 | 5 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0013 | 0/0 | 3539 | 4 | 4 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0014 | 0/0 | 3430 | 3 | 0 | 2 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0015 | 0/0 | 3578 | 3 | 2 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0016 | 0/0 | 3539 | 3 | 0 | 2 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0017 | 0/0 | 3535 | 2 | 0 | 0 | 2 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0018 | 0/0 | 3539 | 2 | 0 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0019 | 0/0 | 3535 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0020 | 0/0 | 3585 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0021 | 0/0 | 3535 | 2 | 0 | 0 | 2 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0022 | 0/0 | 3533 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0023 | 0/0 | 3482 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0024 | 0/0 | 3483 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0025 | 0/0 | 3483 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0026 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0027 | 0/0 | 3483 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0028 | 0/0 | 3489 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0029 | 0/0 | 3535 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0030 | 0/0 | 3539 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0031 | 0/0 | 3585 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0032 | 0/0 | 3539 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0033 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0034 | 0/0 | 3489 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0035 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0036 | 0/0 | 3535 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0037 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0038 | 0/0 | 3535 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0039 | 0/0 | 3537 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0040 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0041 | 0/0 | 3428 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0042 | 0/0 | 3533 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0043 | 0/0 | 3430 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0044 | 0/0 | 3430 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0045 | 0/0 | 3432 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0046 | 0/0 | 3539 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0047 | 0/0 | 3537 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0048 | 0/0 | 3535 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0049 | 0/0 | 3537 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0050 | 0/0 | 3533 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0051 | 0/0 | 3533 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0052 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0053 | 0/0 | 3430 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0054 | 0/0 | 3432 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0055 | 0/0 | 3380 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0056 | 0/0 | 3532 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0057 | 0/0 | 3532 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0058 | 0/0 | 3535 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0059 | 0/0 | 3535 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0060 | 0/0 | 3483 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0061 | 0/0 | 3539 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| t0062 | 0/0 | 3483 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 3549 | 35 | 3 | 6 | 18 | 2 | 6 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003 | 0/0 | 3549 | 31 | 7 | 9 | 13 | 1 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004 | 0/0 | 3549 | 21 | 6 | 2 | 7 | 2 | 4 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0006 | 0/1 | 3549 | 14 | 0 | 2 | 8 | 2 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0007 | 0/0 | 3549 | 12 | 1 | 0 | 11 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0019 | 0/0 | 3549 | 2 | 0 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0024 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0025 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0033 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0034 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0037 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0041 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0042 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0043 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0044 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0059 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001 | 0/0 | 3549 | 58 | 25 | 6 | 15 | 3 | 9 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0009 | 0/0 | 3549 | 7 | 0 | 5 | 1 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0015 | 0/0 | 3549 | 3 | 3 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0040 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005 | 0/0 | 3549 | 15 | 11 | 3 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0010 | 0/0 | 3549 | 7 | 5 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0017 | 0/0 | 3549 | 3 | 2 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0045 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0046 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0008 | 0/0 | 3549 | 7 | 1 | 1 | 5 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0011 | 0/0 | 3549 | 6 | 2 | 0 | 3 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0013 | 0/0 | 3549 | 4 | 4 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0018 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0031 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0006c0012 | 0/0 | 3549 | 5 | 5 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0006c0030 | 1/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0021 | 0/0 | 3549 | 2 | 0 | 1 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0048 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0049 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0050 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0008c0016 | 0/0 | 3569 | 3 | 3 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0008c0035 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0009c0020 | 0/0 | 3549 | 2 | 0 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0009c0051 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0010c0014 | 0/0 | 3552 | 3 | 0 | 0 | 3 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0011c0055 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0011c0058 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0012c0023 | 0/0 | 3549 | 2 | 0 | 1 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0013c0022 | 0/0 | 3549 | 2 | 0 | 1 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0014c0028 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0014c0029 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0015c0056 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0016c0057 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0017c0053 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0018c0054 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0019c0052 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0020c0047 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0021c0032 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0022c0038 | 0/0 | 3569 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0023c0039 | 0/0 | 3569 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0024c0036 | 0/0 | 3549 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0025c0027 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0026c0026 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 6978 | 29 | 3 | 6 | 14 | 2 | 4 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0002t0003 | 0/0 | 7083 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0002t0043 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0002t0044 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0002t0047 | 0/0 | 7085 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0002t0048 | 0/0 | 7083 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0002t0055 | 0/0 | 6928 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0001 | 0/0 | 7087 | 16 | 3 | 8 | 4 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0002 | 0/0 | 6978 | 5 | 0 | 0 | 5 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0004 | 0/0 | 7031 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0005 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0007 | 0/0 | 7087 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0010 | 0/0 | 7087 | 2 | 0 | 1 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0011 | 0/0 | 7076 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0012 | 0/0 | 6996 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0033 | 0/0 | 7087 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0003t0039 | 0/0 | 7085 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0001 | 0/0 | 7087 | 7 | 1 | 0 | 3 | 0 | 3 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0002 | 0/0 | 6978 | 2 | 1 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0003 | 0/0 | 7083 | 3 | 0 | 0 | 2 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0004 | 0/0 | 7031 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0011 | 0/0 | 7076 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0012 | 0/0 | 6996 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0016 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0035 | 0/0 | 7137 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0037 | 0/0 | 7087 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0058 | 0/0 | 7083 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0004t0060 | 0/0 | 7031 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0006t0002 | 0/1 | 6978 | 11 | 0 | 2 | 8 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0006t0010 | 0/0 | 7087 | 2 | 0 | 0 | 0 | 2 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0006t0049 | 0/0 | 7085 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0007t0001 | 0/0 | 7087 | 12 | 1 | 0 | 11 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0019t0001 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0019t0034 | 0/0 | 7037 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0024t0001 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0025t0040 | 0/0 | 7087 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0033t0013 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0034t0001 | 0/0 | 7087 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0037t0011 | 0/0 | 7076 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0041t0056 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0042t0001 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0043t0004 | 0/0 | 7031 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0044t0001 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0001c0059t0001 | 0/0 | 7087 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0001 | 0/0 | 7087 | 8 | 4 | 1 | 1 | 1 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0002 | 0/0 | 6978 | 6 | 0 | 0 | 4 | 1 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0003 | 0/0 | 7083 | 8 | 0 | 1 | 4 | 1 | 2 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0004 | 0/0 | 7031 | 3 | 2 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0005 | 0/0 | 7080 | 5 | 5 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0006 | 0/0 | 7083 | 4 | 0 | 0 | 4 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0008 | 0/0 | 7087 | 6 | 4 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0009 | 0/0 | 7031 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0011 | 0/0 | 7076 | 2 | 0 | 0 | 0 | 0 | 2 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0013 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0016 | 0/0 | 7087 | 2 | 0 | 1 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0020 | 0/0 | 7133 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0021 | 0/0 | 7083 | 2 | 0 | 0 | 2 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0022 | 0/0 | 7081 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0024 | 0/0 | 7031 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0036 | 0/0 | 7083 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0041 | 0/0 | 6976 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0050 | 0/0 | 7081 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0001t0051 | 0/0 | 7081 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0009t0002 | 0/0 | 6978 | 7 | 0 | 5 | 1 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0015t0013 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0015t0031 | 0/0 | 7133 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0015t0046 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0002c0040t0029 | 0/0 | 7083 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0002 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0003 | 0/0 | 7083 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0009 | 0/0 | 7031 | 4 | 4 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0012 | 0/0 | 6996 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0013 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0019 | 0/0 | 7083 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0023 | 0/0 | 7030 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0025 | 0/0 | 7031 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0028 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0059 | 0/0 | 7083 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0005t0062 | 0/0 | 7031 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0010t0002 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0010t0007 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0010t0012 | 0/0 | 6996 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0010t0015 | 0/0 | 7126 | 2 | 1 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0010t0019 | 0/0 | 7083 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0010t0020 | 0/0 | 7133 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0017t0002 | 0/0 | 6978 | 2 | 1 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0017t0015 | 0/0 | 7126 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0045t0045 | 0/0 | 6980 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0003c0046t0001 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0008t0001 | 0/0 | 7087 | 3 | 0 | 1 | 2 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0008t0002 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0008t0003 | 0/0 | 7083 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0008t0052 | 0/0 | 7028 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0008t0053 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0011t0003 | 0/0 | 7083 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0011t0004 | 0/0 | 7031 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0004c0011t0006 | 0/0 | 7083 | 3 | 0 | 0 | 3 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0013t0001 | 0/0 | 7087 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0013t0009 | 0/0 | 7031 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0013t0025 | 0/0 | 7031 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0018t0001 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0018t0008 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0005c0031t0001 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0006c0012t0001 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0006c0012t0004 | 0/0 | 7031 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0006c0012t0005 | 0/0 | 7080 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0006c0012t0032 | 0/0 | 7087 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0006c0030t0001 | 1/0 | 7087 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0021t0001 | 0/0 | 7087 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0021t0004 | 0/0 | 7031 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0048t0001 | 0/0 | 7087 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0049t0002 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0007c0050t0010 | 0/0 | 7087 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0008c0016t0007 | 0/0 | 7107 | 2 | 2 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0008c0016t0061 | 0/0 | 7107 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0008c0035t0007 | 0/0 | 7107 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0009c0020t0001 | 0/0 | 7087 | 2 | 0 | 2 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0009c0051t0001 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0010c0014t0001 | 0/0 | 7090 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0010c0014t0003 | 0/0 | 7086 | 2 | 0 | 0 | 2 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0011c0055t0018 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0011c0058t0027 | 0/0 | 7031 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0012c0023t0017 | 0/0 | 7083 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0012c0023t0018 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0013c0022t0001 | 0/0 | 7087 | 2 | 0 | 1 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0014c0028t0001 | 0/0 | 7087 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0014c0029t0054 | 0/0 | 6980 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0015c0056t0017 | 0/0 | 7083 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0016c0057t0014 | 0/0 | 6998 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0017c0053t0026 | 0/0 | 6983 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0018c0054t0014 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0019c0052t0014 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0020c0047t0042 | 0/0 | 7078 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0021c0032t0001 | 0/0 | 7087 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0022c0038t0007 | 0/0 | 7107 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0023c0039t0030 | 0/0 | 7107 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0024c0036t0057 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0025c0027t0038 | 0/0 | 7083 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| a0026c0026t0003 | 0/0 | 7083 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | copy fasta | chr12 | 61767 | 183455 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0043g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0044g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0047g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0048g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0002t0055g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0010g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0010g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0033g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0003t0039g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0011g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0016g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0035g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0037g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0058g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0004t0060g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0002g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0010g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0010g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0006t0049g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0007t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0019t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0019t0034g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0024t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0025t0040g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0033t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0034t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0037t0011g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0041t0056g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0042t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0043t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0044t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0001c0059t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0008g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0011g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0011g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0013g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0016g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0016g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0020g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0021g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0021g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0022g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0022g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0024g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0024g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0036g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0041g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0050g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0001t0051g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0009t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0009t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0009t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0009t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0009t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0009t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0009t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0015t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0015t0031g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0015t0046g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0002c0040t0029g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0019g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0023g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0023g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0025g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0028g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0059g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0005t0062g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0010t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0010t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0010t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0010t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0010t0015g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0010t0019g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0010t0020g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0017t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0017t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0017t0015g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0045t0045g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0003c0046t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0008t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0008t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0008t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0008t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0008t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0008t0052g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0008t0053g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0011t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0011t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0011t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0011t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0011t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0004c0011t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0005c0013t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0005c0013t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0005c0013t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0005c0013t0025g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0005c0018t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0005c0018t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0005c0031t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0006c0012t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0006c0012t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0006c0012t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0006c0012t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0006c0012t0032g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0006c0030t0001g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0007c0021t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0007c0021t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0007c0048t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0007c0049t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0007c0050t0010g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0008c0016t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0008c0016t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0008c0016t0061g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0008c0035t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0009c0020t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0009c0020t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0009c0051t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0010c0014t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0010c0014t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0010c0014t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0011c0055t0018g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0011c0058t0027g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0012c0023t0017g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0012c0023t0018g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0013c0022t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0013c0022t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0014c0028t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0014c0029t0054g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0015c0056t0017g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0016c0057t0014g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0017c0053t0026g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0018c0054t0014g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0019c0052t0014g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0020c0047t0042g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0021c0032t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0022c0038t0007g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0023c0039t0030g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0024c0036t0057g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0025c0027t0038g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| a0026c0026t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0182 | EUR | GBR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00099 | hp2 | a0013 | c0022 | t0001 | g0237 | EUR | GBR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00280 | hp1 | a0001 | c0003 | t0010 | g0155 | EUR | FIN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00280 | hp2 | a0023 | c0039 | t0030 | g0094 | EUR | FIN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0261 | EUR | FIN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00323 | hp2 | a0002 | c0001 | t0003 | g0216 | EUR | FIN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00408 | hp2 | a0003 | c0017 | t0002 | g0089 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00438 | hp1 | a0002 | c0009 | t0002 | g0213 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00438 | hp2 | a0002 | c0001 | t0006 | g0151 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00597 | hp1 | a0001 | c0007 | t0001 | g0083 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00597 | hp2 | a0003 | c0045 | t0045 | g0160 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00621 | hp1 | a0002 | c0001 | t0021 | g0163 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00621 | hp2 | a0001 | c0006 | t0002 | g0106 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00642 | hp1 | a0002 | c0001 | t0003 | g0183 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00642 | hp2 | a0001 | c0006 | t0002 | g0145 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00673 | hp1 | a0010 | c0014 | t0003 | g0002 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00673 | hp2 | a0001 | c0025 | t0040 | g0148 | EAS | CHS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00733 | hp1 | a0007 | c0021 | t0004 | g0253 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00733 | hp2 | a0016 | c0057 | t0014 | g0274 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00735 | hp1 | a0003 | c0005 | t0059 | g0061 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00735 | hp2 | a0002 | c0009 | t0002 | g0222 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00741 | hp1 | a0009 | c0051 | t0001 | g0242 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0098 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01070 | hp1 | a0009 | c0020 | t0001 | g0211 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01070 | hp2 | a0001 | c0019 | t0001 | g0139 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01074 | hp1 | a0002 | c0001 | t0008 | g0020 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01074 | hp2 | a0001 | c0003 | t0010 | g0232 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01081 | hp1 | a0013 | c0022 | t0001 | g0259 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01081 | hp2 | a0014 | c0029 | t0054 | g0059 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01106 | hp1 | a0003 | c0010 | t0015 | g0266 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0184 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01167 | hp1 | a0014 | c0028 | t0001 | g0062 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01167 | hp2 | a0003 | c0005 | t0002 | g0252 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01168 | hp1 | a0001 | c0019 | t0034 | g0244 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01168 | hp2 | a0001 | c0006 | t0002 | g0188 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01175 | hp2 | a0011 | c0055 | t0018 | g0271 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01243 | hp1 | a0002 | c0001 | t0004 | g0028 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01243 | hp2 | a0002 | c0001 | t0016 | g0241 | AMR | PUR | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01255 | hp1 | a0002 | c0009 | t0002 | g0270 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01255 | hp2 | a0001 | c0042 | t0001 | g0243 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0204 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01258 | hp1 | a0001 | c0004 | t0016 | g0223 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0127 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0126 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01346 | hp2 | a0003 | c0046 | t0001 | g0229 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01358 | hp1 | a0002 | c0001 | t0008 | g0026 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01358 | hp2 | a0008 | c0035 | t0007 | g0135 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01361 | hp1 | a0003 | c0010 | t0002 | g0203 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01361 | hp2 | a0012 | c0023 | t0018 | g0276 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01496 | hp1 | a0001 | c0004 | t0004 | g0031 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01516 | hp1 | a0001 | c0006 | t0010 | g0209 | EUR | IBS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01516 | hp2 | a0001 | c0004 | t0035 | g0030 | EUR | IBS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01517 | hp1 | a0001 | c0004 | t0003 | g0082 | EUR | IBS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01517 | hp2 | a0001 | c0006 | t0010 | g0210 | EUR | IBS | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01884 | hp2 | a0003 | c0010 | t0020 | g0078 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01891 | hp1 | a0002 | c0001 | t0009 | g0192 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01891 | hp2 | a0006 | c0012 | t0032 | g0264 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0111 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01943 | hp1 | a0002 | c0009 | t0002 | g0249 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0113 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01952 | hp1 | a0003 | c0005 | t0062 | g0073 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01975 | hp1 | a0018 | c0054 | t0014 | g0279 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0157 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01981 | hp1 | a0002 | c0009 | t0002 | g0262 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01981 | hp2 | a0004 | c0008 | t0001 | g0129 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0045 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01993 | hp2 | a0009 | c0020 | t0001 | g0238 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02015 | hp2 | a0001 | c0007 | t0001 | g0118 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02027 | hp1 | a0001 | c0002 | t0044 | g0084 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0109 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02055 | hp1 | a0002 | c0001 | t0005 | g0054 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02055 | hp2 | a0001 | c0003 | t0012 | g0049 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02056 | hp1 | a0001 | c0003 | t0039 | g0116 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02056 | hp2 | a0019 | c0052 | t0014 | g0278 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02071 | hp1 | a0001 | c0006 | t0002 | g0189 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02071 | hp2 | a0002 | c0001 | t0003 | g0190 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02074 | hp2 | a0010 | c0014 | t0003 | g0043 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02080 | hp1 | a0004 | c0008 | t0001 | g0212 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02080 | hp2 | a0001 | c0007 | t0001 | g0150 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02129 | hp2 | a0001 | c0006 | t0002 | g0154 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02135 | hp1 | a0001 | c0007 | t0001 | g0152 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02135 | hp2 | a0002 | c0001 | t0003 | g0041 | EAS | KHV | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02145 | hp1 | a0001 | c0003 | t0007 | g0003 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02145 | hp2 | a0002 | c0040 | t0029 | g0156 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | CDX | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0102 | EAS | CDX | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02165 | hp2 | a0001 | c0002 | t0048 | g0105 | EAS | CDX | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0202 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02257 | hp2 | a0003 | c0005 | t0025 | g0024 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0172 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02273 | hp2 | a0002 | c0009 | t0002 | g0080 | AMR | PEL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02280 | hp1 | a0005 | c0031 | t0001 | g0057 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02280 | hp2 | a0008 | c0016 | t0061 | g0015 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02451 | hp1 | a0005 | c0013 | t0025 | g0115 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02451 | hp2 | a0002 | c0001 | t0051 | g0013 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02572 | hp1 | a0002 | c0001 | t0022 | g0038 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02572 | hp2 | a0005 | c0013 | t0001 | g0251 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02615 | hp1 | a0004 | c0011 | t0004 | g0159 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02615 | hp2 | a0003 | c0005 | t0023 | g0245 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02622 | hp1 | a0001 | c0033 | t0013 | g0147 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02622 | hp2 | a0008 | c0016 | t0007 | g0037 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02630 | hp1 | a0001 | c0004 | t0058 | g0185 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02630 | hp2 | a0002 | c0001 | t0024 | g0177 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02647 | hp1 | a0002 | c0001 | t0005 | g0005 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02647 | hp2 | a0001 | c0004 | t0060 | g0217 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02683 | hp1 | a0021 | c0032 | t0001 | g0108 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02683 | hp2 | a0002 | c0001 | t0003 | g0215 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02698 | hp1 | a0001 | c0002 | t0047 | g0201 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0133 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02717 | hp1 | a0002 | c0001 | t0005 | g0007 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0103 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0195 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02738 | hp2 | a0007 | c0048 | t0001 | g0221 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02809 | hp1 | a0002 | c0001 | t0005 | g0012 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02809 | hp2 | a0002 | c0001 | t0001 | g0019 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02818 | hp1 | a0002 | c0001 | t0008 | g0025 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02818 | hp2 | a0002 | c0015 | t0046 | g0224 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02886 | hp1 | a0006 | c0012 | t0001 | g0265 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02886 | hp2 | a0002 | c0001 | t0005 | g0014 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02896 | hp1 | a0001 | c0004 | t0012 | g0022 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02896 | hp2 | a0002 | c0015 | t0031 | g0207 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02897 | hp1 | a0001 | c0004 | t0012 | g0021 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02897 | hp2 | a0006 | c0012 | t0004 | g0065 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02922 | hp1 | a0002 | c0001 | t0004 | g0027 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02922 | hp2 | a0003 | c0005 | t0019 | g0226 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02965 | hp1 | a0002 | c0001 | t0008 | g0052 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02965 | hp2 | a0006 | c0012 | t0005 | g0016 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02970 | hp1 | a0001 | c0044 | t0001 | g0050 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02970 | hp2 | a0001 | c0003 | t0005 | g0193 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02976 | hp1 | a0003 | c0005 | t0012 | g0074 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03017 | hp1 | a0001 | c0004 | t0001 | g0180 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03017 | hp2 | a0001 | c0037 | t0011 | g0194 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03041 | hp1 | a0005 | c0013 | t0001 | g0250 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03041 | hp2 | a0003 | c0010 | t0007 | g0268 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03098 | hp1 | a0002 | c0001 | t0013 | g0011 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03098 | hp2 | a0003 | c0005 | t0023 | g0068 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03139 | hp1 | a0002 | c0001 | t0050 | g0051 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03139 | hp2 | a0024 | c0036 | t0057 | g0048 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03209 | hp1 | a0002 | c0001 | t0001 | g0191 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03209 | hp2 | a0001 | c0041 | t0056 | g0072 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03225 | hp1 | a0005 | c0018 | t0001 | g0248 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0091 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03239 | hp1 | a0001 | c0002 | t0055 | g0256 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03239 | hp2 | a0001 | c0006 | t0049 | g0144 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03453 | hp1 | a0002 | c0001 | t0022 | g0087 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03453 | hp2 | a0002 | c0001 | t0020 | g0071 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03486 | hp1 | a0003 | c0017 | t0002 | g0069 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03486 | hp2 | a0003 | c0010 | t0012 | g0034 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03516 | hp1 | a0002 | c0001 | t0004 | g0029 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03516 | hp2 | a0002 | c0001 | t0024 | g0017 | AFR | ESN | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03540 | hp1 | a0003 | c0010 | t0019 | g0178 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03540 | hp2 | a0005 | c0013 | t0009 | g0246 | AFR | GWD | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03579 | hp1 | a0003 | c0005 | t0009 | g0009 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03579 | hp2 | a0003 | c0017 | t0015 | g0056 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0090 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03654 | hp2 | a0002 | c0001 | t0036 | g0161 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03669 | hp1 | a0002 | c0001 | t0003 | g0181 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03669 | hp2 | a0001 | c0004 | t0001 | g0170 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0167 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03688 | hp2 | a0002 | c0001 | t0041 | g0168 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03704 | hp1 | a0002 | c0001 | t0002 | g0047 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03704 | hp2 | a0026 | c0026 | t0003 | g0165 | SAS | PJL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03831 | hp1 | a0002 | c0001 | t0011 | g0124 | SAS | BEB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03831 | hp2 | a0001 | c0004 | t0001 | g0053 | SAS | BEB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG04115 | hp1 | a0001 | c0059 | t0001 | g0233 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG04115 | hp2 | a0002 | c0001 | t0011 | g0162 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0101 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG04199 | hp2 | a0004 | c0011 | t0003 | g0046 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG04204 | hp1 | a0001 | c0004 | t0011 | g0200 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG04204 | hp2 | a0002 | c0009 | t0002 | g0081 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG04228 | hp1 | a0003 | c0005 | t0003 | g0033 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG04228 | hp2 | a0002 | c0001 | t0016 | g0121 | SAS | STU | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18522 | hp1 | a0002 | c0001 | t0009 | g0064 | AFR | YRI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | YRI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18612 | hp1 | a0001 | c0006 | t0002 | g0136 | EAS | CHB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18612 | hp2 | a0002 | c0001 | t0003 | g0140 | EAS | CHB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18747 | hp1 | a0001 | c0007 | t0001 | g0075 | EAS | CHB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18747 | hp2 | a0001 | c0004 | t0037 | g0208 | EAS | CHB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18906 | hp1 | a0003 | c0005 | t0009 | g0055 | AFR | YRI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18906 | hp2 | a0006 | c0012 | t0005 | g0006 | AFR | YRI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18941 | hp1 | a0001 | c0003 | t0004 | g0166 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18941 | hp2 | a0001 | c0003 | t0002 | g0169 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18942 | hp1 | a0001 | c0004 | t0001 | g0235 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18942 | hp2 | a0011 | c0058 | t0027 | g0272 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18943 | hp1 | a0001 | c0003 | t0033 | g0110 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18943 | hp2 | a0015 | c0056 | t0017 | g0273 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18944 | hp1 | a0004 | c0008 | t0003 | g0079 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18944 | hp2 | a0002 | c0001 | t0006 | g0175 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18947 | hp1 | a0001 | c0007 | t0001 | g0107 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18947 | hp2 | a0001 | c0003 | t0002 | g0219 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18948 | hp1 | a0025 | c0027 | t0038 | g0040 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18950 | hp1 | a0002 | c0001 | t0021 | g0164 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18950 | hp2 | a0002 | c0001 | t0002 | g0120 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18957 | hp2 | a0001 | c0007 | t0001 | g0042 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18959 | hp2 | a0001 | c0007 | t0001 | g0117 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18962 | hp2 | a0001 | c0004 | t0002 | g0142 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18963 | hp2 | a0001 | c0003 | t0002 | g0060 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18973 | hp1 | a0004 | c0011 | t0006 | g0128 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18973 | hp2 | a0001 | c0002 | t0043 | g0131 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18975 | hp1 | a0001 | c0007 | t0001 | g0149 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18975 | hp2 | a0001 | c0006 | t0002 | g0196 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18983 | hp1 | a0004 | c0008 | t0001 | g0173 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18983 | hp2 | a0004 | c0011 | t0006 | g0093 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18985 | hp1 | a0002 | c0001 | t0002 | g0119 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18985 | hp2 | a0001 | c0007 | t0001 | g0122 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18986 | hp1 | a0001 | c0006 | t0002 | g0104 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18986 | hp2 | a0010 | c0014 | t0001 | g0076 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0277 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18994 | hp2 | a0002 | c0001 | t0002 | g0143 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18995 | hp1 | a0001 | c0034 | t0001 | g0214 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA18995 | hp2 | a0001 | c0006 | t0002 | g0095 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19004 | hp1 | a0001 | c0006 | t0002 | g0092 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19004 | hp2 | a0002 | c0001 | t0006 | g0097 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19007 | hp2 | a0002 | c0001 | t0006 | g0085 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19010 | hp1 | a0001 | c0004 | t0003 | g0198 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19011 | hp1 | a0004 | c0008 | t0002 | g0130 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19011 | hp2 | a0017 | c0053 | t0026 | g0275 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | LWK | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19030 | hp2 | a0008 | c0016 | t0007 | g0058 | AFR | LWK | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19043 | hp1 | a0003 | c0005 | t0028 | g0228 | AFR | LWK | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0070 | AFR | LWK | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19062 | hp1 | a0001 | c0004 | t0003 | g0197 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19063 | hp1 | a0004 | c0008 | t0053 | g0199 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19063 | hp2 | a0002 | c0001 | t0003 | g0234 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19077 | hp1 | a0001 | c0003 | t0011 | g0138 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19081 | hp1 | a0004 | c0011 | t0006 | g0132 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19089 | hp1 | a0012 | c0023 | t0017 | g0280 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19089 | hp2 | a0001 | c0007 | t0001 | g0153 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19090 | hp1 | a0002 | c0001 | t0002 | g0171 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0174 | EAS | JPT | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0225 | AFR | YRI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA19240 | hp2 | a0002 | c0001 | t0008 | g0023 | AFR | YRI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20129 | hp1 | a0004 | c0008 | t0052 | g0247 | AFR | ASW | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20129 | hp2 | a0003 | c0005 | t0013 | g0036 | AFR | ASW | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20752 | hp1 | a0007 | c0021 | t0001 | g0230 | EUR | TSI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0134 | EUR | TSI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20805 | hp1 | a0022 | c0038 | t0007 | g0255 | EUR | TSI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20805 | hp2 | a0002 | c0001 | t0002 | g0260 | EUR | TSI | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20905 | hp1 | a0007 | c0050 | t0010 | g0220 | SAS | GIH | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0137 | SAS | GIH | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01123 | hp1 | a0007 | c0049 | t0002 | g0231 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG01123 | hp2 | a0001 | c0024 | t0001 | g0032 | AMR | CLM | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02109 | hp1 | a0002 | c0015 | t0013 | g0018 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02486 | hp1 | a0003 | c0005 | t0009 | g0281 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG02486 | hp2 | a0005 | c0018 | t0008 | g0227 | AFR | ACB | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03471 | hp1 | a0003 | c0010 | t0015 | g0263 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG03471 | hp2 | a0001 | c0003 | t0007 | g0004 | AFR | MSL | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG06807 | hp1 | a0001 | c0043 | t0004 | g0063 | AFR | USA | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| HG06807 | hp2 | a0003 | c0005 | t0009 | g0077 | AFR | USA | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20300 | hp1 | a0002 | c0001 | t0008 | g0067 | AFR | USA | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0206 | AFR | USA | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA21309 | hp1 | a0004 | c0011 | t0004 | g0146 | AFR | LWK | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| NA21309 | hp2 | a0020 | c0047 | t0042 | g0236 | AFR | LWK | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0006 | t0002 | g0258 | REF | REF | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| homoSapiens_grch38 | hp1 | a0006 | c0030 | t0001 | g0269 | REF | REF | IQSEC3_chr12_61767_183455 | IQSEC3 | chr12 | 61767 | 183455 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:66923
|
A | G | 7 | a0011a0012a0015others(4): Show | 9 | HG00733.hp2 HG01175.hp2 HG01361.hp2 others(6): Show |
missense_variant | MODERATE | c.41A>G | p.Tyr14Cys | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/14 | 157/7087 | 41/3549 | 14/1182 | chr12 | 66923 | ||
| chr12:66954
|
C | G | 7 | a0011a0012a0015others(4): Show | 9 | HG00733.hp2 HG01175.hp2 HG01361.hp2 others(6): Show |
missense_variant | MODERATE | c.72C>G | p.Asn24Lys | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/14 | 188/7087 | 72/3549 | 24/1182 | chr12 | 66954 | ||
| chr12:66973
|
A | T | 4 | a0007a0009a0013others(1): Show | 11 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(8): Show |
missense_variant | MODERATE | c.91A>T | p.Thr31Ser | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/14 | 207/7087 | 91/3549 | 31/1182 | chr12 | 66973 | ||
| chr12:67024
|
G | A | 4 | a0012a0017a0018others(1): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
missense_variant | MODERATE | c.142G>A | p.Ala48Thr | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/14 | 258/7087 | 142/3549 | 48/1182 | chr12 | 67024 | ||
| chr12:67299
|
C | G | 4 | a0012a0017a0018others(1): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
missense_variant | MODERATE | c.417C>G | p.His139Gln | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/14 | 533/7087 | 417/3549 | 139/1182 | chr12 | 67299 | ||
| chr12:125796
|
G | A | 1 | a0026 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.787G>A | p.Gly263Ser | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/14 | 903/7087 | 787/3549 | 263/1182 | chr12 | 125796 | ||
| chr12:125820
|
G | A | 1 | a0025 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.811G>A | p.Gly271Ser | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/14 | 927/7087 | 811/3549 | 271/1182 | chr12 | 125820 | ||
| chr12:125856
|
C | T | 22 | a0001a0002a0003others(19): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
missense_variant | MODERATE | c.847C>T | p.Pro283Ser | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/14 | 963/7087 | 847/3549 | 283/1182 | chr12 | 125856 | ||
| chr12:138343
|
G | A | 1 | a0021 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.980G>A | p.Arg327His | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/14 | 1096/7087 | 980/3549 | 327/1182 | chr12 | 138343 | ||
| chr12:138757
|
A | G | 4 | a0003a0005a0013others(1): Show | 37 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(34): Show |
missense_variant | MODERATE | c.1394A>G | p.Asp465Gly | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/14 | 1510/7087 | 1394/3549 | 465/1182 | chr12 | 138757 | ||
| chr12:138905
|
G | C | 5 | a0004a0015a0017others(2): Show | 17 | HG01981.hp2 HG02080.hp1 HG02615.hp1 others(14): Show |
missense_variant | MODERATE | c.1542G>C | p.Gln514His | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/14 | 1658/7087 | 1542/3549 | 514/1182 | chr12 | 138905 | ||
| chr12:139036
|
C | G | 13 | a0001a0003a0005others(10): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
missense_variant | MODERATE | c.1673C>G | p.Ala558Gly | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/14 | 1789/7087 | 1673/3549 | 558/1182 | chr12 | 139036 | ||
| chr12:139085
|
A | AGAG | 1 | a0010 | 3 | HG00673.hp1 HG02074.hp2 NA18986.hp2 |
conservative_inframe_insertion | MODERATE | c.1735_1737dupGAG | p.Glu579dup | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/14 | 1854/7087 | 1738/3549 | 580/1182 | INFO_REALIGN_3_PRIME | chr12 | 139085 | |
| chr12:163586
|
G | C | 1 | a0018 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.2676G>C | p.Gln892His | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/14 | 2792/7087 | 2676/3549 | 892/1182 | chr12 | 163586 | ||
| chr12:174726
|
C | T | 1 | a0024 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.3242C>T | p.Pro1081Leu | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3358/7087 | 3242/3549 | 1081/1182 | chr12 | 174726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:66915
|
C | T | 1 | a0001c0059 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.33C>T | p.Ala11Ala | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/14 | 149/7087 | 33/3549 | 11/1182 | chr12 | 66915 | ||
| chr12:67053
|
G | A | 1 | a0001c0024 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.171G>A | p.Gln57Gln | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/14 | 287/7087 | 171/3549 | 57/1182 | chr12 | 67053 | ||
| chr12:125747
|
G | A | 1 | a0001c0025 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.738G>A | p.Leu246Leu | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/14 | 854/7087 | 738/3549 | 246/1182 | chr12 | 125747 | ||
| chr12:138470
|
G | A | 1 | a0007c0048 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1107G>A | p.Ala369Ala | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/14 | 1223/7087 | 1107/3549 | 369/1182 | chr12 | 138470 | ||
| chr12:138734
|
G | A | 15 | a0001c0004a0001c0006a0001c0007others(12): Show | 61 | HG00597.hp1 HG00621.hp2 HG00642.hp2 others(58): Show |
synonymous_variant | LOW | c.1371G>A | p.Glu457Glu | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/14 | 1487/7087 | 1371/3549 | 457/1182 | chr12 | 138734 | ||
| chr12:138989
|
C | T | 12 | a0001c0037a0001c0043a0001c0044others(9): Show | 39 | HG00099.hp2 HG00408.hp2 HG00735.hp1 others(36): Show |
synonymous_variant | LOW | c.1626C>T | p.Ala542Ala | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/14 | 1742/7087 | 1626/3549 | 542/1182 | chr12 | 138989 | ||
| chr12:141160
|
C | T | 1 | a0001c0042 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.2028C>T | p.Arg676Arg | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/14 | 2144/7087 | 2028/3549 | 676/1182 | chr12 | 141160 | ||
| chr12:157100
|
T | C | 8 | a0001c0033a0001c0041a0001c0043others(5): Show | 27 | HG00597.hp2 HG00735.hp1 HG01167.hp1 others(24): Show |
synonymous_variant | LOW | c.2229T>C | p.Arg743Arg | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 6/14 | 2345/7087 | 2229/3549 | 743/1182 | chr12 | 157100 | ||
| chr12:165481
|
T | C | 14 | a0001c0002a0001c0006a0001c0034others(11): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
synonymous_variant | LOW | c.2757T>C | p.Phe919Phe | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 10/14 | 2873/7087 | 2757/3549 | 919/1182 | chr12 | 165481 | ||
| chr12:174892
|
T | C | 49 | a0001c0002a0001c0003a0001c0004others(46): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
synonymous_variant | LOW | c.3408T>C | p.Gly1136Gly | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3524/7087 | 3408/3549 | 1136/1182 | chr12 | 174892 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:66802
|
G | C | 9 | a0011c0055t0018a0011c0058t0027a0012c0023t0017others(6): Show | 9 | HG00733.hp2 HG01175.hp2 HG01361.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-81G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/14 | 81 | chr12 | 66802 | |||||
| chr12:175124
|
C | T | 1 | a0003c0005t0062 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 91 | chr12 | 175124 | |||||
| chr12:175398
|
G | T | 9 | a0001c0004t0060a0002c0001t0009a0002c0001t0024others(6): Show | 14 | HG01891.hp1 HG01952.hp1 HG02257.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*365G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 365 | chr12 | 175398 | |||||
| chr12:175428
|
G | A | 4 | a0002c0001t0020a0003c0005t0019a0003c0010t0019others(1): Show | 4 | HG01884.hp2 HG02922.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*395G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 395 | chr12 | 175428 | |||||
| chr12:175519
|
C | A | 2 | a0003c0005t0019a0003c0010t0019 | 2 | HG02922.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*486C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 486 | chr12 | 175519 | |||||
| chr12:175527
|
G | A | 2 | a0003c0010t0015a0003c0017t0015 | 3 | HG01106.hp1 HG03471.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*494G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 494 | chr12 | 175527 | |||||
| chr12:175538
|
G | T | 5 | a0002c0001t0009a0003c0005t0009a0003c0005t0062others(2): Show | 9 | HG01891.hp1 HG01952.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*505G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 505 | chr12 | 175538 | |||||
| chr12:175589
|
T | C | 1 | a0003c0005t0028 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 556 | chr12 | 175589 | |||||
| chr12:175759
|
G | T | 4 | a0001c0004t0058a0002c0001t0008a0003c0005t0059others(1): Show | 9 | HG00735.hp1 HG01074.hp1 HG01358.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*726G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 726 | chr12 | 175759 | |||||
| chr12:175760
|
G | A | 1 | a0002c0001t0021 | 2 | HG00621.hp1 NA18950.hp1 |
3_prime_UTR_variant | MODIFIER | c.*727G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 727 | chr12 | 175760 | |||||
| chr12:175764
|
C | T | 63 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(60): Show | 134 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*731C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 731 | chr12 | 175764 | |||||
| chr12:175861
|
C | A | 70 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(67): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*828C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 828 | chr12 | 175861 | |||||
| chr12:175873
|
G | A | 1 | a0020c0047t0042 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*840G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 840 | chr12 | 175873 | |||||
| chr12:175944
|
C | T | 7 | a0001c0003t0005a0001c0003t0012a0001c0004t0012others(4): Show | 13 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*911C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 911 | chr12 | 175944 | |||||
| chr12:175962
|
AGCCCGAG others(27): Show |
A | 7 | a0001c0003t0005a0001c0003t0012a0001c0004t0012others(4): Show | 13 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*959_*992delGCTCGG others(28): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 959 | INFO_REALIGN_3_PRIME | chr12 | 175962 | ||||
| chr12:176149
|
AC | A | 10 | a0001c0003t0005a0001c0003t0012a0001c0004t0012others(7): Show | 17 | HG02055.hp1 HG02055.hp2 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1124delC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1124 | INFO_REALIGN_3_PRIME | chr12 | 176149 | ||||
| chr12:176278
|
G | C | 2 | a0001c0002t0043a0001c0002t0044 | 2 | HG02027.hp1 NA18973.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1245G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1245 | chr12 | 176278 | |||||
| chr12:176313
|
C | T | 5 | a0001c0033t0013a0002c0001t0013a0002c0015t0013others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1280C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1280 | chr12 | 176313 | |||||
| chr12:176360
|
G | A | 2 | a0003c0010t0015a0003c0017t0015 | 3 | HG01106.hp1 HG03471.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1327G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1327 | chr12 | 176360 | |||||
| chr12:176620
|
TTGTG | T | 5 | a0001c0003t0005a0002c0001t0005a0003c0005t0019others(2): Show | 10 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1602_*1605delTGTG | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1602 | INFO_REALIGN_3_PRIME | chr12 | 176620 | ||||
| chr12:176728
|
G | A | 4 | a0001c0003t0012a0001c0004t0012a0003c0005t0012others(1): Show | 5 | HG02055.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1695G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1695 | chr12 | 176728 | |||||
| chr12:176772
|
T | C | 7 | a0001c0003t0007a0003c0010t0007a0003c0045t0045others(4): Show | 9 | HG00597.hp2 HG01358.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1739T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1739 | chr12 | 176772 | |||||
| chr12:176808
|
T | C | 1 | a0002c0015t0046 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1775T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1775 | chr12 | 176808 | |||||
| chr12:176953
|
G | A | 1 | a0006c0012t0032 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 1920 | chr12 | 176953 | |||||
| chr12:177087
|
G | A | 1 | a0001c0003t0033 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2054 | chr12 | 177087 | |||||
| chr12:177126
|
C | CCAGGCAG others(43): Show |
1 | a0001c0004t0035 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2132_*2181dupACTT others(46): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2182 | INFO_REALIGN_3_PRIME | chr12 | 177126 | ||||
| chr12:177126
|
C | CCAGGCAG others(29): Show |
3 | a0001c0003t0005a0002c0001t0005a0006c0012t0005 | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2101_*2102insTCAC others(32): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2102 | INFO_REALIGN_3_PRIME | chr12 | 177126 | ||||
| chr12:177126
|
CCAGGCAG others(43): Show |
C | 4 | a0001c0003t0012a0001c0004t0012a0003c0005t0012others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2132_*2181delACTT others(46): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2132 | INFO_REALIGN_3_PRIME | chr12 | 177126 | ||||
| chr12:177126
|
CCAGGCAG others(143): Show |
C | 1 | a0001c0002t0055 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2142_*2291del | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2142 | INFO_REALIGN_3_PRIME | chr12 | 177126 | ||||
| chr12:177134
|
GACCCCGT others(93): Show |
G | 20 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(17): Show | 75 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2132_*2231delACTT others(96): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2132 | INFO_REALIGN_3_PRIME | chr12 | 177134 | ||||
| chr12:177165
|
A | ACTTACCA others(43): Show |
5 | a0002c0001t0020a0002c0015t0031a0003c0010t0015others(2): Show | 6 | HG01106.hp1 HG01884.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2151_*2200dupGACC others(46): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2201 | INFO_REALIGN_3_PRIME | chr12 | 177165 | ||||
| chr12:177165
|
A | G | 11 | a0001c0003t0005a0001c0003t0007a0001c0004t0012others(8): Show | 18 | HG00673.hp2 HG01358.hp2 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2132A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2132 | chr12 | 177165 | |||||
| chr12:177165
|
ACTTACCA others(43): Show |
A | 1 | a0001c0019t0034 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2151_*2200delGACC others(46): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2151 | INFO_REALIGN_3_PRIME | chr12 | 177165 | ||||
| chr12:177165
|
ACTTACCA others(93): Show |
A | 1 | a0017c0053t0026 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2182_*2281delGCTT others(96): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2182 | INFO_REALIGN_3_PRIME | chr12 | 177165 | ||||
| chr12:177184
|
GACCCCGT others(43): Show |
G | 20 | a0001c0003t0004a0001c0004t0004a0001c0004t0012others(17): Show | 29 | HG00733.hp1 HG01243.hp1 HG01496.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2201_*2250delAACC others(46): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2201 | INFO_REALIGN_3_PRIME | chr12 | 177184 | ||||
| chr12:177234
|
A | G | 44 | a0001c0003t0005a0001c0003t0007a0001c0003t0010others(41): Show | 61 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2201A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2201 | chr12 | 177234 | |||||
| chr12:177315
|
A | G | 29 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(26): Show | 85 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2282A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2282 | chr12 | 177315 | |||||
| chr12:177325
|
T | G | 1 | a0002c0001t0036 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2292T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2292 | chr12 | 177325 | |||||
| chr12:177332
|
T | A | 22 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(19): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2299T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2299 | chr12 | 177332 | |||||
| chr12:177333
|
C | A | 22 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(19): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2300C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2300 | chr12 | 177333 | |||||
| chr12:177334
|
CCCTGTTG | C | 22 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(19): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2302_*2308delCCTG others(3): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2302 | chr12 | 177334 | |||||
| chr12:177346
|
C | G | 22 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(19): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2313C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2313 | chr12 | 177346 | |||||
| chr12:177348
|
C | G | 22 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(19): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2315C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2315 | chr12 | 177348 | |||||
| chr12:177463
|
A | G | 2 | a0003c0005t0019a0003c0010t0019 | 2 | HG02922.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2430A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2430 | chr12 | 177463 | |||||
| chr12:177580
|
C | T | 10 | a0001c0003t0005a0001c0003t0012a0001c0004t0012others(7): Show | 17 | HG02055.hp1 HG02055.hp2 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2547C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2547 | chr12 | 177580 | |||||
| chr12:177583
|
T | C | 1 | a0004c0008t0053 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2550T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2550 | chr12 | 177583 | |||||
| chr12:177589
|
G | A | 1 | a0002c0040t0029 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2556G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2556 | chr12 | 177589 | |||||
| chr12:177605
|
G | A | 3 | a0001c0003t0010a0001c0006t0010a0007c0050t0010 | 5 | HG00280.hp1 HG01074.hp2 HG01516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2572G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2572 | chr12 | 177605 | |||||
| chr12:177632
|
G | T | 3 | a0002c0001t0020a0002c0015t0031a0003c0010t0020 | 3 | HG01884.hp2 HG02896.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2599G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2599 | chr12 | 177632 | |||||
| chr12:177637
|
T | G | 1 | a0001c0004t0037 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2604T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2604 | chr12 | 177637 | |||||
| chr12:177663
|
C | T | 3 | a0001c0004t0016a0002c0001t0016a0023c0039t0030 | 4 | HG00280.hp2 HG01243.hp2 HG01258.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2630C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2630 | chr12 | 177663 | |||||
| chr12:177666
|
T | G | 2 | a0003c0010t0015a0003c0017t0015 | 3 | HG01106.hp1 HG03471.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2633T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2633 | chr12 | 177666 | |||||
| chr12:177667
|
G | A | 1 | a0025c0027t0038 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2634G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2634 | chr12 | 177667 | |||||
| chr12:177667
|
G | C | 1 | a0001c0004t0060 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2634G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2634 | chr12 | 177667 | |||||
| chr12:177805
|
C | T | 3 | a0002c0001t0020a0002c0015t0031a0003c0010t0020 | 3 | HG01884.hp2 HG02896.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2772C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2772 | chr12 | 177805 | |||||
| chr12:177847
|
TG | T | 6 | a0001c0003t0011a0001c0004t0011a0001c0037t0011others(3): Show | 8 | HG01106.hp1 HG03017.hp2 HG03471.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2820delG | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2820 | INFO_REALIGN_3_PRIME | chr12 | 177847 | ||||
| chr12:177934
|
C | T | 1 | a0002c0015t0046 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2901C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2901 | chr12 | 177934 | |||||
| chr12:177997
|
G | A | 2 | a0002c0001t0008a0005c0018t0008 | 7 | HG01074.hp1 HG01358.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2964G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 2964 | chr12 | 177997 | |||||
| chr12:178088
|
C | A | 1 | a0001c0002t0047 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3055C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3055 | chr12 | 178088 | |||||
| chr12:178106
|
AGCCT | A | 60 | a0001c0002t0003a0001c0002t0048a0001c0003t0004others(57): Show | 94 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*3089_*3092delTGCC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3089 | INFO_REALIGN_3_PRIME | chr12 | 178106 | ||||
| chr12:178174
|
C | G | 3 | a0001c0003t0005a0002c0001t0005a0006c0012t0005 | 8 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3141C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3141 | chr12 | 178174 | |||||
| chr12:178178
|
C | T | 1 | a0001c0002t0044 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3145C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3145 | chr12 | 178178 | |||||
| chr12:178179
|
G | A | 6 | a0001c0004t0016a0001c0004t0058a0002c0001t0016others(3): Show | 7 | HG01243.hp2 HG01258.hp1 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3146G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3146 | chr12 | 178179 | |||||
| chr12:178192
|
C | T | 5 | a0002c0001t0006a0004c0011t0006a0012c0023t0017others(2): Show | 10 | HG00438.hp2 NA18943.hp2 NA18944.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3159C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3159 | chr12 | 178192 | |||||
| chr12:178196
|
A | G | 1 | a0024c0036t0057 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3163A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3163 | chr12 | 178196 | |||||
| chr12:178200
|
GTC | G | 33 | a0001c0003t0004a0001c0003t0011a0001c0003t0012others(30): Show | 46 | HG00733.hp1 HG01106.hp1 HG01243.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3171_*3172delCT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3171 | INFO_REALIGN_3_PRIME | chr12 | 178200 | ||||
| chr12:178234
|
ATCTG | A | 6 | a0001c0003t0011a0001c0004t0011a0001c0037t0011others(3): Show | 8 | HG01106.hp1 HG03017.hp2 HG03471.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3208_*3211delTGTC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3208 | INFO_REALIGN_3_PRIME | chr12 | 178234 | ||||
| chr12:178253
|
T | A | 4 | a0001c0003t0011a0001c0004t0011a0001c0037t0011others(1): Show | 5 | HG03017.hp2 HG03831.hp1 HG04115.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3220T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3220 | chr12 | 178253 | |||||
| chr12:178279
|
A | T | 2 | a0001c0004t0058a0003c0005t0059 | 2 | HG00735.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3246A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3246 | chr12 | 178279 | |||||
| chr12:178306
|
TGA | T | 22 | a0001c0002t0002a0001c0002t0043a0001c0002t0044others(19): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3282_*3283delGA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3282 | INFO_REALIGN_3_PRIME | chr12 | 178306 | ||||
| chr12:178307
|
G | A | 45 | a0001c0003t0004a0001c0003t0005a0001c0003t0007others(42): Show | 64 | HG00597.hp2 HG00733.hp1 HG01243.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3274G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 14/14 | 3274 | chr12 | 178307 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:67449
|
A | G | 7 | a0001c0004t0001g0277a0003c0005t0009g0281a0012c0023t0017g0280others(4): Show | 7 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.554+13A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67449 | ||||||
| chr12:67468
|
G | C | 1 | a0010c0014t0003g0002 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.554+32G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67468 | ||||||
| chr12:67492
|
G | A | 1 | a0017c0053t0026g0275 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.554+56G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67492 | ||||||
| chr12:67521
|
C | G | 4 | a0011c0055t0018g0271a0011c0058t0027g0272a0015c0056t0017g0273others(1): Show | 4 | HG00733.hp2 HG01175.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+85C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67521 | ||||||
| chr12:67575
|
A | G | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.554+139A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67575 | ||||||
| chr12:67670
|
G | A | 30 | a0001c0002t0002g0008a0001c0003t0007g0003a0001c0003t0007g0004others(27): Show | 30 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.554+234G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67670 | ||||||
| chr12:67685
|
G | A | 80 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0002t0002g0039others(77): Show | 80 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(77): Show |
intron_variant | MODIFIER | c.554+249G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67685 | ||||||
| chr12:67886
|
G | A | 1 | a0012c0023t0018g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.554+450G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67886 | ||||||
| chr12:67897
|
G | A | 4 | a0011c0055t0018g0271a0011c0058t0027g0272a0015c0056t0017g0273others(1): Show | 4 | HG00733.hp2 HG01175.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+461G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67897 | ||||||
| chr12:67950
|
G | A | 2 | a0001c0024t0001g0032a0003c0005t0003g0033 | 2 | HG01123.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.554+514G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 67950 | ||||||
| chr12:68033
|
G | T | 4 | a0011c0055t0018g0271a0011c0058t0027g0272a0015c0056t0017g0273others(1): Show | 4 | HG00733.hp2 HG01175.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+597G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68033 | ||||||
| chr12:68068
|
A | G | 1 | a0002c0001t0020g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.554+632A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68068 | ||||||
| chr12:68235
|
A | AG | 6 | a0001c0002t0002g0066a0001c0004t0002g0070a0002c0001t0008g0067others(3): Show | 6 | HG02109.hp2 HG03098.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+801dupG | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 68235 | |||||
| chr12:68249
|
T | C | 1 | a0001c0004t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.554+813T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68249 | ||||||
| chr12:68251
|
C | T | 1 | a0012c0023t0018g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.554+815C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68251 | ||||||
| chr12:68346
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+910T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68346 | ||||||
| chr12:68415
|
C | T | 2 | a0002c0001t0009g0064a0006c0012t0004g0065 | 2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+979C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68415 | ||||||
| chr12:68559
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+1123T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68559 | ||||||
| chr12:68599
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+1163C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68599 | ||||||
| chr12:68602
|
A | G | 11 | a0001c0003t0002g0060a0001c0004t0001g0053a0001c0043t0004g0063others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.554+1166A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68602 | ||||||
| chr12:68657
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+1221G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68657 | ||||||
| chr12:68830
|
G | A | 6 | a0003c0005t0009g0281a0012c0023t0017g0280a0012c0023t0018g0276others(3): Show | 6 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+1394G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68830 | ||||||
| chr12:68835
|
T | C | 3 | a0001c0041t0056g0072a0003c0005t0012g0074a0003c0005t0062g0073 | 3 | HG01952.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.554+1399T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 68835 | ||||||
| chr12:69081
|
T | C | 14 | a0001c0002t0002g0008a0001c0003t0007g0003a0001c0003t0007g0004others(11): Show | 14 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.554+1645T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69081 | ||||||
| chr12:69188
|
G | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+1752G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69188 | ||||||
| chr12:69291
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+1855A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69291 | ||||||
| chr12:69293
|
C | G | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+1857C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69293 | ||||||
| chr12:69294
|
C | T | 1 | a0001c0004t0002g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.554+1858C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69294 | ||||||
| chr12:69305
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+1869C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69305 | ||||||
| chr12:69344
|
C | A | 6 | a0001c0007t0001g0075a0012c0023t0017g0280a0012c0023t0018g0276others(3): Show | 6 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+1908C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69344 | ||||||
| chr12:69345
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+1909G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69345 | ||||||
| chr12:69386
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+1950T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69386 | ||||||
| chr12:69417
|
T | C | 10 | a0001c0004t0001g0277a0011c0055t0018g0271a0011c0058t0027g0272others(7): Show | 10 | HG00733.hp2 HG01175.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+1981T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69417 | ||||||
| chr12:69480
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2044A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69480 | ||||||
| chr12:69562
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2126C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69562 | ||||||
| chr12:69586
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2150C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69586 | ||||||
| chr12:69606
|
T | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2170T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69606 | ||||||
| chr12:69616
|
T | C | 72 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0002t0002g0039others(69): Show | 72 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.554+2180T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69616 | ||||||
| chr12:69623
|
C | T | 1 | a0002c0001t0008g0025 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.554+2187C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69623 | ||||||
| chr12:69644
|
T | C | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+2208T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69644 | ||||||
| chr12:69670
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2234C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69670 | ||||||
| chr12:69677
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2241G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69677 | ||||||
| chr12:69804
|
A | C | 1 | a0002c0009t0002g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.554+2368A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69804 | ||||||
| chr12:69813
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2377G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69813 | ||||||
| chr12:69834
|
G | A | 2 | a0003c0005t0009g0077a0003c0010t0020g0078 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.554+2398G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69834 | ||||||
| chr12:69877
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2441T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69877 | ||||||
| chr12:69911
|
C | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2475C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69911 | ||||||
| chr12:69943
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2507G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69943 | ||||||
| chr12:69963
|
G | A | 5 | a0001c0002t0002g0035a0002c0001t0022g0038a0003c0005t0013g0036others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2527G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69963 | ||||||
| chr12:69981
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2545C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69981 | ||||||
| chr12:69997
|
C | T | 10 | a0001c0004t0001g0277a0011c0055t0018g0271a0011c0058t0027g0272others(7): Show | 10 | HG00733.hp2 HG01175.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+2561C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 69997 | ||||||
| chr12:70030
|
C | T | 3 | a0002c0001t0005g0014a0006c0012t0005g0016a0008c0016t0061g0015 | 3 | HG02280.hp2 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.554+2594C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70030 | ||||||
| chr12:70061
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2625A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70061 | ||||||
| chr12:70107
|
C | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2671C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70107 | ||||||
| chr12:70123
|
GA | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2688delA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70123 | ||||||
| chr12:70244
|
C | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2808C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70244 | ||||||
| chr12:70266
|
T | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2830T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70266 | ||||||
| chr12:70273
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2837G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70273 | ||||||
| chr12:70303
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2867A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70303 | ||||||
| chr12:70313
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2877C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70313 | ||||||
| chr12:70325
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2889A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70325 | ||||||
| chr12:70404
|
T | C | 5 | a0001c0002t0002g0066a0001c0004t0002g0070a0002c0001t0008g0067others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+2968T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70404 | ||||||
| chr12:70420
|
C | A | 2 | a0001c0003t0012g0049a0024c0036t0057g0048 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.554+2984C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70420 | ||||||
| chr12:70420
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2984C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70420 | ||||||
| chr12:70422
|
G | C | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.554+2986G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70422 | ||||||
| chr12:70424
|
G | C | 1 | a0004c0008t0003g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.554+2988G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70424 | ||||||
| chr12:70503
|
C | T | 4 | a0012c0023t0017g0280a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01975.hp1 HG02056.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+3067C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70503 | ||||||
| chr12:70550
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3114C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70550 | ||||||
| chr12:70562
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3126A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70562 | ||||||
| chr12:70572
|
AC | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3137delC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70572 | ||||||
| chr12:70677
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3241T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70677 | ||||||
| chr12:70678
|
G | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3242G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70678 | ||||||
| chr12:70750
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3314G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70750 | ||||||
| chr12:70811
|
C | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3375C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70811 | ||||||
| chr12:70871
|
C | G | 1 | a0004c0008t0003g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.554+3435C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70871 | ||||||
| chr12:70904
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3468C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70904 | ||||||
| chr12:70951
|
A | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3515A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70951 | ||||||
| chr12:70969
|
A | G | 1 | a0001c0004t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.554+3533A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 70969 | ||||||
| chr12:71017
|
C | T | 9 | a0001c0003t0002g0060a0001c0004t0001g0053a0002c0001t0005g0054others(6): Show | 9 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.554+3581C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71017 | ||||||
| chr12:71019
|
T | C | 30 | a0001c0002t0002g0008a0001c0003t0007g0003a0001c0003t0007g0004others(27): Show | 30 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.554+3583T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71019 | ||||||
| chr12:71053
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3617T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71053 | ||||||
| chr12:71110
|
C | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3674C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71110 | ||||||
| chr12:71118
|
T | A | 280 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.554+3682T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71118 | ||||||
| chr12:71156
|
T | C | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.554+3720T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71156 | ||||||
| chr12:71167
|
T | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3731T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71167 | ||||||
| chr12:71185
|
G | A | 2 | a0001c0003t0012g0049a0024c0036t0057g0048 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.554+3749G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71185 | ||||||
| chr12:71189
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3753A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71189 | ||||||
| chr12:71306
|
C | A | 1 | a0001c0004t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.554+3870C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71306 | ||||||
| chr12:71311
|
T | C | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.554+3875T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71311 | ||||||
| chr12:71316
|
C | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3880C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71316 | ||||||
| chr12:71321
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3885G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71321 | ||||||
| chr12:71378
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3942T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71378 | ||||||
| chr12:71379
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3943G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71379 | ||||||
| chr12:71435
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+3999T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71435 | ||||||
| chr12:71512
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4076A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71512 | ||||||
| chr12:71535
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4099C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71535 | ||||||
| chr12:71622
|
C | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4186C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71622 | ||||||
| chr12:71670
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4234T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71670 | ||||||
| chr12:71690
|
C | T | 1 | a0003c0010t0007g0268 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.554+4254C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71690 | ||||||
| chr12:71818
|
T | G | 5 | a0001c0004t0001g0277a0011c0055t0018g0271a0011c0058t0027g0272others(2): Show | 5 | HG00733.hp2 HG01175.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4382T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71818 | ||||||
| chr12:71845
|
G | A | 3 | a0001c0004t0003g0082a0002c0009t0002g0080a0002c0009t0002g0081 | 3 | HG01517.hp1 HG02273.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.554+4409G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71845 | ||||||
| chr12:71857
|
A | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4421A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71857 | ||||||
| chr12:71908
|
G | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4472G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71908 | ||||||
| chr12:71923
|
G | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4487G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71923 | ||||||
| chr12:71985
|
C | G | 1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.554+4549C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71985 | ||||||
| chr12:71990
|
C | T | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4554C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 71990 | ||||||
| chr12:72050
|
A | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4614A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72050 | ||||||
| chr12:72100
|
C | G | 62 | a0001c0002t0002g0001a0001c0002t0002g0218a0001c0002t0002g0239others(59): Show | 63 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.554+4664C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72100 | ||||||
| chr12:72109
|
T | C | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4673T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72109 | ||||||
| chr12:72200
|
C | G | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+4764C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72200 | ||||||
| chr12:72274
|
C | T | 92 | a0001c0002t0002g0001a0001c0002t0002g0066a0001c0002t0002g0218others(89): Show | 93 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.554+4838C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72274 | ||||||
| chr12:72294
|
C | A | 9 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(6): Show | 9 | HG01074.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+4858C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72294 | ||||||
| chr12:72310
|
A | G | 11 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(8): Show | 11 | HG01243.hp1 HG01358.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+4874A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72310 | ||||||
| chr12:72333
|
T | TAAAAAAG others(348): Show |
1 | a0001c0003t0001g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.554+4913_554+4914i others(357): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 72333 | |||||
| chr12:72364
|
A | G | 97 | a0001c0002t0002g0001a0001c0002t0002g0066a0001c0002t0002g0218others(94): Show | 98 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.554+4928A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72364 | ||||||
| chr12:72365
|
G | A | 1 | a0002c0001t0005g0014 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.554+4929G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72365 | ||||||
| chr12:72408
|
C | T | 1 | a0001c0004t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.554+4972C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72408 | ||||||
| chr12:72507
|
T | TGGCAGCT others(72): Show |
5 | a0002c0001t0024g0017a0011c0055t0018g0271a0011c0058t0027g0272others(2): Show | 5 | HG00733.hp2 HG01175.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+5123_554+5124i others(81): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 72507 | |||||
| chr12:72507
|
T | TGGCAGCT others(72): Show |
92 | a0001c0002t0002g0001a0001c0002t0002g0066a0001c0002t0002g0218others(89): Show | 93 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.554+5123_554+5124i others(81): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 72507 | |||||
| chr12:72560
|
A | G | 10 | a0001c0004t0001g0277a0001c0004t0012g0021a0001c0004t0012g0022others(7): Show | 10 | HG01070.hp1 HG01074.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.554+5124A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72560 | ||||||
| chr12:72574
|
C | T | 5 | a0001c0002t0002g0205a0001c0002t0047g0201a0001c0003t0001g0204others(2): Show | 5 | HG01257.hp1 HG01257.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+5138C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72574 | ||||||
| chr12:72575
|
A | AGAGGTGA others(72): Show |
19 | a0001c0004t0001g0277a0001c0004t0004g0031a0001c0004t0012g0021others(16): Show | 19 | HG01070.hp1 HG01074.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.554+5150_554+5151i others(81): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 72575 | |||||
| chr12:72575
|
A | G | 225 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0066others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.554+5139A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72575 | ||||||
| chr12:72843
|
G | A | 1 | a0001c0007t0001g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.554+5407G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72843 | ||||||
| chr12:72852
|
A | G | 1 | a0001c0004t0011g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.554+5416A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72852 | ||||||
| chr12:72861
|
G | A | 3 | a0001c0034t0001g0214a0002c0009t0002g0213a0004c0008t0001g0212 | 3 | HG00438.hp1 HG02080.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.554+5425G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72861 | ||||||
| chr12:72914
|
C | T | 1 | a0001c0003t0001g0267 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.554+5478C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72914 | ||||||
| chr12:72915
|
G | A | 1 | a0002c0001t0003g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.554+5479G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72915 | ||||||
| chr12:72918
|
C | T | 1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.554+5482C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72918 | ||||||
| chr12:72959
|
T | C | 2 | a0001c0002t0044g0084a0002c0001t0006g0085 | 2 | HG02027.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.554+5523T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72959 | ||||||
| chr12:72962
|
C | T | 2 | a0001c0004t0003g0197a0001c0004t0003g0198 | 2 | NA19010.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.554+5526C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72962 | ||||||
| chr12:72984
|
T | G | 19 | a0001c0002t0002g0008a0001c0003t0007g0003a0001c0003t0007g0004others(16): Show | 19 | HG01167.hp1 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+5548T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 72984 | ||||||
| chr12:73010
|
T | C | 1 | a0002c0001t0003g0216 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.554+5574T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73010 | ||||||
| chr12:73040
|
T | C | 237 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0066others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.554+5604T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73040 | ||||||
| chr12:73049
|
T | A | 5 | a0012c0023t0017g0280a0012c0023t0018g0276a0017c0053t0026g0275others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+5613T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73049 | ||||||
| chr12:73049
|
T | TATAA | 10 | a0001c0002t0002g0261a0001c0006t0002g0258a0002c0001t0002g0047others(7): Show | 10 | HG00323.hp1 HG01081.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.554+5659_554+5662d others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73049 | |||||
| chr12:73049
|
TATAA | T | 21 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0225others(18): Show | 21 | HG00438.hp1 HG01070.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.554+5659_554+5662d others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73049 | |||||
| chr12:73049
|
TATAAATA others(1): Show |
T | 5 | a0002c0009t0002g0222a0003c0005t0009g0281a0004c0008t0001g0212others(2): Show | 5 | HG00735.hp2 HG02080.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+5655_554+5662d others(10): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73049 | |||||
| chr12:73049
|
TATAAATA others(5): Show |
T | 22 | a0001c0002t0002g0179a0001c0002t0002g0182a0001c0002t0002g0186others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(19): Show |
intron_variant | MODIFIER | c.554+5651_554+5662d others(14): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73049 | |||||
| chr12:73049
|
TATAAATA others(9): Show |
T | 119 | a0001c0002t0002g0039a0001c0002t0002g0090a0001c0002t0002g0096others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.554+5647_554+5662d others(18): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73049 | |||||
| chr12:73049
|
TATAAATA others(13): Show |
T | 7 | a0001c0003t0001g0086a0001c0004t0004g0031a0002c0001t0022g0087others(4): Show | 7 | HG00733.hp2 HG01175.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.554+5643_554+5662d others(22): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73049 | |||||
| chr12:73049
|
TATAAATA others(17): Show |
T | 5 | a0001c0004t0035g0030a0002c0001t0004g0027a0002c0001t0004g0028others(2): Show | 5 | HG01243.hp1 HG01358.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+5639_554+5662d others(26): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73049 | |||||
| chr12:73072
|
A | T | 1 | a0018c0054t0014g0279 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.554+5636A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73072 | ||||||
| chr12:73076
|
A | T | 2 | a0012c0023t0017g0280a0018c0054t0014g0279 | 2 | HG01975.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.554+5640A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73076 | ||||||
| chr12:73080
|
A | T | 4 | a0012c0023t0017g0280a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01975.hp1 HG02056.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+5644A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73080 | ||||||
| chr12:73083
|
TAAATAAA others(9): Show |
T | 1 | a0001c0006t0002g0196 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.554+5650_554+5665d others(18): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73083 | |||||
| chr12:73084
|
A | T | 4 | a0012c0023t0017g0280a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01975.hp1 HG02056.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+5648A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73084 | ||||||
| chr12:73088
|
A | T | 4 | a0012c0023t0017g0280a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01975.hp1 HG02056.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+5652A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73088 | ||||||
| chr12:73091
|
TAAATAAA others(1): Show |
T | 6 | a0002c0001t0008g0052a0002c0001t0022g0038a0003c0010t0015g0263others(3): Show | 6 | HG01106.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+5658_554+5665d others(10): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73091 | |||||
| chr12:73095
|
T | A | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+5659T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73095 | ||||||
| chr12:73098
|
A | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+5662A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73098 | ||||||
| chr12:73175
|
C | T | 3 | a0017c0053t0026g0275a0018c0054t0014g0279a0019c0052t0014g0278 | 3 | HG01975.hp1 HG02056.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.554+5739C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73175 | ||||||
| chr12:73192
|
AGAT | A | 133 | a0001c0002t0002g0039a0001c0002t0002g0090a0001c0002t0002g0096others(130): Show | 133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.554+5758_554+5760d others(5): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73192 | |||||
| chr12:73266
|
C | T | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+5830C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73266 | ||||||
| chr12:73285
|
C | A | 2 | a0001c0024t0001g0032a0003c0005t0003g0033 | 2 | HG01123.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.554+5849C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73285 | ||||||
| chr12:73297
|
G | C | 1 | a0001c0004t0001g0053 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.554+5861G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73297 | ||||||
| chr12:73341
|
TGTC | T | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+5908_554+5910d others(5): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73341 | |||||
| chr12:73344
|
C | T | 9 | a0001c0003t0002g0060a0001c0004t0001g0053a0002c0001t0005g0054others(6): Show | 9 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.554+5908C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73344 | ||||||
| chr12:73353
|
G | T | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+5917G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73353 | ||||||
| chr12:73445
|
T | TG | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+6011dupG | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73445 | |||||
| chr12:73656
|
C | T | 2 | a0012c0023t0018g0276a0015c0056t0017g0273 | 2 | HG01361.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.554+6220C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73656 | ||||||
| chr12:73667
|
GA | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+6232delA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73667 | ||||||
| chr12:73669
|
C | A | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.554+6233C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73669 | ||||||
| chr12:73673
|
A | C | 9 | a0001c0004t0001g0277a0011c0055t0018g0271a0011c0058t0027g0272others(6): Show | 9 | HG00733.hp2 HG01175.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+6237A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73673 | ||||||
| chr12:73676
|
A | AAAAAAG | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0024t0001g0032others(7): Show | 10 | HG01074.hp1 HG01123.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.554+6262_554+6267d others(8): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 73676 | |||||
| chr12:73709
|
G | A | 6 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0007t0001g0042others(3): Show | 6 | HG01993.hp1 HG02015.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+6273G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73709 | ||||||
| chr12:73725
|
A | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+6289A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73725 | ||||||
| chr12:73794
|
G | A | 1 | a0003c0046t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.554+6358G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73794 | ||||||
| chr12:73816
|
A | G | 2 | a0002c0001t0024g0177a0003c0010t0019g0178 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.554+6380A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73816 | ||||||
| chr12:73854
|
A | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+6418A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73854 | ||||||
| chr12:73870
|
C | A | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.554+6434C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73870 | ||||||
| chr12:73937
|
G | A | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+6501G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73937 | ||||||
| chr12:73938
|
G | T | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+6502G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73938 | ||||||
| chr12:73972
|
A | C | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+6536A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 73972 | ||||||
| chr12:74247
|
A | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+6811A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74247 | ||||||
| chr12:74346
|
G | T | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+6910G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74346 | ||||||
| chr12:74347
|
A | C | 1 | a0001c0003t0001g0176 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.554+6911A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74347 | ||||||
| chr12:74347
|
A | T | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+6911A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74347 | ||||||
| chr12:74402
|
A | G | 2 | a0001c0043t0004g0063a0014c0028t0001g0062 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.554+6966A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74402 | ||||||
| chr12:74470
|
C | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7034C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74470 | ||||||
| chr12:74562
|
C | T | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7126C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74562 | ||||||
| chr12:74612
|
C | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7176C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74612 | ||||||
| chr12:74635
|
C | T | 1 | a0008c0016t0061g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.554+7199C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74635 | ||||||
| chr12:74651
|
G | A | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7215G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74651 | ||||||
| chr12:74742
|
T | C | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7306T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74742 | ||||||
| chr12:74757
|
G | A | 6 | a0001c0041t0056g0072a0002c0015t0031g0207a0003c0005t0009g0077others(3): Show | 6 | HG01884.hp2 HG01952.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+7321G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74757 | ||||||
| chr12:74789
|
C | A | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7353C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74789 | ||||||
| chr12:74798
|
G | A | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7362G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74798 | ||||||
| chr12:74804
|
C | T | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+7368C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74804 | ||||||
| chr12:74829
|
C | T | 2 | a0002c0001t0009g0064a0006c0012t0004g0065 | 2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+7393C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74829 | ||||||
| chr12:74857
|
A | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7421A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74857 | ||||||
| chr12:74912
|
A | G | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7476A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74912 | ||||||
| chr12:74936
|
T | C | 4 | a0012c0023t0018g0276a0017c0053t0026g0275a0018c0054t0014g0279others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+7500T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74936 | ||||||
| chr12:74956
|
G | C | 3 | a0012c0023t0018g0276a0018c0054t0014g0279a0019c0052t0014g0278 | 3 | HG01361.hp2 HG01975.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.554+7520G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 74956 | ||||||
| chr12:75019
|
C | T | 3 | a0012c0023t0018g0276a0018c0054t0014g0279a0019c0052t0014g0278 | 3 | HG01361.hp2 HG01975.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.554+7583C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75019 | ||||||
| chr12:75027
|
C | G | 9 | a0001c0003t0002g0060a0001c0004t0001g0053a0002c0001t0005g0054others(6): Show | 9 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.554+7591C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75027 | ||||||
| chr12:75069
|
G | C | 3 | a0012c0023t0018g0276a0018c0054t0014g0279a0019c0052t0014g0278 | 3 | HG01361.hp2 HG01975.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.554+7633G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75069 | ||||||
| chr12:75084
|
A | G | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.554+7648A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75084 | ||||||
| chr12:75130
|
C | A | 3 | a0012c0023t0018g0276a0018c0054t0014g0279a0019c0052t0014g0278 | 3 | HG01361.hp2 HG01975.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.554+7694C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75130 | ||||||
| chr12:75147
|
T | C | 12 | a0001c0003t0002g0060a0001c0004t0001g0053a0002c0001t0005g0054others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+7711T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75147 | ||||||
| chr12:75153
|
T | C | 3 | a0012c0023t0018g0276a0018c0054t0014g0279a0019c0052t0014g0278 | 3 | HG01361.hp2 HG01975.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.554+7717T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75153 | ||||||
| chr12:75192
|
A | G | 1 | a0001c0003t0001g0267 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.554+7756A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75192 | ||||||
| chr12:75232
|
G | T | 5 | a0001c0024t0001g0032a0003c0005t0003g0033a0012c0023t0018g0276others(2): Show | 5 | HG01123.hp2 HG01361.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+7796G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75232 | ||||||
| chr12:75238
|
C | A | 62 | a0001c0002t0002g0001a0001c0002t0002g0218a0001c0002t0002g0239others(59): Show | 63 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.554+7802C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75238 | ||||||
| chr12:75303
|
A | T | 12 | a0001c0003t0002g0060a0001c0004t0001g0053a0002c0001t0005g0054others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+7867A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75303 | ||||||
| chr12:75311
|
A | C | 1 | a0002c0001t0006g0175 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.554+7875A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75311 | ||||||
| chr12:75342
|
G | A | 9 | a0001c0003t0002g0060a0001c0004t0001g0053a0002c0001t0005g0054others(6): Show | 9 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.554+7906G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75342 | ||||||
| chr12:75365
|
G | A | 1 | a0001c0004t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.554+7929G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75365 | ||||||
| chr12:75394
|
G | A | 2 | a0002c0001t0009g0064a0006c0012t0004g0065 | 2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+7958G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75394 | ||||||
| chr12:75652
|
C | T | 3 | a0012c0023t0018g0276a0018c0054t0014g0279a0019c0052t0014g0278 | 3 | HG01361.hp2 HG01975.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.554+8216C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75652 | ||||||
| chr12:75710
|
AATACTGG others(8): Show |
A | 1 | a0019c0052t0014g0278 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.554+8278_554+8292d others(17): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 75710 | |||||
| chr12:75737
|
G | A | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8301G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75737 | ||||||
| chr12:75882
|
C | G | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8446C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75882 | ||||||
| chr12:75883
|
T | A | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8447T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75883 | ||||||
| chr12:75886
|
C | A | 2 | a0011c0055t0018g0271a0016c0057t0014g0274 | 2 | HG00733.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.554+8450C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75886 | ||||||
| chr12:75892
|
T | C | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8456T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75892 | ||||||
| chr12:75897
|
T | C | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8461T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 75897 | ||||||
| chr12:76013
|
T | C | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+8577T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76013 | ||||||
| chr12:76032
|
C | G | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8596C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76032 | ||||||
| chr12:76034
|
C | T | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+8598C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76034 | ||||||
| chr12:76044
|
A | G | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8608A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76044 | ||||||
| chr12:76086
|
TCA | T | 18 | a0001c0002t0002g0035a0001c0002t0002g0167a0001c0003t0002g0169others(15): Show | 18 | HG00735.hp1 HG01081.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.554+8695_554+8696d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76086
|
TCACA | T | 43 | a0001c0003t0001g0157a0001c0003t0001g0206a0001c0003t0005g0193others(40): Show | 43 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.554+8693_554+8696d others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76086
|
TCACACA | T | 18 | a0001c0002t0002g0001a0001c0003t0001g0141a0001c0003t0002g0187others(15): Show | 19 | HG00642.hp2 HG00733.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+8691_554+8696d others(8): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76086
|
TCACACAC others(1): Show |
T | 95 | a0001c0002t0002g0096a0001c0002t0002g0098a0001c0002t0002g0099others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.554+8689_554+8696d others(10): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76086
|
TCACACAC others(3): Show |
T | 79 | a0001c0002t0002g0008a0001c0002t0002g0066a0001c0002t0002g0090others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.554+8687_554+8696d others(12): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76086
|
TCACACAC others(5): Show |
T | 2 | a0002c0001t0020g0071a0007c0021t0001g0230 | 2 | HG03453.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.554+8685_554+8696d others(14): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76086
|
TCACACAC others(9): Show |
T | 3 | a0001c0002t0002g0179a0001c0003t0001g0088a0003c0017t0002g0089 | 3 | HG00408.hp2 HG02040.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.554+8681_554+8696d others(18): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76086
|
TCACACAC others(13): Show |
T | 1 | a0018c0054t0014g0279 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.554+8677_554+8696d others(22): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76086
|
TCACACAC others(15): Show |
T | 1 | a0012c0023t0018g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.554+8675_554+8696d others(24): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76086 | |||||
| chr12:76090
|
A | C | 8 | a0001c0002t0002g0039a0001c0003t0001g0044a0001c0003t0001g0045others(5): Show | 8 | HG01993.hp1 HG02015.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.554+8654A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76090 | ||||||
| chr12:76131
|
C | CA | 8 | a0001c0002t0002g0039a0001c0003t0001g0044a0001c0007t0001g0042others(5): Show | 8 | HG02015.hp1 HG02074.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.554+8697dupA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 76131 | |||||
| chr12:76157
|
A | G | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8721A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76157 | ||||||
| chr12:76159
|
G | A | 8 | a0001c0004t0001g0091a0001c0041t0056g0072a0002c0015t0031g0207others(5): Show | 8 | HG01884.hp2 HG01952.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+8723G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76159 | ||||||
| chr12:76167
|
G | T | 1 | a0001c0004t0001g0053 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.554+8731G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76167 | ||||||
| chr12:76209
|
G | A | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8773G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76209 | ||||||
| chr12:76246
|
C | A | 2 | a0002c0001t0008g0052a0002c0001t0050g0051 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.554+8810C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76246 | ||||||
| chr12:76303
|
G | A | 1 | a0012c0023t0018g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.554+8867G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76303 | ||||||
| chr12:76311
|
G | A | 1 | a0007c0049t0002g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.554+8875G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76311 | ||||||
| chr12:76335
|
C | G | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8899C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76335 | ||||||
| chr12:76335
|
C | T | 2 | a0001c0024t0001g0032a0003c0005t0003g0033 | 2 | HG01123.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.554+8899C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76335 | ||||||
| chr12:76386
|
G | A | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+8950G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76386 | ||||||
| chr12:76538
|
A | G | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+9102A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76538 | ||||||
| chr12:76548
|
C | G | 1 | a0003c0005t0003g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.554+9112C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76548 | ||||||
| chr12:76622
|
G | T | 9 | a0001c0003t0002g0060a0001c0004t0001g0053a0002c0001t0005g0054others(6): Show | 9 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.554+9186G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76622 | ||||||
| chr12:76626
|
A | G | 2 | a0012c0023t0018g0276a0018c0054t0014g0279 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.554+9190A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76626 | ||||||
| chr12:76780
|
C | T | 1 | a0007c0021t0004g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.554+9344C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76780 | ||||||
| chr12:76789
|
C | G | 1 | a0012c0023t0018g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.554+9353C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76789 | ||||||
| chr12:76807
|
T | C | 1 | a0012c0023t0018g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.554+9371T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76807 | ||||||
| chr12:76811
|
G | A | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.554+9375G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76811 | ||||||
| chr12:76815
|
T | G | 1 | a0012c0023t0018g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.554+9379T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76815 | ||||||
| chr12:76841
|
G | C | 2 | a0001c0024t0001g0032a0003c0005t0003g0033 | 2 | HG01123.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.554+9405G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76841 | ||||||
| chr12:76983
|
G | T | 1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.554+9547G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76983 | ||||||
| chr12:76986
|
T | C | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+9550T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 76986 | ||||||
| chr12:77037
|
T | G | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+9601T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77037 | ||||||
| chr12:77065
|
T | C | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+9629T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77065 | ||||||
| chr12:77241
|
G | A | 4 | a0001c0002t0002g0035a0002c0001t0022g0038a0003c0005t0009g0077others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+9805G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77241 | ||||||
| chr12:77315
|
G | A | 1 | a0002c0001t0022g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.554+9879G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77315 | ||||||
| chr12:77457
|
C | G | 2 | a0001c0024t0001g0032a0003c0005t0003g0033 | 2 | HG01123.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.554+10021C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77457 | ||||||
| chr12:77606
|
G | A | 40 | a0001c0002t0002g0001a0001c0002t0002g0218a0001c0002t0002g0239others(37): Show | 41 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.554+10170G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77606 | ||||||
| chr12:77674
|
T | G | 10 | a0001c0002t0002g0039a0001c0003t0001g0044a0001c0003t0001g0045others(7): Show | 10 | HG01993.hp1 HG02015.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+10238T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77674 | ||||||
| chr12:77768
|
C | T | 9 | a0001c0002t0002g0039a0001c0003t0001g0044a0001c0003t0001g0045others(6): Show | 9 | HG01993.hp1 HG02015.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+10332C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77768 | ||||||
| chr12:77861
|
A | C | 97 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0239others(94): Show | 98 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.554+10425A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77861 | ||||||
| chr12:77900
|
G | A | 5 | a0001c0002t0002g0066a0001c0004t0002g0070a0002c0001t0008g0067others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+10464G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77900 | ||||||
| chr12:77915
|
C | T | 3 | a0001c0006t0002g0145a0001c0006t0049g0144a0016c0057t0014g0274 | 3 | HG00642.hp2 HG00733.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.554+10479C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77915 | ||||||
| chr12:77954
|
C | G | 3 | a0001c0006t0002g0145a0001c0006t0049g0144a0016c0057t0014g0274 | 3 | HG00642.hp2 HG00733.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.554+10518C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 77954 | ||||||
| chr12:78026
|
C | T | 3 | a0001c0003t0005g0193a0001c0041t0056g0072a0002c0001t0009g0192 | 3 | HG01891.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.554+10590C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78026 | ||||||
| chr12:78043
|
C | T | 1 | a0001c0024t0001g0032 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.554+10607C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78043 | ||||||
| chr12:78044
|
G | C | 266 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.554+10608G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78044 | ||||||
| chr12:78054
|
G | A | 1 | a0002c0001t0020g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.554+10618G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78054 | ||||||
| chr12:78055
|
C | T | 1 | a0001c0042t0001g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.554+10619C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78055 | ||||||
| chr12:78138
|
C | CCCGCGCG others(41): Show |
1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.554+10708_554+1070 others(52): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 78138 | |||||
| chr12:78200
|
C | G | 1 | a0001c0002t0002g0137 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.554+10764C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78200 | ||||||
| chr12:78224
|
G | C | 15 | a0001c0002t0002g0066a0001c0003t0002g0060a0001c0004t0001g0053others(12): Show | 15 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.554+10788G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78224 | ||||||
| chr12:78236
|
G | C | 1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.554+10800G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78236 | ||||||
| chr12:78244
|
G | C | 1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.554+10808G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78244 | ||||||
| chr12:78247
|
A | T | 1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.554+10811A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78247 | ||||||
| chr12:78250
|
G | T | 1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.554+10814G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78250 | ||||||
| chr12:78251
|
C | G | 1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.554+10815C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78251 | ||||||
| chr12:78294
|
C | A | 1 | a0002c0001t0020g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.554+10858C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78294 | ||||||
| chr12:78294
|
C | CGGGTGCT others(7): Show |
3 | a0001c0043t0004g0063a0002c0001t0024g0017a0014c0028t0001g0062 | 3 | HG01167.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.554+10865_554+1087 others(18): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 78294 | |||||
| chr12:78375
|
G | C | 137 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.554+10939G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78375 | ||||||
| chr12:78435
|
G | A | 1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.554+10999G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78435 | ||||||
| chr12:78499
|
C | A | 2 | a0001c0003t0012g0049a0024c0036t0057g0048 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.554+11063C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78499 | ||||||
| chr12:78505
|
C | CA | 92 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0218others(89): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.554+11081dupA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 78505 | |||||
| chr12:78505
|
C | CAA | 28 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0007g0003others(25): Show | 28 | HG01074.hp1 HG01346.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.554+11080_554+1108 others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 78505 | |||||
| chr12:78505
|
CAA | C | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+11080_554+1108 others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 78505 | |||||
| chr12:78514
|
A | AT | 8 | a0001c0002t0002g0035a0001c0003t0012g0049a0002c0001t0022g0038others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+11078_554+1107 others(5): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78514 | ||||||
| chr12:78552
|
T | C | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+11116T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78552 | ||||||
| chr12:78562
|
G | A | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+11126G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78562 | ||||||
| chr12:78735
|
G | A | 3 | a0002c0001t0024g0177a0003c0010t0019g0178a0004c0011t0004g0146 | 3 | HG02630.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.554+11299G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78735 | ||||||
| chr12:78922
|
C | T | 1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.554+11486C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 78922 | ||||||
| chr12:79031
|
C | G | 35 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0003t0001g0267others(32): Show | 35 | HG01074.hp1 HG01167.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.554+11595C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79031 | ||||||
| chr12:79038
|
A | G | 3 | a0001c0044t0001g0050a0002c0001t0008g0052a0002c0001t0050g0051 | 3 | HG02965.hp1 HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.554+11602A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79038 | ||||||
| chr12:79119
|
C | T | 133 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(130): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.554+11683C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79119 | ||||||
| chr12:79169
|
T | A | 6 | a0001c0002t0047g0201a0001c0003t0001g0204a0001c0006t0002g0188others(3): Show | 6 | HG01168.hp2 HG01257.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+11733T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79169 | ||||||
| chr12:79169
|
T | G | 2 | a0001c0043t0004g0063a0014c0028t0001g0062 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.554+11733T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79169 | ||||||
| chr12:79182
|
G | T | 10 | a0001c0002t0002g0039a0001c0003t0001g0044a0001c0003t0001g0045others(7): Show | 10 | HG01993.hp1 HG02015.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+11746G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79182 | ||||||
| chr12:79230
|
A | AC | 133 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(130): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.554+11800dupC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 79230 | |||||
| chr12:79234
|
C | T | 2 | a0001c0003t0005g0193a0002c0001t0009g0192 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.554+11798C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79234 | ||||||
| chr12:79470
|
A | G | 9 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0007t0001g0042others(6): Show | 9 | HG01993.hp1 HG02015.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+12034A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79470 | ||||||
| chr12:79516
|
G | A | 1 | a0001c0002t0002g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.554+12080G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79516 | ||||||
| chr12:79525
|
C | T | 8 | a0001c0002t0002g0035a0001c0003t0012g0049a0002c0001t0022g0038others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+12089C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79525 | ||||||
| chr12:79691
|
A | G | 1 | a0001c0006t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.554+12255A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79691 | ||||||
| chr12:79810
|
C | T | 9 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0007t0001g0042others(6): Show | 9 | HG01993.hp1 HG02015.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+12374C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79810 | ||||||
| chr12:79851
|
C | G | 8 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(5): Show | 8 | HG01074.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.554+12415C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79851 | ||||||
| chr12:79927
|
G | C | 70 | a0001c0002t0002g0001a0001c0002t0002g0218a0001c0002t0002g0239others(67): Show | 71 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.554+12491G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 79927 | ||||||
| chr12:80003
|
C | T | 7 | a0003c0005t0002g0252a0003c0005t0023g0245a0003c0010t0007g0268others(4): Show | 7 | HG01167.hp2 HG01346.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.554+12567C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80003 | ||||||
| chr12:80098
|
T | G | 2 | a0001c0003t0012g0049a0024c0036t0057g0048 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.554+12662T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80098 | ||||||
| chr12:80287
|
G | A | 2 | a0003c0005t0012g0074a0003c0005t0062g0073 | 2 | HG01952.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.554+12851G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80287 | ||||||
| chr12:80298
|
T | G | 11 | a0001c0002t0002g0066a0001c0004t0002g0070a0001c0004t0004g0031others(8): Show | 11 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.554+12862T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80298 | ||||||
| chr12:80306
|
G | A | 8 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(5): Show | 8 | HG01074.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.554+12870G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80306 | ||||||
| chr12:80360
|
G | A | 2 | a0002c0001t0009g0064a0006c0012t0004g0065 | 2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+12924G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80360 | ||||||
| chr12:80503
|
G | A | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+13067G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80503 | ||||||
| chr12:80653
|
C | CA | 13 | a0001c0003t0002g0060a0001c0004t0001g0053a0001c0044t0001g0050others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.554+13224dupA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 80653 | |||||
| chr12:80699
|
T | C | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.554+13263T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80699 | ||||||
| chr12:80870
|
C | T | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.554+13434C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80870 | ||||||
| chr12:80881
|
G | A | 25 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0003t0007g0003others(22): Show | 25 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.554+13445G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80881 | ||||||
| chr12:80886
|
G | A | 34 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0003t0001g0044others(31): Show | 34 | HG01884.hp1 HG01993.hp1 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.554+13450G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80886 | ||||||
| chr12:80931
|
G | A | 3 | a0001c0024t0001g0032a0003c0005t0003g0033a0004c0008t0052g0247 | 3 | HG01123.hp2 HG04228.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.554+13495G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80931 | ||||||
| chr12:80936
|
A | C | 3 | a0001c0024t0001g0032a0003c0005t0003g0033a0004c0008t0052g0247 | 3 | HG01123.hp2 HG04228.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.554+13500A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80936 | ||||||
| chr12:80964
|
G | C | 1 | a0001c0042t0001g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.554+13528G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 80964 | ||||||
| chr12:81024
|
C | A | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.554+13588C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 81024 | ||||||
| chr12:81128
|
C | T | 1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.554+13692C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 81128 | ||||||
| chr12:81241
|
CCT | C | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+13806_554+1380 others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 81241 | ||||||
| chr12:81551
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.554+14115G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 81551 | ||||||
| chr12:81741
|
G | A | 1 | a0001c0004t0001g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.554+14305G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 81741 | ||||||
| chr12:81814
|
A | G | 13 | a0001c0003t0002g0169a0001c0004t0001g0170a0001c0037t0011g0194others(10): Show | 13 | HG00597.hp2 HG00621.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.554+14378A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 81814 | ||||||
| chr12:82130
|
T | A | 2 | a0008c0016t0007g0058a0014c0029t0054g0059 | 2 | HG01081.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.554+14694T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82130 | ||||||
| chr12:82152
|
C | T | 3 | a0003c0005t0019g0226a0003c0005t0028g0228a0005c0018t0008g0227 | 3 | HG02486.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.554+14716C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82152 | ||||||
| chr12:82284
|
T | C | 64 | a0001c0002t0002g0001a0001c0002t0002g0218a0001c0002t0002g0239others(61): Show | 65 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.554+14848T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82284 | ||||||
| chr12:82359
|
G | A | 12 | a0001c0002t0002g0096a0001c0002t0002g0098a0001c0002t0044g0084others(9): Show | 12 | HG00741.hp2 HG01168.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.554+14923G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82359 | ||||||
| chr12:82453
|
G | A | 106 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(103): Show | 107 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.554+15017G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82453 | ||||||
| chr12:82646
|
G | A | 10 | a0001c0003t0002g0060a0001c0004t0001g0053a0002c0001t0005g0054others(7): Show | 10 | HG00735.hp1 HG01081.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.554+15210G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82646 | ||||||
| chr12:82726
|
C | T | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.554+15290C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82726 | ||||||
| chr12:82727
|
G | A | 2 | a0001c0002t0002g0099a0001c0002t0002g0100 | 2 | NA18962.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.554+15291G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82727 | ||||||
| chr12:82947
|
G | T | 2 | a0002c0001t0008g0052a0002c0001t0050g0051 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.554+15511G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82947 | ||||||
| chr12:82957
|
A | T | 2 | a0002c0001t0008g0052a0002c0001t0050g0051 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.554+15521A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 82957 | ||||||
| chr12:83054
|
G | A | 105 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(102): Show | 106 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.554+15618G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83054 | ||||||
| chr12:83100
|
G | C | 33 | a0001c0002t0002g0066a0001c0003t0002g0060a0001c0004t0001g0053others(30): Show | 33 | HG00735.hp1 HG01081.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.554+15664G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83100 | ||||||
| chr12:83178
|
A | G | 1 | a0008c0035t0007g0135 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.554+15742A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83178 | ||||||
| chr12:83295
|
C | T | 1 | a0001c0003t0001g0044 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.555-15851C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83295 | ||||||
| chr12:83444
|
C | T | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.555-15702C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83444 | ||||||
| chr12:83614
|
G | A | 1 | a0006c0012t0032g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.555-15532G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83614 | ||||||
| chr12:83677
|
G | A | 108 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(105): Show | 109 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.555-15469G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83677 | ||||||
| chr12:83702
|
C | T | 105 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(102): Show | 106 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.555-15444C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83702 | ||||||
| chr12:83711
|
A | G | 119 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(116): Show | 120 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.555-15435A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83711 | ||||||
| chr12:83824
|
T | C | 117 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(114): Show | 118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.555-15322T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 83824 | ||||||
| chr12:84145
|
G | A | 7 | a0001c0002t0002g0090a0001c0002t0002g0182a0001c0003t0001g0101others(4): Show | 7 | HG00099.hp1 HG00642.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.555-15001G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84145 | ||||||
| chr12:84151
|
T | C | 6 | a0001c0002t0002g0035a0002c0001t0022g0038a0003c0005t0009g0077others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-14995T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84151 | ||||||
| chr12:84382
|
G | T | 6 | a0002c0001t0005g0054a0003c0005t0009g0055a0003c0005t0059g0061others(3): Show | 6 | HG00735.hp1 HG01167.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.555-14764G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84382 | ||||||
| chr12:84441
|
C | T | 1 | a0001c0002t0002g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.555-14705C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84441 | ||||||
| chr12:84476
|
A | T | 15 | a0001c0002t0002g0008a0001c0003t0007g0003a0001c0003t0007g0004others(12): Show | 15 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.555-14670A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84476 | ||||||
| chr12:84481
|
T | C | 5 | a0002c0001t0005g0054a0003c0005t0009g0055a0003c0005t0059g0061others(2): Show | 5 | HG00735.hp1 HG01167.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-14665T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84481 | ||||||
| chr12:84542
|
C | T | 1 | a0001c0003t0001g0101 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.555-14604C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84542 | ||||||
| chr12:84652
|
C | T | 71 | a0001c0002t0002g0035a0001c0002t0002g0218a0001c0002t0002g0239others(68): Show | 71 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.555-14494C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84652 | ||||||
| chr12:84754
|
T | C | 32 | a0001c0002t0002g0096a0001c0002t0002g0098a0001c0002t0044g0084others(29): Show | 32 | HG00621.hp2 HG00735.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.555-14392T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84754 | ||||||
| chr12:84857
|
A | G | 3 | a0001c0003t0001g0225a0001c0003t0012g0049a0024c0036t0057g0048 | 3 | HG02055.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.555-14289A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 84857 | ||||||
| chr12:85028
|
A | C | 1 | a0014c0029t0054g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.555-14118A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85028 | ||||||
| chr12:85163
|
G | A | 1 | a0003c0045t0045g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.555-13983G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85163 | ||||||
| chr12:85166
|
A | G | 12 | a0001c0002t0002g0008a0001c0002t0002g0066a0001c0004t0002g0070others(9): Show | 12 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.555-13980A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85166 | ||||||
| chr12:85173
|
G | A | 5 | a0001c0041t0056g0072a0002c0015t0031g0207a0003c0005t0012g0074others(2): Show | 5 | HG01884.hp2 HG01952.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-13973G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85173 | ||||||
| chr12:85185
|
G | A | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0003g0041others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-13961G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85185 | ||||||
| chr12:85200
|
G | A | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555-13946G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85200 | ||||||
| chr12:85224
|
GA | G | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.555-13921delA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85224 | ||||||
| chr12:85401
|
G | A | 1 | a0001c0041t0056g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.555-13745G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85401 | ||||||
| chr12:85421
|
G | A | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555-13725G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85421 | ||||||
| chr12:85457
|
G | T | 1 | a0002c0001t0016g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.555-13689G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85457 | ||||||
| chr12:85520
|
T | G | 3 | a0001c0041t0056g0072a0003c0005t0012g0074a0003c0005t0062g0073 | 3 | HG01952.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.555-13626T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85520 | ||||||
| chr12:85663
|
G | A | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.555-13483G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85663 | ||||||
| chr12:85685
|
G | A | 13 | a0001c0002t0002g0008a0001c0003t0007g0003a0001c0003t0007g0004others(10): Show | 13 | HG02145.hp1 HG02280.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.555-13461G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85685 | ||||||
| chr12:85711
|
C | A | 5 | a0001c0002t0002g0066a0001c0004t0002g0070a0002c0001t0008g0067others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-13435C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85711 | ||||||
| chr12:85824
|
C | T | 13 | a0001c0003t0005g0193a0001c0004t0004g0031a0001c0004t0035g0030others(10): Show | 13 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.555-13322C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85824 | ||||||
| chr12:85900
|
A | G | 2 | a0002c0001t0016g0241a0004c0011t0003g0046 | 2 | HG01243.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.555-13246A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 85900 | ||||||
| chr12:86143
|
A | G | 130 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(127): Show | 131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.555-13003A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86143 | ||||||
| chr12:86169
|
T | C | 130 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(127): Show | 131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.555-12977T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86169 | ||||||
| chr12:86182
|
G | A | 1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.555-12964G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86182 | ||||||
| chr12:86525
|
A | T | 1 | a0002c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.555-12621A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86525 | ||||||
| chr12:86532
|
C | A | 1 | a0002c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.555-12614C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86532 | ||||||
| chr12:86546
|
C | A | 1 | a0002c0009t0002g0080 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.555-12600C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86546 | ||||||
| chr12:86687
|
T | G | 2 | a0001c0002t0044g0084a0001c0007t0001g0042 | 2 | HG02027.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.555-12459T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86687 | ||||||
| chr12:86748
|
T | G | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-12398T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86748 | ||||||
| chr12:86952
|
T | C | 1 | a0001c0019t0034g0244 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.555-12194T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 86952 | ||||||
| chr12:87067
|
G | A | 1 | a0001c0019t0034g0244 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.555-12079G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87067 | ||||||
| chr12:87177
|
A | G | 2 | a0001c0002t0002g0133a0001c0002t0002g0137 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.555-11969A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87177 | ||||||
| chr12:87224
|
G | A | 5 | a0001c0002t0002g0066a0001c0004t0002g0070a0002c0001t0008g0067others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-11922G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87224 | ||||||
| chr12:87265
|
C | T | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-11881C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87265 | ||||||
| chr12:87302
|
T | C | 1 | a0001c0059t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.555-11844T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87302 | ||||||
| chr12:87324
|
A | G | 3 | a0001c0044t0001g0050a0002c0001t0050g0051a0005c0031t0001g0057 | 3 | HG02280.hp1 HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.555-11822A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87324 | ||||||
| chr12:87345
|
G | C | 1 | a0001c0007t0001g0107 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.555-11801G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87345 | ||||||
| chr12:87409
|
G | C | 57 | a0001c0002t0002g0001a0001c0002t0002g0218a0001c0002t0002g0239others(54): Show | 58 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.555-11737G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87409 | ||||||
| chr12:87417
|
G | A | 2 | a0007c0021t0004g0253a0016c0057t0014g0274 | 2 | HG00733.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.555-11729G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87417 | ||||||
| chr12:87444
|
G | A | 132 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(129): Show | 133 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.555-11702G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87444 | ||||||
| chr12:87476
|
A | G | 1 | a0001c0004t0060g0217 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.555-11670A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87476 | ||||||
| chr12:87585
|
A | G | 2 | a0001c0002t0002g0240a0011c0055t0018g0271 | 2 | HG01175.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.555-11561A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87585 | ||||||
| chr12:87593
|
T | C | 1 | a0021c0032t0001g0108 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.555-11553T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87593 | ||||||
| chr12:87631
|
G | C | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555-11515G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87631 | ||||||
| chr12:87739
|
G | A | 1 | a0008c0035t0007g0135 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.555-11407G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87739 | ||||||
| chr12:87931
|
C | A | 6 | a0001c0002t0002g0035a0002c0001t0022g0038a0003c0005t0009g0077others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-11215C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87931 | ||||||
| chr12:87963
|
T | C | 1 | a0002c0009t0002g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.555-11183T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87963 | ||||||
| chr12:87968
|
C | A | 1 | a0002c0009t0002g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.555-11178C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87968 | ||||||
| chr12:87978
|
C | A | 1 | a0001c0002t0002g0167 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.555-11168C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 87978 | ||||||
| chr12:88174
|
T | A | 2 | a0002c0001t0009g0064a0006c0012t0004g0065 | 2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.555-10972T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 88174 | ||||||
| chr12:88243
|
C | T | 1 | a0001c0024t0001g0032 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.555-10903C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 88243 | ||||||
| chr12:88556
|
A | G | 1 | a0005c0018t0001g0248 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.555-10590A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 88556 | ||||||
| chr12:88581
|
C | A | 1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.555-10565C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 88581 | ||||||
| chr12:88675
|
C | T | 130 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(127): Show | 131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.555-10471C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 88675 | ||||||
| chr12:88699
|
C | A | 1 | a0001c0003t0001g0088 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.555-10447C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 88699 | ||||||
| chr12:88793
|
A | G | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-10353A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 88793 | ||||||
| chr12:89098
|
C | T | 1 | a0001c0004t0003g0082 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.555-10048C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89098 | ||||||
| chr12:89311
|
T | TG | 14 | a0001c0002t0002g0008a0001c0003t0007g0003a0001c0003t0007g0004others(11): Show | 14 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.555-9833dupG | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 89311 | |||||
| chr12:89331
|
G | A | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-9815G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89331 | ||||||
| chr12:89343
|
G | A | 2 | a0001c0002t0002g0182a0001c0019t0034g0244 | 2 | HG00099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.555-9803G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89343 | ||||||
| chr12:89401
|
A | G | 1 | a0001c0024t0001g0032 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.555-9745A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89401 | ||||||
| chr12:89547
|
A | G | 1 | a0001c0003t0001g0088 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.555-9599A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89547 | ||||||
| chr12:89606
|
T | C | 6 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(3): Show | 6 | HG01993.hp1 HG02135.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-9540T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89606 | ||||||
| chr12:89640
|
C | CTCTT | 133 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(130): Show | 134 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.555-9503_555-9502i others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 89640 | |||||
| chr12:89683
|
G | A | 6 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(3): Show | 6 | HG01993.hp1 HG02135.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-9463G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89683 | ||||||
| chr12:89684
|
G | A | 6 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(3): Show | 6 | HG01993.hp1 HG02135.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-9462G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89684 | ||||||
| chr12:89760
|
C | T | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-9386C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89760 | ||||||
| chr12:89825
|
A | C | 7 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(4): Show | 7 | HG01081.hp2 HG01993.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.555-9321A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89825 | ||||||
| chr12:89883
|
A | G | 1 | a0002c0009t0002g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.555-9263A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89883 | ||||||
| chr12:89924
|
G | A | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-9222G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 89924 | ||||||
| chr12:90063
|
G | A | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-9083G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90063 | ||||||
| chr12:90081
|
G | A | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.555-9065G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90081 | ||||||
| chr12:90187
|
C | T | 1 | a0011c0058t0027g0272 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.555-8959C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90187 | ||||||
| chr12:90328
|
A | T | 104 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0066others(101): Show | 105 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.555-8818A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90328 | ||||||
| chr12:90365
|
G | A | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-8781G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90365 | ||||||
| chr12:90366
|
T | C | 134 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(131): Show | 135 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.555-8780T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90366 | ||||||
| chr12:90367
|
G | A | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0003g0041others(1): Show | 4 | HG01993.hp1 HG02135.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-8779G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90367 | ||||||
| chr12:90385
|
C | T | 3 | a0001c0024t0001g0032a0002c0001t0008g0052a0003c0005t0003g0033 | 3 | HG01123.hp2 HG02965.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.555-8761C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90385 | ||||||
| chr12:90580
|
T | C | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.555-8566T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90580 | ||||||
| chr12:90600
|
G | GA | 134 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(131): Show | 135 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.555-8546_555-8545i others(3): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90600 | ||||||
| chr12:90614
|
A | T | 1 | a0002c0001t0020g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.555-8532A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90614 | ||||||
| chr12:90935
|
T | C | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.555-8211T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 90935 | ||||||
| chr12:91058
|
C | A | 8 | a0001c0003t0002g0060a0001c0004t0001g0053a0001c0006t0002g0106others(5): Show | 8 | HG00621.hp2 HG00735.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-8088C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91058 | ||||||
| chr12:91080
|
G | T | 2 | a0001c0003t0005g0193a0002c0001t0009g0192 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.555-8066G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91080 | ||||||
| chr12:91085
|
G | A | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555-8061G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91085 | ||||||
| chr12:91156
|
C | T | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-7990C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91156 | ||||||
| chr12:91265
|
C | G | 1 | a0001c0002t0003g0174 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.555-7881C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91265 | ||||||
| chr12:91301
|
C | G | 3 | a0001c0004t0003g0082a0002c0009t0002g0080a0002c0009t0002g0081 | 3 | HG01517.hp1 HG02273.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.555-7845C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91301 | ||||||
| chr12:91333
|
C | T | 4 | a0002c0001t0009g0064a0006c0012t0004g0065a0008c0016t0007g0058others(1): Show | 4 | HG01081.hp2 HG02897.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-7813C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91333 | ||||||
| chr12:91454
|
G | A | 1 | a0011c0058t0027g0272 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.555-7692G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91454 | ||||||
| chr12:91502
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0218others(83): Show | 87 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.555-7644C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91502 | ||||||
| chr12:91528
|
A | G | 6 | a0001c0003t0005g0193a0001c0041t0056g0072a0002c0001t0009g0192others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.555-7618A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91528 | ||||||
| chr12:91674
|
G | A | 2 | a0002c0001t0050g0051a0005c0031t0001g0057 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.555-7472G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91674 | ||||||
| chr12:91687
|
G | A | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-7459G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91687 | ||||||
| chr12:91735
|
C | T | 1 | a0004c0011t0006g0132 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.555-7411C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91735 | ||||||
| chr12:91768
|
G | A | 1 | a0002c0001t0006g0097 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.555-7378G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91768 | ||||||
| chr12:91790
|
A | T | 1 | a0004c0011t0004g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.555-7356A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91790 | ||||||
| chr12:91793
|
G | A | 1 | a0003c0010t0015g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.555-7353G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91793 | ||||||
| chr12:91812
|
G | A | 13 | a0001c0002t0002g0008a0001c0003t0007g0003a0001c0003t0007g0004others(10): Show | 13 | HG02145.hp1 HG02280.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.555-7334G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91812 | ||||||
| chr12:91814
|
G | A | 13 | a0001c0003t0005g0193a0001c0004t0004g0031a0001c0004t0035g0030others(10): Show | 13 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.555-7332G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91814 | ||||||
| chr12:91995
|
T | C | 1 | a0002c0001t0041g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.555-7151T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 91995 | ||||||
| chr12:92053
|
A | G | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-7093A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92053 | ||||||
| chr12:92070
|
C | A | 1 | a0002c0001t0003g0140 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.555-7076C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92070 | ||||||
| chr12:92076
|
G | A | 104 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0066others(101): Show | 105 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.555-7070G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92076 | ||||||
| chr12:92152
|
T | G | 1 | a0023c0039t0030g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.555-6994T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92152 | ||||||
| chr12:92192
|
C | T | 2 | a0001c0006t0010g0209a0001c0006t0010g0210 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.555-6954C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92192 | ||||||
| chr12:92295
|
G | A | 1 | a0001c0004t0001g0109 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.555-6851G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92295 | ||||||
| chr12:92355
|
G | A | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-6791G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92355 | ||||||
| chr12:92364
|
G | A | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555-6782G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92364 | ||||||
| chr12:92429
|
T | TGTCAC | 7 | a0001c0003t0002g0060a0001c0004t0001g0053a0001c0006t0002g0106others(4): Show | 7 | HG00621.hp2 HG00735.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.555-6716_555-6712d others(7): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 92429 | |||||
| chr12:92431
|
T | C | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-6715T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92431 | ||||||
| chr12:92481
|
T | C | 2 | a0003c0005t0012g0074a0003c0005t0062g0073 | 2 | HG01952.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.555-6665T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92481 | ||||||
| chr12:92632
|
C | T | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(2): Show | 5 | HG01993.hp1 HG02135.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-6514C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92632 | ||||||
| chr12:92702
|
G | C | 132 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(129): Show | 133 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.555-6444G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92702 | ||||||
| chr12:92738
|
C | T | 5 | a0001c0002t0002g0066a0001c0004t0002g0070a0002c0001t0008g0067others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-6408C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92738 | ||||||
| chr12:92928
|
T | C | 14 | a0001c0002t0002g0240a0001c0002t0002g0261a0001c0002t0055g0256others(11): Show | 14 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.555-6218T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92928 | ||||||
| chr12:92966
|
T | G | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.555-6180T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92966 | ||||||
| chr12:92974
|
G | A | 2 | a0001c0006t0010g0209a0001c0006t0010g0210 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.555-6172G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 92974 | ||||||
| chr12:93115
|
G | C | 1 | a0002c0001t0020g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.555-6031G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93115 | ||||||
| chr12:93452
|
G | C | 2 | a0003c0005t0012g0074a0003c0005t0062g0073 | 2 | HG01952.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.555-5694G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93452 | ||||||
| chr12:93492
|
G | A | 3 | a0001c0004t0003g0082a0002c0009t0002g0080a0002c0009t0002g0081 | 3 | HG01517.hp1 HG02273.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.555-5654G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93492 | ||||||
| chr12:93614
|
A | G | 1 | a0002c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.555-5532A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93614 | ||||||
| chr12:93672
|
T | C | 130 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(127): Show | 131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.555-5474T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93672 | ||||||
| chr12:93711
|
C | T | 130 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(127): Show | 131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.555-5435C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93711 | ||||||
| chr12:93763
|
G | T | 2 | a0001c0002t0002g0133a0001c0002t0002g0137 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.555-5383G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93763 | ||||||
| chr12:93773
|
T | C | 1 | a0002c0001t0001g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.555-5373T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93773 | ||||||
| chr12:93817
|
G | A | 4 | a0002c0001t0009g0064a0006c0012t0004g0065a0008c0016t0007g0058others(1): Show | 4 | HG01081.hp2 HG02897.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-5329G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93817 | ||||||
| chr12:93944
|
G | A | 1 | a0025c0027t0038g0040 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.555-5202G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 93944 | ||||||
| chr12:94135
|
T | G | 1 | a0002c0001t0036g0161 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.555-5011T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94135 | ||||||
| chr12:94173
|
C | G | 2 | a0002c0001t0001g0184a0002c0001t0003g0183 | 2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.555-4973C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94173 | ||||||
| chr12:94276
|
T | G | 1 | a0001c0033t0013g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.555-4870T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94276 | ||||||
| chr12:94474
|
G | C | 99 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0066others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.555-4672G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94474 | ||||||
| chr12:94526
|
G | A | 11 | a0001c0002t0002g0035a0001c0003t0012g0049a0001c0024t0001g0032others(8): Show | 11 | HG01123.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.555-4620G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94526 | ||||||
| chr12:94580
|
G | A | 2 | a0001c0002t0003g0174a0001c0025t0040g0148 | 2 | HG00673.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.555-4566G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94580 | ||||||
| chr12:94629
|
G | A | 6 | a0001c0003t0001g0111a0001c0003t0001g0141a0001c0003t0004g0166others(3): Show | 6 | HG01496.hp2 HG01934.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-4517G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94629 | ||||||
| chr12:94637
|
G | A | 2 | a0002c0001t0024g0017a0002c0015t0031g0207 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.555-4509G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94637 | ||||||
| chr12:94685
|
C | A | 2 | a0001c0002t0002g0240a0011c0055t0018g0271 | 2 | HG01175.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.555-4461C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94685 | ||||||
| chr12:94971
|
CT | C | 12 | a0001c0003t0005g0193a0001c0004t0004g0031a0001c0004t0035g0030others(9): Show | 12 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.555-4174delT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 94971 | ||||||
| chr12:95039
|
G | A | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.555-4107G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 95039 | ||||||
| chr12:95191
|
G | A | 1 | a0004c0008t0003g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.555-3955G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 95191 | ||||||
| chr12:95320
|
T | G | 2 | a0001c0034t0001g0214a0002c0009t0002g0213 | 2 | HG00438.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.555-3826T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 95320 | ||||||
| chr12:95382
|
G | C | 1 | a0001c0004t0001g0109 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.555-3764G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 95382 | ||||||
| chr12:95512
|
G | T | 129 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(126): Show | 130 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.555-3634G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 95512 | ||||||
| chr12:95562
|
C | T | 17 | a0001c0003t0001g0045a0001c0003t0002g0219a0001c0003t0005g0193others(14): Show | 17 | HG01243.hp1 HG01358.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.555-3584C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 95562 | ||||||
| chr12:95889
|
T | C | 2 | a0002c0001t0050g0051a0005c0031t0001g0057 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.555-3257T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 95889 | ||||||
| chr12:95904
|
T | G | 1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.555-3242T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 95904 | ||||||
| chr12:96035
|
TC | T | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0003g0041others(1): Show | 4 | HG01993.hp1 HG02135.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-3109delC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 96035 | |||||
| chr12:96054
|
A | G | 1 | a0001c0006t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.555-3092A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96054 | ||||||
| chr12:96061
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0003g0041others(1): Show | 4 | HG01993.hp1 HG02135.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-3085T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96061 | ||||||
| chr12:96392
|
A | T | 1 | a0001c0003t0001g0204 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.555-2754A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96392 | ||||||
| chr12:96451
|
A | C | 1 | a0002c0009t0002g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.555-2695A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96451 | ||||||
| chr12:96695
|
T | C | 2 | a0003c0005t0013g0036a0008c0016t0007g0037 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.555-2451T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96695 | ||||||
| chr12:96733
|
G | A | 2 | a0001c0006t0010g0209a0001c0006t0010g0210 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.555-2413G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96733 | ||||||
| chr12:96896
|
G | A | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.555-2250G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96896 | ||||||
| chr12:96904
|
A | G | 1 | a0005c0031t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.555-2242A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96904 | ||||||
| chr12:96966
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0003g0041others(1): Show | 4 | HG01993.hp1 HG02135.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-2180T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 96966 | ||||||
| chr12:97079
|
A | G | 1 | a0001c0002t0003g0174 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.555-2067A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 97079 | ||||||
| chr12:97158
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.555-1988G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 97158 | ||||||
| chr12:97613
|
G | A | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.555-1533G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 97613 | ||||||
| chr12:97803
|
T | A | 128 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(125): Show | 129 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.555-1343T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 97803 | ||||||
| chr12:97815
|
G | A | 8 | a0001c0003t0001g0045a0001c0003t0002g0219a0001c0024t0001g0032others(5): Show | 8 | HG01123.hp2 HG01993.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.555-1331G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 97815 | ||||||
| chr12:97867
|
C | T | 8 | a0001c0003t0001g0045a0001c0003t0002g0219a0001c0024t0001g0032others(5): Show | 8 | HG01123.hp2 HG01993.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.555-1279C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 97867 | ||||||
| chr12:97932
|
C | T | 2 | a0002c0001t0024g0017a0002c0015t0031g0207 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.555-1214C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 97932 | ||||||
| chr12:98065
|
A | G | 37 | a0001c0002t0002g0127a0001c0002t0002g0167a0001c0002t0002g0205others(34): Show | 37 | HG00735.hp1 HG01123.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.555-1081A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98065 | ||||||
| chr12:98070
|
G | A | 1 | a0001c0002t0002g0001 | 2 | HG02027.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.555-1076G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98070 | ||||||
| chr12:98102
|
T | C | 1 | a0001c0003t0002g0102 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.555-1044T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98102 | ||||||
| chr12:98113
|
A | T | 1 | a0002c0040t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.555-1033A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98113 | ||||||
| chr12:98264
|
A | G | 5 | a0001c0004t0001g0053a0001c0043t0004g0063a0003c0005t0009g0055others(2): Show | 5 | HG00735.hp1 HG03579.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-882A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98264 | ||||||
| chr12:98417
|
C | T | 1 | a0002c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.555-729C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98417 | ||||||
| chr12:98445
|
T | C | 8 | a0001c0003t0001g0045a0001c0003t0002g0219a0001c0024t0001g0032others(5): Show | 8 | HG00673.hp1 HG01123.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-701T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98445 | ||||||
| chr12:98525
|
T | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0133others(82): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.555-621T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98525 | ||||||
| chr12:98605
|
C | T | 4 | a0001c0043t0004g0063a0003c0005t0009g0055a0003c0005t0059g0061others(1): Show | 4 | HG00735.hp1 HG03579.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-541C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98605 | ||||||
| chr12:98671
|
T | C | 5 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0003g0041others(2): Show | 5 | HG00673.hp1 HG01993.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-475T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98671 | ||||||
| chr12:98691
|
A | G | 129 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0066others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.555-455A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98691 | ||||||
| chr12:98720
|
C | T | 178 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0066others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.555-426C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98720 | ||||||
| chr12:98830
|
A | G | 3 | a0001c0002t0002g0125a0001c0003t0001g0044a0001c0003t0002g0187 | 3 | HG02015.hp1 HG02155.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.555-316A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98830 | ||||||
| chr12:98861
|
C | T | 1 | a0001c0004t0001g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.555-285C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 1/13 | chr12 | 98861 | ||||||
| chr12:99423
|
G | GCCCTGTC others(9): Show |
1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.623+212_623+227dup others(16): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 99423 | |||||
| chr12:99472
|
A | G | 2 | a0003c0010t0015g0263a0003c0010t0015g0266 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.623+258A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99472 | ||||||
| chr12:99527
|
C | G | 1 | a0001c0002t0002g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.623+313C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99527 | ||||||
| chr12:99541
|
G | A | 1 | a0002c0001t0003g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.623+327G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99541 | ||||||
| chr12:99618
|
T | C | 190 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(187): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.623+404T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99618 | ||||||
| chr12:99653
|
C | T | 167 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0090others(164): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.623+439C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99653 | ||||||
| chr12:99672
|
G | T | 185 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(182): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.623+458G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99672 | ||||||
| chr12:99728
|
G | C | 68 | a0001c0002t0002g0008a0001c0002t0002g0182a0001c0003t0001g0045others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.623+514G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99728 | ||||||
| chr12:99777
|
T | G | 188 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(185): Show | 189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.623+563T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99777 | ||||||
| chr12:99822
|
T | C | 1 | a0006c0012t0004g0065 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.623+608T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99822 | ||||||
| chr12:99834
|
G | A | 4 | a0001c0003t0039g0116a0001c0004t0003g0197a0001c0004t0003g0198others(1): Show | 4 | HG02056.hp1 HG02056.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.623+620G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99834 | ||||||
| chr12:99845
|
G | A | 1 | a0001c0006t0002g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.623+631G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99845 | ||||||
| chr12:99989
|
A | G | 2 | a0003c0005t0013g0036a0003c0005t0023g0245 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.623+775A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 99989 | ||||||
| chr12:100188
|
C | T | 60 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0218others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.623+974C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100188 | ||||||
| chr12:100189
|
C | T | 59 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0218others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.623+975C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100189 | ||||||
| chr12:100202
|
G | T | 29 | a0001c0002t0002g0167a0001c0003t0002g0060a0001c0004t0001g0053others(26): Show | 29 | HG01074.hp1 HG01255.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.623+988G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100202 | ||||||
| chr12:100278
|
G | A | 2 | a0002c0001t0024g0017a0002c0015t0031g0207 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.623+1064G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100278 | ||||||
| chr12:100312
|
A | T | 184 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(181): Show | 185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.623+1098A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100312 | ||||||
| chr12:100382
|
C | G | 24 | a0001c0002t0002g0167a0001c0003t0002g0060a0001c0004t0001g0053others(21): Show | 24 | HG01074.hp1 HG01255.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.623+1168C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100382 | ||||||
| chr12:100400
|
T | C | 126 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(123): Show | 127 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.623+1186T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100400 | ||||||
| chr12:100421
|
A | G | 3 | a0001c0003t0001g0225a0008c0016t0007g0037a0024c0036t0057g0048 | 3 | HG02622.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.623+1207A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100421 | ||||||
| chr12:100469
|
G | C | 1 | a0001c0006t0049g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.623+1255G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100469 | ||||||
| chr12:100480
|
C | T | 1 | a0005c0013t0025g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.623+1266C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100480 | ||||||
| chr12:100503
|
T | C | 184 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(181): Show | 185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.623+1289T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100503 | ||||||
| chr12:100595
|
C | T | 2 | a0002c0001t0050g0051a0005c0031t0001g0057 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.623+1381C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100595 | ||||||
| chr12:100660
|
C | T | 2 | a0002c0015t0013g0018a0008c0016t0007g0058 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.623+1446C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100660 | ||||||
| chr12:100772
|
A | G | 2 | a0003c0005t0002g0252a0005c0013t0001g0251 | 2 | HG01167.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.623+1558A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100772 | ||||||
| chr12:100901
|
T | G | 27 | a0001c0002t0002g0008a0001c0003t0001g0045a0001c0003t0002g0219others(24): Show | 27 | HG01106.hp1 HG01891.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.623+1687T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 100901 | ||||||
| chr12:101184
|
A | T | 274 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.623+1970A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101184 | ||||||
| chr12:101263
|
G | A | 1 | a0005c0013t0025g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.623+2049G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101263 | ||||||
| chr12:101271
|
C | T | 24 | a0001c0002t0002g0090a0001c0002t0002g0182a0001c0003t0001g0101others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.623+2057C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101271 | ||||||
| chr12:101272
|
G | A | 6 | a0004c0008t0001g0129a0004c0011t0006g0093a0004c0011t0006g0128others(3): Show | 6 | HG01981.hp2 NA18943.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+2058G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101272 | ||||||
| chr12:101337
|
G | A | 22 | a0001c0002t0002g0008a0001c0003t0005g0193a0001c0003t0007g0003others(19): Show | 22 | HG01106.hp1 HG01891.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.623+2123G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101337 | ||||||
| chr12:101343
|
A | G | 274 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.623+2129A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101343 | ||||||
| chr12:101397
|
C | T | 1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.623+2183C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101397 | ||||||
| chr12:101456
|
G | A | 1 | a0026c0026t0003g0165 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.623+2242G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101456 | ||||||
| chr12:101476
|
G | T | 59 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0218others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.623+2262G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101476 | ||||||
| chr12:101675
|
G | A | 1 | a0001c0042t0001g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.623+2461G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101675 | ||||||
| chr12:101745
|
C | T | 1 | a0004c0011t0003g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.623+2531C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101745 | ||||||
| chr12:101791
|
G | A | 25 | a0001c0002t0002g0167a0001c0003t0002g0060a0001c0004t0001g0053others(22): Show | 25 | HG01074.hp1 HG01167.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.623+2577G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101791 | ||||||
| chr12:101981
|
C | T | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.623+2767C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 101981 | ||||||
| chr12:102076
|
AGGCTCCT others(13): Show |
A | 1 | a0001c0041t0056g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.623+2895_623+2914d others(22): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 102076 | |||||
| chr12:102124
|
C | A | 2 | a0003c0005t0009g0281a0006c0012t0004g0065 | 2 | HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.623+2910C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102124 | ||||||
| chr12:102129
|
G | A | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.623+2915G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102129 | ||||||
| chr12:102187
|
C | T | 4 | a0002c0001t0024g0017a0002c0015t0013g0018a0002c0015t0031g0207others(1): Show | 4 | HG02109.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+2973C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102187 | ||||||
| chr12:102208
|
A | G | 5 | a0001c0002t0003g0174a0001c0003t0002g0169a0002c0001t0021g0163others(2): Show | 5 | HG00621.hp1 NA18941.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.623+2994A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102208 | ||||||
| chr12:102213
|
T | C | 1 | a0004c0011t0004g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.623+2999T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102213 | ||||||
| chr12:102405
|
C | T | 1 | a0003c0005t0012g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.623+3191C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102405 | ||||||
| chr12:102429
|
G | A | 1 | a0002c0001t0003g0183 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.623+3215G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102429 | ||||||
| chr12:102484
|
T | C | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.623+3270T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102484 | ||||||
| chr12:102486
|
A | G | 61 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0218others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.623+3272A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102486 | ||||||
| chr12:102487
|
C | G | 4 | a0001c0003t0001g0225a0002c0001t0020g0071a0008c0016t0007g0037others(1): Show | 4 | HG02622.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+3273C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102487 | ||||||
| chr12:102611
|
G | C | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+3397G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102611 | ||||||
| chr12:102755
|
C | A | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.623+3541C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102755 | ||||||
| chr12:102845
|
G | A | 4 | a0001c0002t0002g0099a0001c0002t0002g0100a0001c0002t0002g0112others(1): Show | 4 | NA18962.hp1 NA18963.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+3631G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 102845 | ||||||
| chr12:103000
|
C | T | 5 | a0001c0002t0002g0035a0001c0044t0001g0050a0003c0005t0009g0055others(2): Show | 5 | HG01884.hp1 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.623+3786C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103000 | ||||||
| chr12:103033
|
G | A | 62 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0090others(59): Show | 62 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.623+3819G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103033 | ||||||
| chr12:103132
|
G | A | 1 | a0001c0043t0004g0063 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.623+3918G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103132 | ||||||
| chr12:103140
|
T | G | 251 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.623+3926T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103140 | ||||||
| chr12:103189
|
C | T | 1 | a0001c0024t0001g0032 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.623+3975C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103189 | ||||||
| chr12:103193
|
C | A | 3 | a0001c0003t0001g0045a0001c0003t0002g0219a0011c0058t0027g0272 | 3 | HG01993.hp1 NA18942.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.623+3979C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103193 | ||||||
| chr12:103430
|
T | TGGCTCAG others(450): Show |
1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.623+4253_623+4254i others(459): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103430 | |||||
| chr12:103430
|
TGGCTCAG others(32): Show |
T | 1 | a0002c0001t0016g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.623+4241_623+4279d others(41): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103430 | |||||
| chr12:103462
|
A | AGAGGCAG others(349): Show |
2 | a0001c0006t0002g0145a0002c0001t0003g0216 | 2 | HG00323.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.623+4253_623+4254i others(358): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103462 | |||||
| chr12:103468
|
G | A | 277 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.623+4254G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103468 | ||||||
| chr12:103493
|
C | T | 1 | a0005c0018t0001g0248 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.623+4279C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103493 | ||||||
| chr12:103528
|
A | ACTCAGGA others(31): Show |
9 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(6): Show | 9 | HG01074.hp1 HG01358.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.623+4337_623+4338i others(40): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103528 | |||||
| chr12:103536
|
G | GGGAGAGG others(66): Show |
2 | a0002c0015t0013g0018a0008c0016t0007g0058 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.623+4339_623+4340i others(75): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103536 | |||||
| chr12:103552
|
G | A | 58 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0240others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.623+4338G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103552 | ||||||
| chr12:103563
|
A | G | 2 | a0002c0001t0050g0051a0005c0031t0001g0057 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.623+4349A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103563 | ||||||
| chr12:103574
|
G | A | 1 | a0005c0031t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.623+4360G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103574 | ||||||
| chr12:103575
|
G | T | 11 | a0001c0002t0002g0090a0001c0004t0011g0200a0001c0004t0012g0021others(8): Show | 11 | HG01074.hp1 HG01358.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.623+4361G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103575 | ||||||
| chr12:103578
|
G | A | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4364G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103578 | ||||||
| chr12:103579
|
T | G | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4365T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103579 | ||||||
| chr12:103580
|
G | GGAGTTCG others(30): Show |
1 | a0005c0031t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.623+4367_623+4368i others(39): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103580 | |||||
| chr12:103581
|
G | T | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4367G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103581 | ||||||
| chr12:103583
|
G | A | 1 | a0005c0031t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.623+4369G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103583 | ||||||
| chr12:103584
|
G | A | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4370G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103584 | ||||||
| chr12:103585
|
C | G | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4371C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103585 | ||||||
| chr12:103585
|
C | T | 1 | a0005c0031t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.623+4371C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103585 | ||||||
| chr12:103587
|
C | T | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4373C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103587 | ||||||
| chr12:103588
|
A | C | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4374A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103588 | ||||||
| chr12:103588
|
A | T | 1 | a0001c0003t0001g0101 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.623+4374A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103588 | ||||||
| chr12:103591
|
A | T | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4377A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103591 | ||||||
| chr12:103599
|
T | C | 4 | a0001c0002t0002g0090a0001c0004t0011g0200a0002c0001t0050g0051others(1): Show | 4 | HG02280.hp1 HG03139.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.623+4385T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103599 | ||||||
| chr12:103599
|
T | TGGGGCTC others(31): Show |
1 | a0009c0051t0001g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.623+4413_623+4450d others(40): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103599 | |||||
| chr12:103599
|
T | TGGGGCTC others(295): Show |
1 | a0001c0007t0001g0103 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.623+4412_623+4413i others(304): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103599 | |||||
| chr12:103600
|
G | A | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4386G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103600 | ||||||
| chr12:103600
|
G | GGGGCTCA others(182): Show |
2 | a0001c0006t0010g0209a0001c0006t0010g0210 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.623+4497_623+4498i others(191): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103600 | |||||
| chr12:103603
|
G | A | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+4389G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103603 | ||||||
| chr12:103603
|
G | GCTCAGGA others(181): Show |
3 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0022g0038 | 3 | HG01496.hp1 HG01516.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.623+4412_623+4413i others(190): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103603 | |||||
| chr12:103603
|
G | GCTCAGGA others(296): Show |
3 | a0002c0001t0004g0027a0002c0001t0004g0028a0002c0001t0004g0029 | 3 | HG01243.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.623+4412_623+4413i others(305): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103603 | |||||
| chr12:103627
|
A | G | 13 | a0001c0004t0011g0200a0001c0004t0012g0021a0001c0004t0012g0022others(10): Show | 13 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.623+4413A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103627 | ||||||
| chr12:103629
|
G | GGGGAGGC others(66): Show |
10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+4418_623+4419i others(75): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | GGGGGAGG others(182): Show |
1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.623+4423_623+4424i others(191): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | GGGGGAGG others(31): Show |
1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4424_623+4461d others(40): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | GGGGGAGG others(107): Show |
2 | a0001c0003t0010g0155a0002c0001t0001g0010 | 2 | HG00280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.623+4471_623+4472i others(116): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | GGGGGAGG others(294): Show |
2 | a0007c0021t0004g0253a0016c0057t0014g0274 | 2 | HG00733.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.623+4497_623+4498i others(303): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | GGGGGAGG others(220): Show |
6 | a0001c0004t0001g0180a0001c0006t0002g0196a0001c0019t0034g0244others(3): Show | 6 | HG01168.hp1 HG01255.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+4497_623+4498i others(229): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | GGGGGAGG others(975): Show |
1 | a0001c0006t0002g0092 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.623+4497_623+4498i others(984): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | GGGGGAGG others(451): Show |
1 | a0001c0004t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.623+4497_623+4498i others(460): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | GGGGGAGG others(292): Show |
1 | a0001c0002t0002g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.623+4580_623+4581i others(301): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103629 | |||||
| chr12:103629
|
G | T | 3 | a0001c0004t0011g0200a0001c0007t0001g0103a0005c0031t0001g0057 | 3 | HG02280.hp1 HG02717.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.623+4415G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103629 | ||||||
| chr12:103637
|
C | CAGGGCTC others(30): Show |
1 | a0001c0004t0011g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.623+4423_623+4424i others(39): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103637 | ||||||
| chr12:103637
|
C | CAGGGCTC others(30): Show |
1 | a0002c0009t0002g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.623+4423_623+4424i others(39): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103637 | ||||||
| chr12:103637
|
C | CGGGGCTC others(591): Show |
1 | a0001c0006t0002g0189 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.623+4497_623+4498i others(600): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103637 | |||||
| chr12:103638
|
G | A | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+4424G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103638 | ||||||
| chr12:103641
|
G | A | 12 | a0001c0004t0011g0200a0001c0004t0012g0021a0001c0004t0012g0022others(9): Show | 12 | HG00438.hp1 HG01074.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.623+4427G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103641 | ||||||
| chr12:103643
|
T | G | 6 | a0001c0025t0040g0148a0003c0010t0019g0178a0006c0012t0001g0265others(3): Show | 6 | HG00673.hp2 HG01081.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.623+4429T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103643 | ||||||
| chr12:103664
|
C | CA | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+4450_623+4451i others(3): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103664 | ||||||
| chr12:103667
|
T | A | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+4453T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103667 | ||||||
| chr12:103676
|
A | AGGGCTCA others(363): Show |
1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.623+4541_623+4542i others(372): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103676 | |||||
| chr12:103676
|
A | G | 11 | a0001c0003t0001g0101a0001c0004t0012g0021a0001c0004t0012g0022others(8): Show | 11 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.623+4462A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103676 | ||||||
| chr12:103679
|
G | GCTCAGGA others(107): Show |
1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.623+4471_623+4472i others(116): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103679 | |||||
| chr12:103682
|
C | CG | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+4468_623+4469i others(3): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103682 | ||||||
| chr12:103683
|
A | AGGAGGGA others(145): Show |
1 | a0001c0003t0001g0101 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.623+4471_623+4472i others(154): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103683 | |||||
| chr12:103683
|
A | AGGGGTAG others(147): Show |
1 | a0001c0006t0049g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.623+4497_623+4498i others(156): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103683 | |||||
| chr12:103683
|
A | G | 12 | a0001c0004t0011g0200a0001c0004t0012g0021a0001c0004t0012g0022others(9): Show | 12 | HG00438.hp1 HG01074.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.623+4469A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103683 | ||||||
| chr12:103688
|
T | G | 5 | a0001c0004t0011g0200a0002c0001t0051g0013a0002c0009t0002g0213others(2): Show | 5 | HG00438.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.623+4474T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103688 | ||||||
| chr12:103707
|
G | A | 9 | a0001c0002t0003g0174a0001c0003t0002g0169a0001c0003t0011g0138others(6): Show | 9 | HG00597.hp2 HG00621.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.623+4493G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103707 | ||||||
| chr12:103712
|
T | C | 5 | a0001c0002t0002g0240a0002c0001t0011g0124a0007c0021t0001g0230others(2): Show | 5 | HG01081.hp1 HG01175.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.623+4498T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103712 | ||||||
| chr12:103712
|
T | TGGGGCTC others(31): Show |
2 | a0001c0004t0011g0200a0002c0009t0002g0213 | 2 | HG00438.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.623+4501_623+4502i others(40): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103712 | |||||
| chr12:103713
|
G | GGGACTCA others(1249): Show |
1 | a0004c0011t0003g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.623+4555_623+4556i others(1258): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103713 | |||||
| chr12:103716
|
A | ACTCAGGA others(104): Show |
1 | a0001c0059t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.623+4555_623+4556i others(113): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103716 | |||||
| chr12:103716
|
A | ACTCAGGA others(104): Show |
39 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0218others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.623+4555_623+4556i others(113): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103716 | |||||
| chr12:103716
|
A | ACTCAGGA others(624): Show |
1 | a0003c0005t0002g0252 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.623+4555_623+4556i others(633): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103716 | |||||
| chr12:103716
|
A | G | 9 | a0001c0002t0002g0240a0001c0004t0011g0200a0002c0001t0011g0124others(6): Show | 9 | HG00438.hp1 HG01081.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.623+4502A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103716 | ||||||
| chr12:103723
|
A | C | 2 | a0007c0048t0001g0221a0007c0050t0010g0220 | 2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.623+4509A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103723 | ||||||
| chr12:103724
|
G | A | 2 | a0007c0048t0001g0221a0007c0050t0010g0220 | 2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.623+4510G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103724 | ||||||
| chr12:103739
|
C | CA | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+4525_623+4526i others(3): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103739 | ||||||
| chr12:103739
|
C | CAGGGGGG others(105): Show |
2 | a0007c0048t0001g0221a0007c0050t0010g0220 | 2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.623+4525_623+4526i others(114): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103739 | ||||||
| chr12:103739
|
C | T | 2 | a0002c0001t0024g0017a0002c0015t0031g0207 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.623+4525C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103739 | ||||||
| chr12:103740
|
G | GGGGGGAG others(66): Show |
1 | a0002c0001t0011g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.623+4555_623+4556i others(75): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103740 | |||||
| chr12:103741
|
G | T | 2 | a0007c0048t0001g0221a0007c0050t0010g0220 | 2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.623+4527G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103741 | ||||||
| chr12:103765
|
T | C | 12 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(9): Show | 12 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.623+4551T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103765 | ||||||
| chr12:103773
|
A | T | 12 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(9): Show | 12 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.623+4559A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103773 | ||||||
| chr12:103792
|
A | AGGGGGGA others(141): Show |
8 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(5): Show | 8 | HG01074.hp1 HG02257.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.623+4580_623+4581i others(150): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103792 | |||||
| chr12:103793
|
G | GGGGGGAG others(325): Show |
1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.623+4580_623+4581i others(334): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103793 | |||||
| chr12:103795
|
C | G | 12 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(9): Show | 12 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.623+4581C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103795 | ||||||
| chr12:103796
|
A | G | 2 | a0001c0006t0049g0144a0002c0001t0008g0026 | 2 | HG01358.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.623+4582A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103796 | ||||||
| chr12:103799
|
A | AGGCGGGG others(47): Show |
1 | a0001c0006t0049g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.623+4586_623+4587i others(56): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103799 | |||||
| chr12:103799
|
A | G | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(7): Show | 10 | HG01074.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.623+4585A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103799 | ||||||
| chr12:103801
|
A | G | 1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.623+4587A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103801 | ||||||
| chr12:103802
|
C | G | 269 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.623+4588C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103802 | ||||||
| chr12:103804
|
T | C | 11 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(8): Show | 11 | HG01074.hp1 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.623+4590T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103804 | ||||||
| chr12:103804
|
T | G | 1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.623+4590T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103804 | ||||||
| chr12:103805
|
G | GGCTCAGG others(10): Show |
1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.623+4592_623+4593i others(19): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103805 | |||||
| chr12:103808
|
A | G | 11 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(8): Show | 11 | HG01074.hp1 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.623+4594A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103808 | ||||||
| chr12:103809
|
C | G | 1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.623+4595C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103809 | ||||||
| chr12:103811
|
C | T | 1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.623+4597C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103811 | ||||||
| chr12:103812
|
A | C | 1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.623+4598A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103812 | ||||||
| chr12:103812
|
A | G | 8 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(5): Show | 8 | HG01074.hp1 HG02257.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.623+4598A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103812 | ||||||
| chr12:103812
|
A | T | 1 | a0002c0001t0005g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623+4598A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103812 | ||||||
| chr12:103815
|
T | A | 9 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(6): Show | 9 | HG01074.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.623+4601T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103815 | ||||||
| chr12:103824
|
A | AGGGCTCA others(30): Show |
8 | a0001c0041t0056g0072a0002c0001t0001g0191a0002c0001t0022g0087others(5): Show | 8 | HG01106.hp1 HG01952.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.623+4612_623+4613i others(39): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103824 | |||||
| chr12:103824
|
A | G | 11 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(8): Show | 11 | HG01074.hp1 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.623+4610A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103824 | ||||||
| chr12:103827
|
A | G | 12 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(9): Show | 12 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.623+4613A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103827 | ||||||
| chr12:103831
|
A | G | 1 | a0002c0001t0005g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623+4617A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103831 | ||||||
| chr12:103831
|
A | T | 9 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(6): Show | 9 | HG01074.hp1 HG02257.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.623+4617A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103831 | ||||||
| chr12:103836
|
G | A | 1 | a0001c0004t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.623+4622G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103836 | ||||||
| chr12:103837
|
GA | G | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(7): Show | 10 | HG01074.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.623+4624delA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103837 | ||||||
| chr12:103838
|
A | G | 1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.623+4624A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103838 | ||||||
| chr12:103843
|
T | C | 11 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(8): Show | 11 | HG01074.hp1 HG01358.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.623+4629T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103843 | ||||||
| chr12:103846
|
A | G | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.623+4632A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103846 | ||||||
| chr12:103848
|
T | C | 10 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0006t0049g0144others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.623+4634T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103848 | ||||||
| chr12:103848
|
T | G | 1 | a0002c0001t0005g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623+4634T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103848 | ||||||
| chr12:103848
|
T | TTCGGTGG others(232): Show |
1 | a0001c0007t0001g0103 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.623+4636_623+4637i others(241): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103848 | |||||
| chr12:103848
|
T | TTCGGTGG others(271): Show |
1 | a0003c0017t0015g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.623+4636_623+4637i others(280): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103848 | |||||
| chr12:103849
|
T | G | 1 | a0002c0001t0005g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623+4635T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103849 | ||||||
| chr12:103850
|
CAT | C | 8 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(5): Show | 8 | HG01074.hp1 HG02257.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.623+4637_623+4638d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103850 | ||||||
| chr12:103851
|
A | AGTGGGGA others(759): Show |
1 | a0007c0021t0001g0230 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.623+4637_623+4638i others(768): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103851 | ||||||
| chr12:103851
|
A | AGTGGGGA others(1223): Show |
1 | a0013c0022t0001g0259 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.623+4637_623+4638i others(1232): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103851 | ||||||
| chr12:103851
|
A | T | 5 | a0001c0006t0049g0144a0001c0007t0001g0103a0002c0001t0005g0054others(2): Show | 5 | HG01358.hp1 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.623+4637A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103851 | ||||||
| chr12:103852
|
T | C | 1 | a0002c0001t0005g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623+4638T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103852 | ||||||
| chr12:103852
|
T | G | 271 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.623+4638T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103852 | ||||||
| chr12:103854
|
A | G | 9 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(6): Show | 9 | HG01074.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.623+4640A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103854 | ||||||
| chr12:103854
|
A | T | 1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.623+4640A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103854 | ||||||
| chr12:103860
|
G | GGTGGGAC others(557): Show |
1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.623+4647_623+4648i others(566): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103860 | |||||
| chr12:103862
|
C | CAGGGCTC others(87): Show |
1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.623+4648_623+4649i others(96): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103862 | ||||||
| chr12:103862
|
C | CGG | 29 | a0001c0002t0002g0090a0001c0002t0002g0182a0001c0002t0055g0256others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.623+4649_623+4650d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGG | 9 | a0001c0004t0012g0021a0001c0004t0012g0022a0002c0001t0001g0019others(6): Show | 9 | HG01074.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(5): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(393): Show |
9 | a0001c0003t0005g0193a0001c0003t0007g0003a0001c0003t0007g0004others(6): Show | 9 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(402): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(394): Show |
1 | a0002c0001t0013g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(403): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(482): Show |
1 | a0002c0015t0046g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(491): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(503): Show |
1 | a0004c0008t0052g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(512): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(482): Show |
1 | a0001c0041t0056g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(491): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(390): Show |
6 | a0002c0001t0001g0191a0002c0001t0022g0087a0003c0005t0012g0074others(3): Show | 6 | HG01106.hp1 HG01952.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(399): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(390): Show |
1 | a0005c0018t0008g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(399): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(537): Show |
1 | a0001c0007t0001g0117 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(546): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(388): Show |
1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(397): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(312): Show |
5 | a0001c0004t0035g0030a0002c0001t0004g0027a0002c0001t0004g0028others(2): Show | 5 | HG01243.hp1 HG01516.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(321): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(313): Show |
1 | a0001c0004t0004g0031 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(322): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(1193): Show |
1 | a0005c0013t0025g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(1202): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(330): Show |
1 | a0001c0003t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(339): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(330): Show |
4 | a0001c0003t0001g0225a0002c0001t0020g0071a0008c0016t0007g0037others(1): Show | 4 | HG02622.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(339): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(274): Show |
1 | a0003c0005t0003g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(283): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(557): Show |
1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(566): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(328): Show |
1 | a0001c0004t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(337): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(330): Show |
16 | a0001c0002t0002g0167a0001c0003t0002g0060a0001c0004t0001g0053others(13): Show | 16 | HG01167.hp1 HG01981.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(339): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(387): Show |
1 | a0001c0024t0001g0032 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(396): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(592): Show |
1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(601): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(539): Show |
1 | a0001c0003t0001g0086 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(548): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(576): Show |
3 | a0001c0004t0003g0082a0002c0009t0002g0080a0002c0009t0002g0081 | 3 | HG01517.hp1 HG02273.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.623+4650_623+4651i others(585): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(612): Show |
1 | a0001c0043t0004g0063 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(621): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(595): Show |
98 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(95): Show | 99 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(604): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(634): Show |
2 | a0001c0007t0001g0150a0002c0001t0006g0151 | 2 | HG00438.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.623+4650_623+4651i others(643): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(614): Show |
3 | a0001c0003t0002g0169a0002c0001t0021g0163a0002c0001t0021g0164 | 3 | HG00621.hp1 NA18941.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.623+4650_623+4651i others(623): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(596): Show |
1 | a0001c0003t0012g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(605): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(595): Show |
1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(604): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(820): Show |
1 | a0001c0006t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(829): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(595): Show |
1 | a0001c0002t0002g0123 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(604): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(426): Show |
1 | a0001c0002t0002g0254 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(435): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(779): Show |
3 | a0001c0002t0002g0261a0001c0004t0016g0223a0001c0006t0002g0258 | 3 | HG00323.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.623+4650_623+4651i others(788): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(502): Show |
1 | a0023c0039t0030g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(511): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(274): Show |
4 | a0001c0003t0002g0219a0002c0001t0002g0047a0006c0012t0004g0065others(1): Show | 4 | HG02897.hp2 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(283): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(594): Show |
1 | a0001c0003t0001g0045 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(603): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(650): Show |
1 | a0002c0009t0002g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(659): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(427): Show |
1 | a0001c0004t0011g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(436): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(277): Show |
3 | a0001c0002t0002g0008a0002c0001t0005g0007a0003c0005t0009g0009 | 3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.623+4650_623+4651i others(286): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(615): Show |
2 | a0003c0005t0013g0036a0003c0005t0023g0245 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.623+4650_623+4651i others(624): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(274): Show |
1 | a0001c0003t0001g0101 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(283): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(557): Show |
1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(566): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(708): Show |
1 | a0005c0013t0009g0246 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(717): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(538): Show |
5 | a0003c0005t0019g0226a0003c0005t0028g0228a0003c0046t0001g0229others(2): Show | 5 | HG01346.hp2 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(547): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(557): Show |
1 | a0001c0003t0001g0267 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(566): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(517): Show |
1 | a0002c0009t0002g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(526): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(501): Show |
1 | a0005c0018t0001g0248 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(510): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(651): Show |
1 | a0001c0004t0037g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(660): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(501): Show |
1 | a0001c0004t0001g0235 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(510): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(501): Show |
1 | a0002c0009t0002g0262 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(510): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(501): Show |
18 | a0001c0002t0002g0240a0001c0002t0002g0257a0001c0006t0002g0145others(15): Show | 18 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(510): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(596): Show |
1 | a0001c0002t0002g0239 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(605): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(444): Show |
1 | a0001c0002t0002g0218 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(453): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(766): Show |
1 | a0002c0001t0011g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(775): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(500): Show |
1 | a0002c0001t0003g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(509): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(538): Show |
4 | a0001c0002t0002g0066a0002c0001t0008g0067a0003c0005t0023g0068others(1): Show | 4 | HG02109.hp2 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.623+4650_623+4651i others(547): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(595): Show |
1 | a0001c0004t0002g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(604): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(559): Show |
1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(568): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(576): Show |
1 | a0003c0005t0009g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(585): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(595): Show |
3 | a0001c0002t0002g0035a0003c0005t0009g0077a0003c0010t0012g0034 | 3 | HG01884.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.623+4650_623+4651i others(604): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(519): Show |
1 | a0009c0051t0001g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(528): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(502): Show |
1 | a0007c0048t0001g0221 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(511): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(502): Show |
1 | a0001c0059t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.623+4650_623+4651i others(511): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(577): Show |
1 | a0002c0001t0016g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(586): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(653): Show |
1 | a0004c0011t0003g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(662): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(317): Show |
1 | a0003c0005t0002g0252 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(326): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(442): Show |
1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(451): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(948): Show |
1 | a0002c0015t0031g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.623+4650_623+4651i others(957): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | CGGGGCTC others(333): Show |
2 | a0002c0015t0013g0018a0008c0016t0007g0058 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.623+4650_623+4651i others(342): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103862 | |||||
| chr12:103862
|
C | G | 1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.623+4648C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103862 | ||||||
| chr12:103868
|
G | A | 115 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(112): Show | 116 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.623+4654G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103868 | ||||||
| chr12:103868
|
G | GGGAGGGG others(12): Show |
1 | a0001c0003t0001g0101 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.623+4669_623+4670i others(21): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103868 | |||||
| chr12:103868
|
G | T | 119 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0002t0002g0066others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.623+4654G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103868 | ||||||
| chr12:103869
|
G | GGGGGTAG others(421): Show |
1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.623+4656_623+4657i others(430): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(290): Show |
2 | a0001c0037t0011g0194a0002c0001t0001g0195 | 2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.623+4656_623+4657i others(299): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(737): Show |
1 | a0002c0001t0011g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.623+4656_623+4657i others(746): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(231): Show |
1 | a0020c0047t0042g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.623+4656_623+4657i others(240): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(231): Show |
11 | a0001c0002t0002g0182a0001c0003t0010g0155a0001c0004t0001g0170others(8): Show | 11 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.623+4656_623+4657i others(240): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(884): Show |
1 | a0005c0031t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.623+4656_623+4657i others(893): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(901): Show |
1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+4656_623+4657i others(910): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(479): Show |
1 | a0001c0002t0055g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.623+4656_623+4657i others(488): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(498): Show |
1 | a0022c0038t0007g0255 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.623+4656_623+4657i others(507): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(231): Show |
1 | a0001c0004t0001g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.623+4656_623+4657i others(240): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
G | GGGGGTAG others(290): Show |
2 | a0007c0021t0004g0253a0016c0057t0014g0274 | 2 | HG00733.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.623+4656_623+4657i others(299): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103869
|
GGA | G | 5 | a0001c0006t0049g0144a0001c0007t0001g0103a0003c0017t0015g0056others(2): Show | 5 | HG01081.hp1 HG02717.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.623+4657_623+4658d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103869 | |||||
| chr12:103871
|
A | G | 23 | a0001c0002t0002g0090a0001c0002t0002g0182a0001c0002t0055g0256others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.623+4657A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103871 | ||||||
| chr12:103879
|
CG | C | 23 | a0001c0002t0002g0008a0001c0003t0005g0193a0001c0003t0007g0003others(20): Show | 23 | HG01106.hp1 HG01891.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.623+4670delG | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103879 | |||||
| chr12:103880
|
G | GGGGCTCT others(218): Show |
1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.623+4669_623+4670i others(227): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103880 | |||||
| chr12:103888
|
G | GGGGGGGG others(86): Show |
1 | a0002c0001t0005g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623+4676_623+4677i others(95): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 103888 | |||||
| chr12:103888
|
G | T | 28 | a0001c0002t0002g0090a0001c0002t0002g0182a0001c0002t0055g0256others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.623+4674G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103888 | ||||||
| chr12:103890
|
GA | G | 22 | a0001c0002t0002g0008a0001c0003t0005g0193a0001c0003t0007g0003others(19): Show | 22 | HG01106.hp1 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.623+4677delA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103890 | ||||||
| chr12:103891
|
A | G | 86 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0167others(83): Show | 86 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.623+4677A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103891 | ||||||
| chr12:103983
|
A | G | 2 | a0001c0007t0001g0103a0003c0017t0015g0056 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.623+4769A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 103983 | ||||||
| chr12:104184
|
A | G | 2 | a0002c0001t0024g0017a0002c0015t0031g0207 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.623+4970A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 104184 | ||||||
| chr12:104195
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+4981A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 104195 | ||||||
| chr12:104541
|
T | C | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.623+5327T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 104541 | ||||||
| chr12:104559
|
T | A | 4 | a0001c0004t0001g0170a0002c0001t0002g0047a0002c0015t0031g0207others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+5345T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 104559 | ||||||
| chr12:104559
|
T | TA | 127 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(124): Show | 128 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.623+5355dupA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 104559 | |||||
| chr12:104567
|
A | G | 2 | a0003c0005t0013g0036a0003c0005t0023g0245 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.623+5353A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 104567 | ||||||
| chr12:104752
|
G | A | 1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.623+5538G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 104752 | ||||||
| chr12:104832
|
A | G | 46 | a0001c0002t0002g0090a0001c0002t0002g0218a0001c0002t0002g0239others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.623+5618A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 104832 | ||||||
| chr12:104837
|
C | G | 24 | a0001c0003t0005g0193a0001c0003t0007g0004a0001c0041t0056g0072others(21): Show | 24 | HG01106.hp1 HG01891.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.623+5623C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 104837 | ||||||
| chr12:105365
|
T | G | 1 | a0002c0001t0003g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.623+6151T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 105365 | ||||||
| chr12:105389
|
G | C | 53 | a0001c0002t0002g0066a0001c0002t0002g0218a0001c0002t0002g0239others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.623+6175G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 105389 | ||||||
| chr12:105390
|
C | A | 53 | a0001c0002t0002g0066a0001c0002t0002g0218a0001c0002t0002g0239others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.623+6176C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 105390 | ||||||
| chr12:105568
|
C | A | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+6354C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 105568 | ||||||
| chr12:105846
|
G | A | 8 | a0001c0003t0039g0116a0001c0004t0002g0142a0001c0004t0003g0197others(5): Show | 8 | HG02015.hp2 HG02056.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.623+6632G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 105846 | ||||||
| chr12:105955
|
G | A | 51 | a0001c0002t0002g0066a0001c0002t0002g0218a0001c0002t0002g0239others(48): Show | 51 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.623+6741G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 105955 | ||||||
| chr12:105970
|
T | G | 2 | a0002c0001t0050g0051a0005c0031t0001g0057 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.623+6756T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 105970 | ||||||
| chr12:106046
|
C | T | 1 | a0001c0003t0001g0267 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.623+6832C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 106046 | ||||||
| chr12:106049
|
G | C | 30 | a0001c0002t0002g0035a0001c0002t0002g0090a0001c0002t0002g0182others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.623+6835G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 106049 | ||||||
| chr12:106694
|
G | A | 2 | a0002c0001t0024g0017a0002c0015t0031g0207 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.623+7480G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 106694 | ||||||
| chr12:106750
|
C | T | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.623+7536C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 106750 | ||||||
| chr12:106783
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+7569A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 106783 | ||||||
| chr12:106873
|
T | C | 124 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(121): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.623+7659T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 106873 | ||||||
| chr12:106895
|
AG | A | 13 | a0001c0003t0039g0116a0001c0004t0002g0142a0001c0004t0003g0197others(10): Show | 13 | HG00597.hp1 HG00621.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.623+7684delG | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 106895 | |||||
| chr12:107044
|
A | G | 125 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(122): Show | 126 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.623+7830A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107044 | ||||||
| chr12:107068
|
G | A | 124 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(121): Show | 125 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.623+7854G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107068 | ||||||
| chr12:107114
|
C | T | 1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.623+7900C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107114 | ||||||
| chr12:107402
|
C | CT | 139 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0090others(136): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.623+8213dupT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 107402 | |||||
| chr12:107402
|
C | CTT | 36 | a0001c0002t0002g0035a0001c0002t0002g0096a0001c0002t0002g0098others(33): Show | 36 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.623+8212_623+8213d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 107402 | |||||
| chr12:107402
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.623+8204_623+8213d others(12): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 107402 | |||||
| chr12:107402
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0001t0011g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.623+8199_623+8213d others(17): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 107402 | |||||
| chr12:107410
|
T | TC | 4 | a0001c0003t0001g0225a0002c0001t0020g0071a0008c0016t0007g0037others(1): Show | 4 | HG02622.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+8196_623+8197i others(3): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107410 | ||||||
| chr12:107534
|
C | G | 1 | a0009c0020t0001g0238 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.623+8320C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107534 | ||||||
| chr12:107534
|
C | T | 11 | a0001c0003t0001g0088a0001c0003t0001g0111a0001c0003t0001g0126others(8): Show | 11 | HG01346.hp1 HG01496.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.623+8320C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107534 | ||||||
| chr12:107553
|
G | A | 25 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0003t0002g0060others(22): Show | 25 | HG01074.hp1 HG01167.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.623+8339G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107553 | ||||||
| chr12:107554
|
T | C | 25 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0003t0002g0060others(22): Show | 25 | HG01074.hp1 HG01167.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.623+8340T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107554 | ||||||
| chr12:107559
|
G | A | 25 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0003t0002g0060others(22): Show | 25 | HG01074.hp1 HG01167.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.623+8345G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107559 | ||||||
| chr12:107564
|
C | T | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.623+8350C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107564 | ||||||
| chr12:107600
|
C | T | 1 | a0001c0004t0011g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.623+8386C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107600 | ||||||
| chr12:107611
|
T | G | 1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.623+8397T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107611 | ||||||
| chr12:107635
|
C | T | 1 | a0002c0001t0011g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.623+8421C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107635 | ||||||
| chr12:107645
|
C | T | 1 | a0002c0001t0003g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.623+8431C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107645 | ||||||
| chr12:107657
|
A | G | 136 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(133): Show | 137 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.623+8443A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107657 | ||||||
| chr12:107684
|
A | C | 2 | a0001c0002t0002g0167a0001c0041t0056g0072 | 2 | HG03209.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.623+8470A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107684 | ||||||
| chr12:107702
|
G | A | 2 | a0001c0003t0012g0049a0003c0010t0007g0268 | 2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.623+8488G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107702 | ||||||
| chr12:107705
|
C | T | 1 | a0003c0010t0012g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.623+8491C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107705 | ||||||
| chr12:107796
|
C | T | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.623+8582C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107796 | ||||||
| chr12:107862
|
A | G | 274 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.623+8648A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107862 | ||||||
| chr12:107888
|
G | A | 280 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.623+8674G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 107888 | ||||||
| chr12:108029
|
G | A | 4 | a0002c0001t0050g0051a0002c0015t0013g0018a0005c0031t0001g0057others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.623+8815G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108029 | ||||||
| chr12:108091
|
T | TCCCTAA | 7 | a0002c0001t0051g0013a0002c0015t0013g0018a0003c0005t0002g0252others(4): Show | 7 | HG01167.hp2 HG01346.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.623+8907_623+8912d others(8): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 108091 | |||||
| chr12:108133
|
A | G | 1 | a0001c0004t0060g0217 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.623+8919A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108133 | ||||||
| chr12:108196
|
C | G | 2 | a0001c0002t0002g0218a0001c0002t0002g0239 | 2 | HG00408.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.623+8982C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108196 | ||||||
| chr12:108217
|
A | T | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.623+9003A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108217 | ||||||
| chr12:108260
|
T | C | 127 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(124): Show | 128 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.623+9046T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108260 | ||||||
| chr12:108288
|
G | A | 1 | a0002c0001t0005g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.623+9074G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108288 | ||||||
| chr12:108316
|
A | T | 238 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(235): Show | 239 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.623+9102A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108316 | ||||||
| chr12:108450
|
G | A | 6 | a0001c0004t0001g0091a0001c0024t0001g0032a0001c0037t0011g0194others(3): Show | 6 | HG01123.hp2 HG01884.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+9236G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108450 | ||||||
| chr12:108598
|
A | G | 6 | a0001c0004t0001g0091a0001c0024t0001g0032a0001c0037t0011g0194others(3): Show | 6 | HG01123.hp2 HG01884.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+9384A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108598 | ||||||
| chr12:108692
|
G | C | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+9478G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108692 | ||||||
| chr12:108763
|
C | T | 1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.623+9549C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108763 | ||||||
| chr12:108796
|
T | C | 129 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(126): Show | 130 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.623+9582T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108796 | ||||||
| chr12:108858
|
G | T | 127 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(124): Show | 128 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.623+9644G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108858 | ||||||
| chr12:108985
|
C | T | 4 | a0001c0003t0001g0225a0002c0001t0020g0071a0008c0016t0007g0037others(1): Show | 4 | HG02622.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+9771C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108985 | ||||||
| chr12:108986
|
G | A | 35 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0003t0002g0060others(32): Show | 35 | HG01074.hp1 HG01167.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.623+9772G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 108986 | ||||||
| chr12:109001
|
C | T | 2 | a0002c0015t0013g0018a0008c0016t0007g0058 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.623+9787C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109001 | ||||||
| chr12:109084
|
C | T | 2 | a0001c0007t0001g0150a0002c0001t0006g0151 | 2 | HG00438.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.623+9870C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109084 | ||||||
| chr12:109086
|
C | T | 149 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0002t0002g0090others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.623+9872C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109086 | ||||||
| chr12:109088
|
C | A | 2 | a0002c0001t0002g0119a0002c0001t0002g0120 | 2 | NA18950.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.623+9874C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109088 | ||||||
| chr12:109225
|
C | T | 2 | a0001c0004t0058g0185a0001c0033t0013g0147 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.623+10011C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109225 | ||||||
| chr12:109286
|
C | T | 2 | a0002c0015t0013g0018a0008c0016t0007g0058 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.623+10072C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109286 | ||||||
| chr12:109297
|
C | T | 1 | a0002c0009t0002g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.623+10083C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109297 | ||||||
| chr12:109377
|
G | T | 1 | a0002c0001t0006g0151 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.623+10163G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109377 | ||||||
| chr12:109389
|
T | G | 23 | a0001c0002t0002g0008a0001c0003t0005g0193a0001c0003t0007g0003others(20): Show | 23 | HG01074.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.623+10175T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109389 | ||||||
| chr12:109400
|
G | A | 1 | a0005c0018t0001g0248 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.623+10186G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109400 | ||||||
| chr12:109413
|
C | A | 1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.623+10199C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109413 | ||||||
| chr12:109422
|
C | A | 70 | a0001c0002t0002g0182a0001c0002t0002g0218a0001c0002t0002g0239others(67): Show | 70 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.623+10208C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109422 | ||||||
| chr12:109432
|
T | A | 1 | a0005c0018t0008g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.623+10218T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109432 | ||||||
| chr12:109454
|
T | C | 1 | a0006c0012t0004g0065 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.623+10240T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109454 | ||||||
| chr12:109553
|
C | T | 177 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0090others(174): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.623+10339C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109553 | ||||||
| chr12:109604
|
A | G | 1 | a0001c0002t0002g0254 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.623+10390A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109604 | ||||||
| chr12:109616
|
CT | C | 70 | a0001c0002t0002g0035a0001c0002t0002g0167a0001c0002t0002g0218others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.623+10404delT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 109616 | |||||
| chr12:109618
|
T | C | 70 | a0001c0002t0002g0035a0001c0002t0002g0167a0001c0002t0002g0218others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.623+10404T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109618 | ||||||
| chr12:109687
|
G | T | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+10473G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109687 | ||||||
| chr12:109833
|
T | C | 4 | a0001c0003t0001g0088a0001c0003t0001g0126a0001c0003t0001g0172others(1): Show | 4 | HG01346.hp1 HG01975.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.623+10619T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109833 | ||||||
| chr12:109858
|
A | G | 1 | a0006c0012t0004g0065 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.623+10644A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109858 | ||||||
| chr12:109893
|
C | A | 15 | a0001c0004t0004g0031a0001c0004t0012g0021a0001c0004t0012g0022others(12): Show | 15 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.623+10679C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109893 | ||||||
| chr12:109946
|
C | A | 4 | a0001c0002t0002g0099a0001c0002t0002g0100a0001c0002t0002g0112others(1): Show | 4 | NA18962.hp1 NA18963.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+10732C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109946 | ||||||
| chr12:109970
|
A | T | 1 | a0001c0059t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.623+10756A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109970 | ||||||
| chr12:109984
|
C | T | 1 | a0001c0059t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.623+10770C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109984 | ||||||
| chr12:109992
|
C | T | 1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.623+10778C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 109992 | ||||||
| chr12:110025
|
T | C | 24 | a0001c0003t0001g0045a0001c0003t0002g0219a0001c0004t0004g0031others(21): Show | 24 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.623+10811T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110025 | ||||||
| chr12:110039
|
CCA | C | 5 | a0001c0004t0001g0091a0001c0024t0001g0032a0001c0037t0011g0194others(2): Show | 5 | HG01123.hp2 HG02738.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.623+10832_623+1083 others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 110039 | |||||
| chr12:110256
|
A | G | 15 | a0001c0004t0004g0031a0001c0004t0012g0021a0001c0004t0012g0022others(12): Show | 15 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.623+11042A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110256 | ||||||
| chr12:110293
|
C | A | 2 | a0001c0002t0002g0167a0001c0004t0001g0053 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.623+11079C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110293 | ||||||
| chr12:110315
|
G | C | 219 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(216): Show | 220 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.623+11101G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110315 | ||||||
| chr12:110399
|
C | T | 2 | a0003c0005t0013g0036a0003c0005t0023g0245 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.623+11185C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110399 | ||||||
| chr12:110400
|
G | A | 47 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.623+11186G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110400 | ||||||
| chr12:110654
|
C | T | 2 | a0001c0002t0002g0098a0001c0002t0002g0254 | 2 | HG00741.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.623+11440C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110654 | ||||||
| chr12:110669
|
T | C | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.623+11455T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110669 | ||||||
| chr12:110681
|
A | G | 1 | a0001c0043t0004g0063 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.623+11467A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110681 | ||||||
| chr12:110723
|
G | T | 2 | a0001c0002t0002g0218a0001c0002t0002g0239 | 2 | HG00408.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.623+11509G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110723 | ||||||
| chr12:110822
|
A | G | 164 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(161): Show | 165 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.623+11608A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110822 | ||||||
| chr12:110851
|
G | A | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+11637G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 110851 | ||||||
| chr12:111034
|
C | T | 1 | a0003c0005t0009g0077 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.623+11820C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111034 | ||||||
| chr12:111108
|
T | C | 4 | a0001c0003t0002g0169a0002c0001t0021g0163a0002c0001t0021g0164others(1): Show | 4 | HG00621.hp1 NA18941.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.623+11894T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111108 | ||||||
| chr12:111163
|
G | T | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.623+11949G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111163 | ||||||
| chr12:111197
|
G | C | 1 | a0001c0059t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.623+11983G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111197 | ||||||
| chr12:111242
|
A | C | 6 | a0001c0025t0040g0148a0003c0010t0019g0178a0006c0012t0001g0265others(3): Show | 6 | HG00673.hp2 HG01081.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.623+12028A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111242 | ||||||
| chr12:111274
|
A | G | 15 | a0001c0004t0004g0031a0001c0004t0012g0021a0001c0004t0012g0022others(12): Show | 15 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.623+12060A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111274 | ||||||
| chr12:111332
|
A | G | 1 | a0002c0001t0003g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.623+12118A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111332 | ||||||
| chr12:111372
|
G | A | 1 | a0001c0004t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.623+12158G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111372 | ||||||
| chr12:111630
|
C | T | 3 | a0003c0005t0009g0281a0003c0005t0013g0036a0003c0005t0023g0245 | 3 | HG02486.hp1 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.623+12416C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111630 | ||||||
| chr12:111636
|
G | A | 6 | a0001c0004t0001g0091a0001c0024t0001g0032a0001c0037t0011g0194others(3): Show | 6 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+12422G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111636 | ||||||
| chr12:111699
|
G | A | 1 | a0003c0046t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.623+12485G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111699 | ||||||
| chr12:111854
|
G | A | 36 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0182others(33): Show | 36 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.623+12640G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111854 | ||||||
| chr12:111939
|
T | A | 263 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.623+12725T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 111939 | ||||||
| chr12:112037
|
A | G | 227 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(224): Show | 228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.623+12823A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112037 | ||||||
| chr12:112045
|
G | A | 1 | a0001c0006t0002g0196 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.623+12831G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112045 | ||||||
| chr12:112173
|
A | G | 6 | a0001c0004t0001g0091a0001c0024t0001g0032a0001c0037t0011g0194others(3): Show | 6 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+12959A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112173 | ||||||
| chr12:112199
|
T | C | 1 | a0006c0012t0004g0065 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.623+12985T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112199 | ||||||
| chr12:112268
|
G | A | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.623+13054G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112268 | ||||||
| chr12:112318
|
A | T | 1 | a0001c0002t0002g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.623+13104A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112318 | ||||||
| chr12:112322
|
G | C | 1 | a0002c0001t0003g0181 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.623+13108G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112322 | ||||||
| chr12:112350
|
A | G | 2 | a0003c0005t0019g0226a0003c0005t0028g0228 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.623+13136A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112350 | ||||||
| chr12:112533
|
G | A | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.624-13100G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112533 | ||||||
| chr12:112794
|
G | C | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.624-12839G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 112794 | ||||||
| chr12:113006
|
G | C | 2 | a0001c0006t0010g0209a0001c0006t0010g0210 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.624-12627G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113006 | ||||||
| chr12:113095
|
GC | G | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-12533delC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 113095 | |||||
| chr12:113132
|
C | A | 6 | a0002c0001t0008g0020a0002c0001t0008g0023a0002c0001t0008g0025others(3): Show | 6 | HG01074.hp1 HG01358.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.624-12501C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113132 | ||||||
| chr12:113132
|
C | T | 1 | a0001c0002t0002g0123 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.624-12501C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113132 | ||||||
| chr12:113133
|
G | A | 2 | a0002c0001t0002g0143a0002c0001t0002g0171 | 2 | NA18994.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.624-12500G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113133 | ||||||
| chr12:113149
|
G | A | 2 | a0002c0001t0002g0260a0013c0022t0001g0237 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.624-12484G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113149 | ||||||
| chr12:113468
|
C | T | 8 | a0001c0003t0001g0225a0001c0044t0001g0050a0002c0001t0009g0064others(5): Show | 8 | HG02622.hp2 HG02970.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.624-12165C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113468 | ||||||
| chr12:113478
|
C | A | 6 | a0001c0002t0002g0001a0001c0002t0048g0105a0001c0003t0002g0102others(3): Show | 7 | HG00673.hp1 HG02027.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-12155C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113478 | ||||||
| chr12:113646
|
C | T | 10 | a0001c0003t0001g0045a0001c0003t0002g0219a0001c0004t0001g0091others(7): Show | 10 | HG01123.hp2 HG01993.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.624-11987C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113646 | ||||||
| chr12:113862
|
C | T | 1 | a0002c0001t0041g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.624-11771C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113862 | ||||||
| chr12:113975
|
G | T | 35 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0003g0174others(32): Show | 35 | HG00621.hp1 HG00673.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.624-11658G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 113975 | ||||||
| chr12:114003
|
A | G | 1 | a0007c0050t0010g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.624-11630A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114003 | ||||||
| chr12:114027
|
C | T | 53 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(50): Show | 53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.624-11606C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114027 | ||||||
| chr12:114092
|
C | T | 10 | a0001c0003t0001g0045a0001c0003t0002g0219a0001c0004t0001g0091others(7): Show | 10 | HG01123.hp2 HG01993.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.624-11541C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114092 | ||||||
| chr12:114177
|
C | T | 2 | a0003c0010t0015g0263a0003c0010t0015g0266 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.624-11456C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114177 | ||||||
| chr12:114256
|
G | C | 80 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0090others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.624-11377G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114256 | ||||||
| chr12:114490
|
G | C | 266 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.624-11143G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114490 | ||||||
| chr12:114532
|
A | G | 1 | a0001c0003t0004g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.624-11101A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114532 | ||||||
| chr12:114584
|
A | G | 1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.624-11049A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114584 | ||||||
| chr12:114799
|
T | G | 1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.624-10834T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114799 | ||||||
| chr12:114834
|
C | A | 43 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(40): Show | 43 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.624-10799C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114834 | ||||||
| chr12:114841
|
G | C | 2 | a0001c0044t0001g0050a0002c0001t0009g0064 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.624-10792G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114841 | ||||||
| chr12:114879
|
A | G | 2 | a0003c0005t0009g0281a0006c0012t0004g0065 | 2 | HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.624-10754A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114879 | ||||||
| chr12:114915
|
C | T | 13 | a0001c0003t0001g0267a0001c0003t0012g0049a0001c0041t0056g0072others(10): Show | 13 | HG01106.hp1 HG01952.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.624-10718C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 114915 | ||||||
| chr12:115044
|
A | T | 2 | a0001c0002t0002g0035a0001c0004t0002g0070 | 2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.624-10589A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115044 | ||||||
| chr12:115162
|
C | A | 18 | a0001c0003t0001g0267a0001c0003t0012g0049a0001c0041t0056g0072others(15): Show | 18 | HG01106.hp1 HG01952.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.624-10471C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115162 | ||||||
| chr12:115171
|
C | T | 61 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(58): Show | 62 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.624-10462C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115171 | ||||||
| chr12:115360
|
T | C | 15 | a0001c0004t0004g0031a0001c0004t0012g0021a0001c0004t0012g0022others(12): Show | 15 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.624-10273T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115360 | ||||||
| chr12:115365
|
T | C | 1 | a0024c0036t0057g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.624-10268T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115365 | ||||||
| chr12:115434
|
C | T | 6 | a0001c0004t0001g0091a0001c0024t0001g0032a0001c0037t0011g0194others(3): Show | 6 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-10199C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115434 | ||||||
| chr12:115479
|
C | A | 35 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0003g0174others(32): Show | 35 | HG00621.hp1 HG00673.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.624-10154C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115479 | ||||||
| chr12:115497
|
T | G | 51 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.624-10136T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115497 | ||||||
| chr12:115661
|
T | G | 4 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0004t0002g0070others(1): Show | 4 | HG01884.hp1 HG02109.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-9972T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115661 | ||||||
| chr12:115736
|
A | G | 132 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(129): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.624-9897A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115736 | ||||||
| chr12:115745
|
C | T | 90 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0218others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.624-9888C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115745 | ||||||
| chr12:115974
|
G | C | 2 | a0003c0005t0009g0281a0006c0012t0004g0065 | 2 | HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.624-9659G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 115974 | ||||||
| chr12:116010
|
T | A | 2 | a0003c0005t0009g0281a0006c0012t0004g0065 | 2 | HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.624-9623T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116010 | ||||||
| chr12:116023
|
G | C | 1 | a0002c0001t0001g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624-9610G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116023 | ||||||
| chr12:116108
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-9525C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116108 | ||||||
| chr12:116112
|
C | G | 2 | a0001c0006t0002g0092a0001c0006t0002g0196 | 2 | NA18975.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.624-9521C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116112 | ||||||
| chr12:116149
|
C | T | 14 | a0001c0003t0001g0267a0001c0003t0012g0049a0001c0041t0056g0072others(11): Show | 14 | HG01106.hp1 HG01952.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.624-9484C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116149 | ||||||
| chr12:116218
|
A | C | 187 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0002t0002g0066others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.624-9415A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116218 | ||||||
| chr12:116448
|
T | C | 177 | a0001c0002t0002g0008a0001c0002t0002g0090a0001c0002t0002g0167others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.624-9185T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116448 | ||||||
| chr12:116489
|
G | A | 44 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.624-9144G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116489 | ||||||
| chr12:116533
|
G | A | 62 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(59): Show | 63 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.624-9100G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116533 | ||||||
| chr12:116750
|
G | A | 65 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0099others(62): Show | 66 | HG00597.hp1 HG00621.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.624-8883G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 116750 | ||||||
| chr12:117309
|
G | A | 2 | a0002c0015t0013g0018a0008c0016t0007g0058 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.624-8324G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 117309 | ||||||
| chr12:117548
|
A | T | 1 | a0013c0022t0001g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.624-8085A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 117548 | ||||||
| chr12:117641
|
C | A | 63 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(60): Show | 64 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.624-7992C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 117641 | ||||||
| chr12:117763
|
A | G | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-7870A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 117763 | ||||||
| chr12:117895
|
G | A | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.624-7738G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 117895 | ||||||
| chr12:118757
|
G | A | 1 | a0003c0045t0045g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.624-6876G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 118757 | ||||||
| chr12:118812
|
T | G | 1 | a0002c0009t0002g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.624-6821T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 118812 | ||||||
| chr12:118898
|
C | T | 15 | a0001c0004t0004g0031a0001c0004t0012g0021a0001c0004t0012g0022others(12): Show | 15 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.624-6735C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 118898 | ||||||
| chr12:119414
|
G | A | 1 | a0002c0001t0003g0183 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624-6219G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 119414 | ||||||
| chr12:119459
|
A | G | 1 | a0003c0005t0059g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.624-6174A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 119459 | ||||||
| chr12:119605
|
A | G | 5 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0004t0002g0070others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.624-6028A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 119605 | ||||||
| chr12:119714
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-5919C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 119714 | ||||||
| chr12:119715
|
A | C | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-5918A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 119715 | ||||||
| chr12:119718
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-5915T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 119718 | ||||||
| chr12:119782
|
C | G | 171 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0090others(168): Show | 172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.624-5851C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 119782 | ||||||
| chr12:120008
|
C | A | 2 | a0003c0005t0023g0068a0003c0017t0002g0069 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.624-5625C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120008 | ||||||
| chr12:120107
|
C | T | 2 | a0003c0005t0009g0281a0006c0012t0004g0065 | 2 | HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.624-5526C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120107 | ||||||
| chr12:120130
|
A | C | 1 | a0002c0009t0002g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.624-5503A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120130 | ||||||
| chr12:120181
|
A | G | 261 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.624-5452A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120181 | ||||||
| chr12:120335
|
C | T | 8 | a0001c0003t0001g0225a0001c0044t0001g0050a0002c0001t0009g0064others(5): Show | 8 | HG02622.hp2 HG02970.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.624-5298C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120335 | ||||||
| chr12:120375
|
A | G | 37 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0003t0002g0060others(34): Show | 37 | HG00621.hp1 HG00673.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.624-5258A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120375 | ||||||
| chr12:120395
|
G | A | 235 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.624-5238G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120395 | ||||||
| chr12:120485
|
C | A | 48 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(45): Show | 48 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.624-5148C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120485 | ||||||
| chr12:120489
|
C | T | 48 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(45): Show | 48 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.624-5144C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120489 | ||||||
| chr12:120519
|
T | G | 265 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.624-5114T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120519 | ||||||
| chr12:120530
|
G | C | 1 | a0020c0047t0042g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.624-5103G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120530 | ||||||
| chr12:120554
|
G | C | 43 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(40): Show | 43 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.624-5079G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120554 | ||||||
| chr12:120781
|
G | C | 102 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0218others(99): Show | 102 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.624-4852G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120781 | ||||||
| chr12:120796
|
C | G | 2 | a0001c0003t0012g0049a0003c0010t0007g0268 | 2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.624-4837C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120796 | ||||||
| chr12:120886
|
G | A | 1 | a0026c0026t0003g0165 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.624-4747G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120886 | ||||||
| chr12:120964
|
T | C | 36 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0003t0002g0060others(33): Show | 36 | HG00621.hp1 HG00673.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.624-4669T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 120964 | ||||||
| chr12:121115
|
C | T | 152 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(149): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.624-4518C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 121115 | ||||||
| chr12:121121
|
G | A | 152 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(149): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.624-4512G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 121121 | ||||||
| chr12:121238
|
G | A | 155 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(152): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.624-4395G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 121238 | ||||||
| chr12:121423
|
G | A | 4 | a0006c0012t0001g0265a0006c0012t0005g0006a0006c0012t0032g0264others(1): Show | 4 | HG01081.hp2 HG01891.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.624-4210G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 121423 | ||||||
| chr12:121555
|
C | T | 34 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0003t0002g0060others(31): Show | 34 | HG00621.hp1 HG00673.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.624-4078C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 121555 | ||||||
| chr12:121583
|
G | A | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.624-4050G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 121583 | ||||||
| chr12:121643
|
A | C | 1 | a0002c0015t0031g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.624-3990A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 121643 | ||||||
| chr12:121795
|
G | A | 156 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(153): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.624-3838G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 121795 | ||||||
| chr12:122027
|
C | T | 9 | a0001c0003t0012g0049a0002c0001t0001g0191a0002c0001t0022g0087others(6): Show | 9 | HG01106.hp1 HG01952.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.624-3606C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122027 | ||||||
| chr12:122334
|
G | A | 156 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(153): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.624-3299G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122334 | ||||||
| chr12:122390
|
T | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0096others(63): Show | 67 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.624-3243T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122390 | ||||||
| chr12:122422
|
A | G | 156 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(153): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.624-3211A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122422 | ||||||
| chr12:122459
|
T | C | 4 | a0003c0005t0009g0281a0003c0005t0013g0036a0003c0005t0023g0245others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-3174T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122459 | ||||||
| chr12:122548
|
G | T | 1 | a0001c0041t0056g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.624-3085G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122548 | ||||||
| chr12:122643
|
G | A | 15 | a0001c0004t0004g0031a0001c0004t0012g0021a0001c0004t0012g0022others(12): Show | 15 | HG01074.hp1 HG01243.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.624-2990G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122643 | ||||||
| chr12:122652
|
G | C | 1 | a0002c0001t0001g0184 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.624-2981G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122652 | ||||||
| chr12:122654
|
G | A | 46 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(43): Show | 46 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.624-2979G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122654 | ||||||
| chr12:122738
|
G | A | 5 | a0002c0001t0003g0215a0002c0001t0011g0124a0002c0009t0002g0222others(2): Show | 5 | HG00735.hp2 HG01981.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.624-2895G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122738 | ||||||
| chr12:122751
|
G | A | 1 | a0004c0011t0003g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.624-2882G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122751 | ||||||
| chr12:122957
|
T | C | 162 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(159): Show | 163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.624-2676T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122957 | ||||||
| chr12:122996
|
G | A | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.624-2637G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 122996 | ||||||
| chr12:123092
|
A | G | 146 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0090others(143): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.624-2541A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123092 | ||||||
| chr12:123104
|
C | T | 4 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0004t0002g0070others(1): Show | 4 | HG01884.hp1 HG02109.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-2529C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123104 | ||||||
| chr12:123132
|
C | T | 1 | a0001c0025t0040g0148 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.624-2501C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123132 | ||||||
| chr12:123164
|
G | C | 1 | a0023c0039t0030g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.624-2469G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123164 | ||||||
| chr12:123188
|
C | T | 44 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.624-2445C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123188 | ||||||
| chr12:123235
|
T | A | 2 | a0001c0004t0016g0223a0001c0006t0002g0258 | 2 | HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.624-2398T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123235 | ||||||
| chr12:123253
|
A | G | 1 | a0002c0001t0008g0025 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.624-2380A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123253 | ||||||
| chr12:123308
|
G | A | 4 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0004t0002g0070others(1): Show | 4 | HG01884.hp1 HG02109.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-2325G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123308 | ||||||
| chr12:123413
|
C | G | 161 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(158): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.624-2220C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123413 | ||||||
| chr12:123460
|
A | T | 14 | a0001c0003t0012g0049a0001c0041t0056g0072a0002c0001t0001g0191others(11): Show | 14 | HG01081.hp2 HG01106.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.624-2173A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123460 | ||||||
| chr12:123538
|
C | T | 44 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.624-2095C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123538 | ||||||
| chr12:123561
|
G | A | 98 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0218others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.624-2072G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123561 | ||||||
| chr12:123648
|
T | G | 18 | a0001c0003t0012g0049a0001c0041t0056g0072a0001c0043t0004g0063others(15): Show | 18 | HG01081.hp2 HG01106.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.624-1985T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123648 | ||||||
| chr12:123686
|
G | A | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.624-1947G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123686 | ||||||
| chr12:123810
|
G | C | 165 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(162): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.624-1823G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123810 | ||||||
| chr12:123812
|
C | T | 1 | a0002c0001t0024g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.624-1821C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123812 | ||||||
| chr12:123817
|
A | T | 6 | a0001c0004t0001g0091a0001c0024t0001g0032a0001c0037t0011g0194others(3): Show | 6 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-1816A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123817 | ||||||
| chr12:123961
|
G | C | 2 | a0003c0005t0009g0281a0006c0012t0004g0065 | 2 | HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.624-1672G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 123961 | ||||||
| chr12:124036
|
G | A | 5 | a0001c0003t0007g0003a0002c0001t0013g0011a0002c0001t0024g0017others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.624-1597G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124036 | ||||||
| chr12:124086
|
A | G | 106 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0218others(103): Show | 106 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.624-1547A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124086 | ||||||
| chr12:124096
|
T | C | 105 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0218others(102): Show | 105 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.624-1537T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124096 | ||||||
| chr12:124103
|
T | C | 5 | a0001c0003t0001g0225a0002c0001t0020g0071a0002c0001t0051g0013others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.624-1530T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124103 | ||||||
| chr12:124109
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.624-1524G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124109 | ||||||
| chr12:124140
|
G | A | 1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.624-1493G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124140 | ||||||
| chr12:124157
|
C | T | 1 | a0001c0006t0049g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.624-1476C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124157 | ||||||
| chr12:124250
|
G | A | 99 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0218others(96): Show | 99 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.624-1383G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124250 | ||||||
| chr12:124381
|
C | T | 4 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0004t0002g0070others(1): Show | 4 | HG01884.hp1 HG02109.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1252C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124381 | ||||||
| chr12:124389
|
C | CA | 197 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.624-1228dupA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 124389 | |||||
| chr12:124389
|
C | CAA | 45 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0003t0002g0060others(42): Show | 45 | HG00621.hp1 HG00673.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.624-1229_624-1228d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 124389 | |||||
| chr12:124389
|
CA | C | 6 | a0001c0003t0007g0003a0001c0044t0001g0050a0002c0001t0009g0064others(3): Show | 6 | HG02145.hp1 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.624-1228delA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 124389 | |||||
| chr12:124620
|
C | A | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.624-1013C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124620 | ||||||
| chr12:124620
|
C | G | 48 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(45): Show | 48 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.624-1013C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124620 | ||||||
| chr12:124626
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0002g0219a0002c0001t0002g0047others(1): Show | 4 | HG01993.hp1 HG03704.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1007C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124626 | ||||||
| chr12:124708
|
C | T | 2 | a0001c0044t0001g0050a0002c0001t0009g0064 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.624-925C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124708 | ||||||
| chr12:124709
|
G | A | 6 | a0001c0004t0004g0031a0001c0004t0035g0030a0002c0001t0004g0027others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.624-924G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124709 | ||||||
| chr12:124833
|
T | C | 2 | a0001c0044t0001g0050a0002c0001t0009g0064 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.624-800T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 124833 | ||||||
| chr12:125013
|
C | G | 2 | a0002c0001t0002g0119a0002c0001t0002g0120 | 2 | NA18950.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.624-620C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125013 | ||||||
| chr12:125050
|
G | C | 135 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0125others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.624-583G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125050 | ||||||
| chr12:125083
|
T | C | 128 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0039others(125): Show | 129 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.624-550T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125083 | ||||||
| chr12:125111
|
C | T | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.624-522C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125111 | ||||||
| chr12:125129
|
G | A | 54 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(51): Show | 54 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.624-504G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125129 | ||||||
| chr12:125209
|
T | A | 44 | a0001c0002t0002g0218a0001c0002t0002g0239a0001c0002t0002g0240others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.624-424T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125209 | ||||||
| chr12:125247
|
G | C | 36 | a0001c0002t0002g0008a0001c0002t0002g0090a0001c0003t0002g0060others(33): Show | 36 | HG00621.hp1 HG00673.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.624-386G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125247 | ||||||
| chr12:125327
|
C | T | 1 | a0001c0003t0001g0267 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.624-306C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125327 | ||||||
| chr12:125328
|
G | A | 1 | a0001c0004t0037g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.624-305G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125328 | ||||||
| chr12:125353
|
G | A | 1 | a0002c0001t0013g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.624-280G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125353 | ||||||
| chr12:125381
|
C | T | 24 | a0001c0003t0002g0219a0001c0003t0005g0193a0001c0004t0004g0031others(21): Show | 24 | HG01123.hp2 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.624-252C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125381 | ||||||
| chr12:125388
|
GC | G | 4 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0004t0002g0070others(1): Show | 4 | HG01884.hp1 HG02109.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-242delC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 125388 | |||||
| chr12:125394
|
G | A | 133 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(130): Show | 134 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.624-239G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125394 | ||||||
| chr12:125395
|
C | T | 133 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(130): Show | 134 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.624-238C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125395 | ||||||
| chr12:125418
|
C | T | 1 | a0001c0002t0002g0099 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.624-215C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125418 | ||||||
| chr12:125446
|
T | A | 2 | a0001c0002t0002g0167a0001c0004t0001g0053 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.624-187T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125446 | ||||||
| chr12:125451
|
G | A | 1 | a0024c0036t0057g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.624-182G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125451 | ||||||
| chr12:125581
|
C | T | 2 | a0001c0003t0001g0225a0001c0007t0001g0075 | 2 | NA18747.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.624-52C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | chr12 | 125581 | ||||||
| chr12:125960
|
G | GC | 78 | a0001c0002t0002g0035a0001c0002t0002g0066a0001c0002t0002g0096others(75): Show | 78 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.903+49dupC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 125960 | |||||
| chr12:125962
|
T | C | 150 | a0001c0002t0002g0001a0001c0002t0002g0039a0001c0002t0002g0090others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.903+50T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 125962 | ||||||
| chr12:125965
|
G | T | 4 | a0002c0001t0004g0027a0002c0001t0004g0028a0002c0001t0004g0029others(1): Show | 4 | HG01243.hp1 HG01358.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+53G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 125965 | ||||||
| chr12:125976
|
A | G | 14 | a0001c0002t0002g0090a0001c0002t0002g0261a0001c0002t0055g0256others(11): Show | 14 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.903+64A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 125976 | ||||||
| chr12:125977
|
G | C | 82 | a0001c0002t0002g0090a0001c0002t0002g0096a0001c0002t0002g0100others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.903+65G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 125977 | ||||||
| chr12:126047
|
T | C | 1 | a0001c0002t0002g0240 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.903+135T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126047 | ||||||
| chr12:126167
|
A | T | 1 | a0002c0001t0036g0161 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.903+255A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126167 | ||||||
| chr12:126281
|
G | A | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.903+369G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126281 | ||||||
| chr12:126314
|
G | T | 29 | a0001c0002t0002g0090a0001c0002t0048g0105a0001c0003t0001g0044others(26): Show | 29 | HG00642.hp2 HG01175.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.903+402G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126314 | ||||||
| chr12:126427
|
G | T | 154 | a0001c0002t0002g0039a0001c0002t0002g0090a0001c0002t0002g0096others(151): Show | 154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.903+515G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126427 | ||||||
| chr12:126544
|
G | GGT | 24 | a0001c0002t0003g0174a0001c0003t0001g0044a0001c0003t0001g0086others(21): Show | 24 | HG00438.hp1 HG01346.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.903+660_903+661dup others(2): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGT | 34 | a0001c0003t0001g0176a0001c0003t0039g0116a0001c0004t0001g0053others(31): Show | 34 | HG00438.hp2 HG00621.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.903+658_903+661dup others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGT | 41 | a0001c0003t0001g0172a0001c0003t0012g0049a0001c0004t0004g0031others(38): Show | 41 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.903+656_903+661dup others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGTG others(1): Show |
21 | a0001c0002t0002g0008a0001c0002t0048g0105a0001c0003t0002g0102others(18): Show | 21 | HG01993.hp2 HG02155.hp2 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.903+654_903+661dup others(8): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGTG others(3): Show |
7 | a0001c0002t0002g0240a0001c0004t0001g0091a0001c0024t0001g0032others(4): Show | 7 | HG00323.hp2 HG01123.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+652_903+661dup others(10): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGTG others(5): Show |
4 | a0002c0015t0013g0018a0002c0040t0029g0156a0003c0005t0009g0009others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+650_903+661dup others(12): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGTG others(7): Show |
5 | a0001c0003t0002g0060a0001c0019t0034g0244a0002c0001t0050g0051others(2): Show | 5 | HG01168.hp1 HG02615.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+648_903+661dup others(14): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGTG others(9): Show |
8 | a0001c0002t0002g0167a0001c0002t0002g0182a0001c0003t0010g0155others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.903+646_903+661dup others(16): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGTG others(11): Show |
6 | a0001c0003t0002g0219a0001c0004t0058g0185a0001c0042t0001g0243others(3): Show | 6 | HG01255.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.903+644_903+661dup others(18): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGTG others(13): Show |
2 | a0001c0003t0001g0045a0001c0033t0013g0147 | 2 | HG01993.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.903+642_903+661dup others(20): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
G | GGTGTGTG others(17): Show |
3 | a0001c0006t0002g0095a0001c0019t0001g0139a0001c0034t0001g0214 | 3 | HG01070.hp2 NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.903+638_903+661dup others(24): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126544
|
GGTGT | G | 3 | a0001c0025t0040g0148a0003c0005t0062g0073a0014c0028t0001g0062 | 3 | HG00673.hp2 HG01167.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.903+658_903+661del others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 126544 | |||||
| chr12:126574
|
C | T | 45 | a0001c0002t0002g0240a0001c0003t0001g0044a0001c0003t0001g0086others(42): Show | 45 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.903+662C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126574 | ||||||
| chr12:126594
|
G | A | 95 | a0001c0002t0002g0167a0001c0002t0002g0182a0001c0002t0002g0240others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.903+682G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126594 | ||||||
| chr12:126672
|
A | C | 36 | a0001c0003t0011g0138a0001c0004t0003g0082a0001c0025t0040g0148others(33): Show | 36 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.903+760A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126672 | ||||||
| chr12:126716
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.903+804G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126716 | ||||||
| chr12:126736
|
A | C | 2 | a0002c0001t0009g0064a0006c0012t0004g0065 | 2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.903+824A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126736 | ||||||
| chr12:126796
|
G | A | 116 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0182others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.903+884G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126796 | ||||||
| chr12:126949
|
T | C | 29 | a0001c0002t0002g0167a0001c0002t0002g0182a0001c0002t0048g0105others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.903+1037T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126949 | ||||||
| chr12:126995
|
T | C | 6 | a0001c0002t0002g0008a0001c0004t0001g0091a0002c0001t0013g0011others(3): Show | 6 | HG02109.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+1083T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 126995 | ||||||
| chr12:127115
|
C | T | 85 | a0001c0002t0002g0008a0001c0002t0002g0240a0001c0003t0001g0044others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.903+1203C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127115 | ||||||
| chr12:127246
|
C | T | 1 | a0002c0040t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.903+1334C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127246 | ||||||
| chr12:127259
|
A | G | 31 | a0001c0002t0002g0008a0001c0003t0001g0045a0001c0003t0002g0219others(28): Show | 31 | HG01496.hp1 HG01516.hp2 HG01993.hp1 others(28): Show |
intron_variant | MODIFIER | c.903+1347A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127259 | ||||||
| chr12:127383
|
G | C | 3 | a0001c0044t0001g0050a0003c0005t0009g0055a0003c0010t0012g0034 | 3 | HG02970.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.903+1471G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127383 | ||||||
| chr12:127439
|
G | C | 3 | a0001c0004t0001g0091a0002c0001t0009g0064a0006c0012t0004g0065 | 3 | HG02897.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.903+1527G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127439 | ||||||
| chr12:127441
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.903+1529G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127441 | ||||||
| chr12:127464
|
C | G | 1 | a0002c0001t0011g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.903+1552C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127464 | ||||||
| chr12:127573
|
G | GA | 10 | a0001c0002t0002g0008a0001c0044t0001g0050a0002c0001t0013g0011others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+1672dupA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 127573 | |||||
| chr12:127588
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.903+1676G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127588 | ||||||
| chr12:127660
|
A | G | 1 | a0001c0019t0001g0139 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.903+1748A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127660 | ||||||
| chr12:127668
|
C | T | 13 | a0001c0002t0002g0008a0001c0004t0060g0217a0001c0044t0001g0050others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.903+1756C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127668 | ||||||
| chr12:127691
|
G | A | 13 | a0001c0002t0002g0008a0001c0004t0060g0217a0001c0044t0001g0050others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.903+1779G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127691 | ||||||
| chr12:127723
|
T | G | 23 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0012g0049others(20): Show | 23 | HG01496.hp1 HG01516.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.903+1811T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127723 | ||||||
| chr12:127757
|
A | G | 1 | a0002c0001t0003g0216 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.903+1845A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127757 | ||||||
| chr12:127770
|
G | T | 3 | a0001c0043t0004g0063a0008c0016t0007g0058a0008c0016t0061g0015 | 3 | HG02280.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.903+1858G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127770 | ||||||
| chr12:127797
|
G | A | 10 | a0001c0002t0002g0008a0001c0004t0060g0217a0002c0001t0013g0011others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+1885G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127797 | ||||||
| chr12:127832
|
G | C | 67 | a0001c0002t0002g0008a0001c0002t0002g0240a0001c0003t0001g0044others(64): Show | 67 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.903+1920G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127832 | ||||||
| chr12:127852
|
C | A | 2 | a0001c0002t0002g0261a0002c0001t0003g0041 | 2 | HG00323.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.903+1940C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127852 | ||||||
| chr12:127866
|
G | A | 67 | a0001c0002t0002g0008a0001c0002t0002g0240a0001c0003t0001g0044others(64): Show | 67 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.903+1954G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127866 | ||||||
| chr12:127931
|
A | G | 1 | a0001c0004t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.903+2019A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 127931 | ||||||
| chr12:128016
|
C | T | 1 | a0001c0004t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.903+2104C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128016 | ||||||
| chr12:128020
|
C | T | 30 | a0001c0002t0002g0167a0001c0002t0048g0105a0001c0003t0002g0060others(27): Show | 30 | HG00408.hp2 HG01106.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.903+2108C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128020 | ||||||
| chr12:128058
|
A | G | 1 | a0004c0011t0004g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.903+2146A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128058 | ||||||
| chr12:128073
|
G | A | 1 | a0002c0015t0031g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.903+2161G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128073 | ||||||
| chr12:128217
|
C | CT | 14 | a0001c0002t0002g0008a0001c0004t0060g0217a0001c0043t0004g0063others(11): Show | 14 | HG02109.hp1 HG02280.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.903+2305_903+2306i others(3): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128217 | ||||||
| chr12:128238
|
T | C | 82 | a0001c0002t0002g0008a0001c0002t0002g0240a0001c0002t0048g0105others(79): Show | 82 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.903+2326T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128238 | ||||||
| chr12:128278
|
A | G | 3 | a0001c0044t0001g0050a0003c0005t0009g0055a0003c0010t0012g0034 | 3 | HG02970.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.903+2366A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128278 | ||||||
| chr12:128298
|
A | G | 12 | a0001c0002t0002g0008a0001c0004t0060g0217a0001c0044t0001g0050others(9): Show | 12 | HG02109.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+2386A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128298 | ||||||
| chr12:128355
|
G | A | 215 | a0001c0002t0002g0008a0001c0002t0002g0090a0001c0002t0002g0167others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.903+2443G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128355 | ||||||
| chr12:128503
|
C | T | 1 | a0002c0015t0031g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.903+2591C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128503 | ||||||
| chr12:128514
|
G | T | 1 | a0008c0035t0007g0135 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.903+2602G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128514 | ||||||
| chr12:128515
|
A | C | 1 | a0008c0035t0007g0135 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.903+2603A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128515 | ||||||
| chr12:128517
|
GGGTGTTG others(7): Show |
G | 1 | a0008c0035t0007g0135 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.903+2606_903+2619d others(16): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128517 | ||||||
| chr12:128553
|
C | A | 1 | a0022c0038t0007g0255 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.903+2641C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128553 | ||||||
| chr12:128575
|
C | T | 1 | a0002c0001t0003g0041 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.903+2663C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128575 | ||||||
| chr12:128594
|
G | T | 63 | a0001c0002t0002g0240a0001c0003t0001g0044a0001c0003t0001g0045others(60): Show | 63 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.903+2682G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128594 | ||||||
| chr12:128747
|
C | T | 1 | a0002c0015t0031g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.903+2835C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128747 | ||||||
| chr12:128748
|
G | A | 1 | a0002c0009t0002g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.903+2836G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 128748 | ||||||
| chr12:129025
|
T | A | 148 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0182others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.903+3113T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129025 | ||||||
| chr12:129127
|
C | T | 1 | a0001c0002t0002g0125 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.903+3215C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129127 | ||||||
| chr12:129261
|
G | A | 100 | a0001c0002t0002g0008a0001c0002t0002g0182a0001c0002t0002g0240others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.903+3349G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129261 | ||||||
| chr12:129357
|
G | A | 2 | a0008c0016t0007g0058a0008c0016t0061g0015 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.903+3445G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129357 | ||||||
| chr12:129402
|
C | G | 66 | a0001c0002t0002g0008a0001c0002t0002g0240a0001c0003t0001g0044others(63): Show | 66 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.903+3490C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129402 | ||||||
| chr12:129482
|
G | A | 34 | a0001c0002t0002g0167a0001c0002t0048g0105a0001c0003t0002g0060others(31): Show | 34 | HG00408.hp2 HG01106.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.903+3570G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129482 | ||||||
| chr12:129527
|
C | T | 1 | a0001c0004t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.903+3615C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129527 | ||||||
| chr12:129598
|
C | G | 2 | a0008c0016t0007g0058a0008c0016t0061g0015 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.903+3686C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129598 | ||||||
| chr12:129605
|
G | GA | 108 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0240others(105): Show | 108 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.903+3695dupA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 129605 | |||||
| chr12:129608
|
T | C | 1 | a0001c0002t0002g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.903+3696T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129608 | ||||||
| chr12:129782
|
G | A | 1 | a0006c0012t0004g0065 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.903+3870G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129782 | ||||||
| chr12:129977
|
G | A | 37 | a0001c0002t0002g0240a0001c0003t0001g0172a0001c0006t0002g0136others(34): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.903+4065G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 129977 | ||||||
| chr12:130092
|
G | A | 6 | a0001c0004t0012g0021a0001c0004t0012g0022a0001c0004t0058g0185others(3): Show | 6 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.903+4180G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130092 | ||||||
| chr12:130135
|
G | C | 99 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0002g0240others(96): Show | 99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.903+4223G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130135 | ||||||
| chr12:130395
|
A | T | 3 | a0001c0004t0004g0031a0001c0004t0035g0030a0024c0036t0057g0048 | 3 | HG01496.hp1 HG01516.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.903+4483A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130395 | ||||||
| chr12:130446
|
C | T | 1 | a0004c0011t0004g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.903+4534C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130446 | ||||||
| chr12:130463
|
A | C | 1 | a0001c0003t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.903+4551A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130463 | ||||||
| chr12:130539
|
G | A | 1 | a0002c0001t0016g0121 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.903+4627G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130539 | ||||||
| chr12:130621
|
C | T | 82 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0002t0002g0066others(79): Show | 82 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.903+4709C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130621 | ||||||
| chr12:130678
|
C | A | 19 | a0001c0002t0002g0167a0001c0002t0048g0105a0001c0003t0002g0060others(16): Show | 19 | HG00408.hp2 HG01106.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.903+4766C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130678 | ||||||
| chr12:130688
|
T | C | 109 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0002t0002g0066others(106): Show | 109 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.903+4776T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130688 | ||||||
| chr12:130696
|
A | G | 2 | a0008c0016t0007g0058a0008c0016t0061g0015 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.903+4784A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130696 | ||||||
| chr12:130966
|
G | GCCCCCCA others(48): Show |
6 | a0001c0002t0002g0123a0001c0004t0001g0170a0002c0001t0002g0260others(3): Show | 6 | HG02083.hp1 HG02109.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.903+5056_903+5110d others(57): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 130966 | |||||
| chr12:130968
|
CCCCCACA others(48): Show |
C | 2 | a0008c0016t0007g0058a0008c0016t0061g0015 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.903+5067_903+5121d others(57): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 130968 | |||||
| chr12:130970
|
C | T | 2 | a0002c0001t0002g0119a0002c0001t0002g0120 | 2 | NA18950.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.903+5058C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130970 | ||||||
| chr12:130971
|
C | T | 3 | a0001c0003t0001g0225a0001c0003t0012g0049a0008c0016t0007g0037 | 3 | HG02055.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.903+5059C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 130971 | ||||||
| chr12:130986
|
A | ATCCTCAG others(160): Show |
1 | a0003c0010t0007g0268 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.903+5110_903+5111i others(169): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 130986 | |||||
| chr12:130986
|
A | ATCCTCAG others(49): Show |
5 | a0001c0003t0001g0086a0001c0003t0001g0111a0002c0001t0003g0234others(2): Show | 5 | HG00741.hp1 HG01934.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+5118_903+5173d others(58): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 130986 | |||||
| chr12:130986
|
A | ATCCTCAG others(216): Show |
1 | a0002c0001t0006g0175 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.903+5173_903+5174i others(225): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 130986 | |||||
| chr12:130986
|
A | ATCCTCAG others(105): Show |
3 | a0001c0003t0001g0141a0001c0003t0001g0176a0003c0005t0009g0055 | 3 | HG01496.hp2 NA18906.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.903+5173_903+5174i others(114): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 130986 | |||||
| chr12:130986
|
A | ATCCTCAG others(161): Show |
4 | a0001c0003t0001g0172a0001c0003t0033g0110a0001c0003t0039g0116others(1): Show | 4 | HG02056.hp1 HG02273.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+5173_903+5174i others(170): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 130986 | |||||
| chr12:130986
|
ATCCTCAG others(49): Show |
A | 111 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.903+5118_903+5173d others(58): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 130986 | |||||
| chr12:131023
|
T | C | 56 | a0001c0003t0001g0267a0001c0003t0010g0155a0001c0003t0010g0232others(53): Show | 56 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.903+5111T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131023 | ||||||
| chr12:131023
|
T | TCCCCACA others(49): Show |
3 | a0001c0003t0001g0101a0001c0006t0049g0144a0004c0011t0004g0159 | 3 | HG02615.hp1 HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.903+5166_903+5167i others(58): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131023 | |||||
| chr12:131023
|
T | TCCCCACA others(105): Show |
2 | a0004c0008t0053g0199a0018c0054t0014g0279 | 2 | HG01975.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.903+5173_903+5174i others(114): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131023 | |||||
| chr12:131023
|
T | TCCCCACA others(161): Show |
1 | a0002c0001t0016g0121 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.903+5173_903+5174i others(170): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131023 | |||||
| chr12:131023
|
T | TCCCCACA others(217): Show |
4 | a0001c0002t0002g0218a0001c0003t0001g0044a0001c0003t0001g0088others(1): Show | 4 | HG00408.hp1 HG01346.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+5173_903+5174i others(226): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131023 | |||||
| chr12:131033
|
TG | T | 55 | a0001c0003t0001g0267a0001c0003t0010g0155a0001c0003t0010g0232others(52): Show | 55 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.903+5123delG | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131033 | |||||
| chr12:131034
|
G | C | 8 | a0001c0004t0001g0109a0001c0004t0001g0235a0001c0004t0037g0208others(5): Show | 8 | HG02040.hp2 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.903+5122G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131034 | ||||||
| chr12:131035
|
G | C | 63 | a0001c0003t0001g0267a0001c0003t0010g0155a0001c0003t0010g0232others(60): Show | 63 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.903+5123G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131035 | ||||||
| chr12:131036
|
C | CCGCGATC others(45): Show |
7 | a0001c0004t0001g0109a0001c0004t0001g0235a0001c0004t0037g0208others(4): Show | 7 | HG02040.hp2 HG02080.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+5125_903+5126i others(54): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131036 | |||||
| chr12:131036
|
C | CCGCGATC others(213): Show |
1 | a0001c0007t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.903+5125_903+5126i others(222): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131036 | |||||
| chr12:131039
|
C | G | 55 | a0001c0003t0001g0267a0001c0003t0010g0155a0001c0003t0010g0232others(52): Show | 55 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.903+5127C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131039 | ||||||
| chr12:131042
|
C | A | 55 | a0001c0003t0001g0267a0001c0003t0010g0155a0001c0003t0010g0232others(52): Show | 55 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.903+5130C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131042 | ||||||
| chr12:131042
|
C | CGA | 8 | a0001c0004t0001g0109a0001c0004t0001g0235a0001c0004t0037g0208others(5): Show | 8 | HG02040.hp2 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.903+5130_903+5131i others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131042 | ||||||
| chr12:131042
|
C | CTCCTCAG others(48): Show |
6 | a0001c0002t0002g0240a0004c0008t0001g0129a0004c0011t0006g0093others(3): Show | 6 | HG01175.hp1 HG01981.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+5166_903+5167i others(57): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131042 | |||||
| chr12:131042
|
C | CTCCTCAG others(103): Show |
1 | a0001c0006t0002g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.903+5166_903+5167i others(112): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131042 | |||||
| chr12:131042
|
C | CTCCTCAG others(215): Show |
1 | a0003c0010t0019g0178 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.903+5166_903+5167i others(224): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131042 | |||||
| chr12:131042
|
C | CTCCTCAG others(48): Show |
7 | a0001c0002t0002g0114a0001c0002t0002g0127a0001c0002t0002g0205others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.903+5173_903+5174i others(57): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131042 | |||||
| chr12:131042
|
C | CTCCTCAG others(104): Show |
1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.903+5173_903+5174i others(113): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131042 | |||||
| chr12:131042
|
C | CTCCTCAG others(160): Show |
1 | a0001c0003t0004g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.903+5173_903+5174i others(169): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131042 | |||||
| chr12:131042
|
C | CTCCTCAG others(216): Show |
1 | a0002c0001t0002g0143 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.903+5173_903+5174i others(225): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131042 | |||||
| chr12:131042
|
C | CTCCTCAG others(214): Show |
1 | a0001c0006t0002g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.903+5165_903+5166i others(223): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131042 | |||||
| chr12:131099
|
CGCCATCT others(1959): Show |
C | 1 | a0001c0019t0034g0244 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.903+5191_904-5199d others(2): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 131099 | |||||
| chr12:131201
|
C | T | 1 | a0002c0001t0013g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.903+5289C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131201 | ||||||
| chr12:131218
|
T | C | 1 | a0014c0028t0001g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.903+5306T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131218 | ||||||
| chr12:131465
|
C | T | 3 | a0001c0004t0004g0031a0001c0004t0035g0030a0024c0036t0057g0048 | 3 | HG01496.hp1 HG01516.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.903+5553C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131465 | ||||||
| chr12:131475
|
T | C | 51 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.903+5563T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131475 | ||||||
| chr12:131476
|
C | T | 2 | a0001c0043t0004g0063a0002c0015t0046g0224 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.903+5564C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131476 | ||||||
| chr12:131598
|
T | C | 1 | a0003c0017t0002g0089 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.903+5686T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131598 | ||||||
| chr12:131621
|
G | A | 5 | a0003c0005t0002g0252a0003c0005t0062g0073a0005c0013t0001g0250others(2): Show | 5 | HG01167.hp2 HG01952.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+5709G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131621 | ||||||
| chr12:131631
|
C | A | 3 | a0001c0044t0001g0050a0003c0005t0009g0055a0003c0010t0012g0034 | 3 | HG02970.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.903+5719C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131631 | ||||||
| chr12:131697
|
G | A | 47 | a0001c0003t0001g0225a0001c0003t0012g0049a0001c0044t0001g0050others(44): Show | 47 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.903+5785G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131697 | ||||||
| chr12:131770
|
G | A | 1 | a0005c0013t0025g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.903+5858G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131770 | ||||||
| chr12:131879
|
G | A | 4 | a0001c0004t0060g0217a0002c0001t0013g0011a0002c0001t0024g0017others(1): Show | 4 | HG02630.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+5967G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131879 | ||||||
| chr12:131971
|
C | T | 1 | a0003c0005t0003g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.903+6059C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 131971 | ||||||
| chr12:132183
|
G | A | 1 | a0002c0015t0013g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.904-6084G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 132183 | ||||||
| chr12:132281
|
G | A | 2 | a0001c0003t0001g0225a0008c0016t0007g0037 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.904-5986G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 132281 | ||||||
| chr12:132425
|
T | C | 1 | a0020c0047t0042g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.904-5842T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 132425 | ||||||
| chr12:132656
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.904-5611G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 132656 | ||||||
| chr12:132691
|
G | A | 36 | a0001c0002t0002g0039a0001c0002t0002g0123a0001c0002t0002g0167others(33): Show | 36 | HG00408.hp2 HG01106.hp1 HG01981.hp2 others(33): Show |
intron_variant | MODIFIER | c.904-5576G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 132691 | ||||||
| chr12:133064
|
T | C | 224 | a0001c0002t0002g0008a0001c0002t0002g0133a0001c0002t0002g0137others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.904-5203T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 133064 | ||||||
| chr12:133152
|
G | A | 1 | a0003c0045t0045g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.904-5115G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 133152 | ||||||
| chr12:133293
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.904-4974G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 133293 | ||||||
| chr12:133415
|
G | A | 2 | a0002c0001t0006g0097a0002c0001t0006g0151 | 2 | HG00438.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.904-4852G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 133415 | ||||||
| chr12:133461
|
G | C | 2 | a0001c0003t0001g0225a0008c0016t0007g0037 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.904-4806G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 133461 | ||||||
| chr12:133630
|
CAGGTTAG others(92): Show |
C | 2 | a0001c0003t0002g0219a0011c0058t0027g0272 | 2 | NA18942.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.904-4567_904-4469d others(101): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 133630 | |||||
| chr12:133799
|
C | T | 1 | a0002c0009t0002g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.904-4468C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 133799 | ||||||
| chr12:134030
|
T | C | 5 | a0001c0002t0002g0133a0001c0002t0002g0137a0001c0002t0047g0201others(2): Show | 5 | HG01257.hp1 HG02698.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-4237T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134030 | ||||||
| chr12:134118
|
G | A | 2 | a0001c0003t0002g0219a0011c0058t0027g0272 | 2 | NA18942.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.904-4149G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134118 | ||||||
| chr12:134195
|
G | A | 1 | a0004c0011t0004g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.904-4072G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134195 | ||||||
| chr12:134223
|
G | A | 28 | a0001c0002t0002g0167a0001c0002t0048g0105a0001c0003t0002g0060others(25): Show | 28 | HG00408.hp2 HG01106.hp1 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.904-4044G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134223 | ||||||
| chr12:134287
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.904-3980G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134287 | ||||||
| chr12:134371
|
T | C | 1 | a0001c0003t0001g0101 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.904-3896T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134371 | ||||||
| chr12:134654
|
G | A | 28 | a0001c0002t0002g0167a0001c0002t0048g0105a0001c0003t0002g0060others(25): Show | 28 | HG00408.hp2 HG01106.hp1 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.904-3613G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134654 | ||||||
| chr12:134668
|
C | T | 2 | a0008c0016t0007g0058a0008c0016t0061g0015 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.904-3599C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134668 | ||||||
| chr12:134707
|
C | G | 2 | a0001c0002t0002g0261a0011c0058t0027g0272 | 2 | HG00323.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.904-3560C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134707 | ||||||
| chr12:134737
|
A | C | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.904-3530A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134737 | ||||||
| chr12:134775
|
G | A | 4 | a0002c0001t0004g0027a0002c0001t0004g0028a0002c0001t0004g0029others(1): Show | 4 | HG01243.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-3492G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134775 | ||||||
| chr12:134848
|
G | A | 1 | a0003c0005t0025g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.904-3419G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134848 | ||||||
| chr12:134853
|
C | T | 50 | a0001c0002t0047g0201a0001c0003t0001g0044a0001c0003t0001g0086others(47): Show | 50 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.904-3414C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134853 | ||||||
| chr12:134854
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.904-3413G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134854 | ||||||
| chr12:134896
|
T | C | 2 | a0001c0002t0002g0035a0001c0004t0002g0070 | 2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.904-3371T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134896 | ||||||
| chr12:134965
|
T | A | 183 | a0001c0002t0002g0008a0001c0002t0002g0133a0001c0002t0002g0137others(180): Show | 183 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.904-3302T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 134965 | ||||||
| chr12:135023
|
A | G | 115 | a0001c0002t0002g0008a0001c0002t0002g0039a0001c0002t0002g0090others(112): Show | 115 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.904-3244A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135023 | ||||||
| chr12:135045
|
G | A | 2 | a0001c0003t0001g0225a0008c0016t0007g0037 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.904-3222G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135045 | ||||||
| chr12:135061
|
C | T | 48 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(45): Show | 48 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.904-3206C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135061 | ||||||
| chr12:135116
|
C | T | 4 | a0001c0004t0002g0142a0001c0007t0001g0107a0001c0007t0001g0118others(1): Show | 4 | HG02015.hp2 HG02135.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-3151C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135116 | ||||||
| chr12:135146
|
A | G | 1 | a0003c0046t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.904-3121A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135146 | ||||||
| chr12:135321
|
A | G | 1 | a0002c0001t0006g0151 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.904-2946A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135321 | ||||||
| chr12:135360
|
C | T | 3 | a0001c0004t0004g0031a0001c0004t0035g0030a0024c0036t0057g0048 | 3 | HG01496.hp1 HG01516.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.904-2907C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135360 | ||||||
| chr12:135361
|
A | G | 115 | a0001c0002t0002g0008a0001c0002t0002g0167a0001c0002t0048g0105others(112): Show | 115 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.904-2906A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135361 | ||||||
| chr12:135409
|
T | C | 2 | a0008c0016t0007g0058a0008c0016t0061g0015 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.904-2858T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135409 | ||||||
| chr12:135461
|
G | A | 2 | a0001c0003t0002g0219a0011c0058t0027g0272 | 2 | NA18942.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.904-2806G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135461 | ||||||
| chr12:135498
|
C | T | 51 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.904-2769C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135498 | ||||||
| chr12:135702
|
G | T | 5 | a0001c0043t0004g0063a0001c0044t0001g0050a0002c0015t0046g0224others(2): Show | 5 | HG02818.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-2565G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135702 | ||||||
| chr12:135708
|
C | T | 1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.904-2559C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135708 | ||||||
| chr12:135767
|
C | T | 27 | a0001c0002t0002g0167a0001c0002t0048g0105a0001c0003t0002g0060others(24): Show | 27 | HG00408.hp2 HG01106.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.904-2500C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135767 | ||||||
| chr12:135937
|
A | T | 8 | a0001c0002t0002g0008a0001c0003t0002g0219a0002c0001t0013g0011others(5): Show | 8 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.904-2330A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 135937 | ||||||
| chr12:136061
|
C | A | 2 | a0001c0003t0002g0219a0011c0058t0027g0272 | 2 | NA18942.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.904-2206C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 136061 | ||||||
| chr12:136083
|
T | C | 13 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0002g0219others(10): Show | 13 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-2184T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 136083 | ||||||
| chr12:136169
|
T | C | 222 | a0001c0002t0002g0008a0001c0002t0002g0133a0001c0002t0002g0137others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.904-2098T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 136169 | ||||||
| chr12:136256
|
TTGGGAA | T | 43 | a0001c0002t0002g0182a0001c0002t0002g0240a0001c0003t0004g0166others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.904-2006_904-2001d others(8): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 136256 | |||||
| chr12:136262
|
A | G | 1 | a0013c0022t0001g0259 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.904-2005A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 136262 | ||||||
| chr12:136551
|
C | G | 26 | a0001c0002t0048g0105a0001c0003t0002g0060a0001c0003t0002g0102others(23): Show | 26 | HG00408.hp2 HG01106.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.904-1716C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 136551 | ||||||
| chr12:136662
|
A | G | 138 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0099others(135): Show | 139 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.904-1605A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 136662 | ||||||
| chr12:136773
|
C | G | 2 | a0002c0001t0024g0017a0002c0001t0024g0177 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.904-1494C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 136773 | ||||||
| chr12:136792
|
ATTTAAGC others(9): Show |
A | 71 | a0001c0002t0002g0167a0001c0002t0002g0182a0001c0002t0002g0240others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.904-1473_904-1458d others(18): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 136792 | |||||
| chr12:136961
|
C | T | 53 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(50): Show | 53 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.904-1306C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 136961 | ||||||
| chr12:137036
|
G | A | 69 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(66): Show | 69 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.904-1231G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137036 | ||||||
| chr12:137079
|
C | T | 54 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(51): Show | 54 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.904-1188C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137079 | ||||||
| chr12:137089
|
G | C | 2 | a0001c0043t0004g0063a0002c0015t0046g0224 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.904-1178G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137089 | ||||||
| chr12:137178
|
C | T | 1 | a0001c0003t0001g0101 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.904-1089C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137178 | ||||||
| chr12:137248
|
G | A | 2 | a0002c0001t0024g0017a0002c0001t0024g0177 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.904-1019G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137248 | ||||||
| chr12:137302
|
A | AGGGAAGC others(57): Show |
9 | a0002c0001t0001g0019a0002c0001t0001g0191a0002c0001t0008g0020others(6): Show | 9 | HG01074.hp1 HG01358.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-941_904-878dup others(64): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 137302 | |||||
| chr12:137390
|
T | G | 2 | a0001c0003t0001g0225a0008c0016t0007g0037 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.904-877T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137390 | ||||||
| chr12:137603
|
C | G | 1 | a0002c0001t0009g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.904-664C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137603 | ||||||
| chr12:137630
|
TA | T | 11 | a0001c0002t0002g0008a0001c0002t0002g0099a0001c0002t0002g0179others(8): Show | 11 | HG01168.hp1 HG02109.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.904-620delA | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 137630 | |||||
| chr12:137630
|
TAA | T | 71 | a0001c0002t0055g0256a0001c0003t0002g0219a0001c0004t0001g0053others(68): Show | 71 | HG00597.hp1 HG00642.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.904-621_904-620del others(2): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 137630 | |||||
| chr12:137630
|
TAAA | T | 9 | a0001c0004t0003g0082a0001c0006t0002g0104a0001c0037t0011g0194others(6): Show | 9 | HG01167.hp1 HG01517.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-622_904-620del others(3): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 137630 | |||||
| chr12:137825
|
A | AT | 13 | a0001c0002t0002g0099a0001c0007t0001g0122a0002c0001t0001g0202others(10): Show | 13 | HG00280.hp2 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.904-427dupT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 137825 | |||||
| chr12:137882
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.904-385G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137882 | ||||||
| chr12:137959
|
C | T | 4 | a0001c0003t0001g0225a0002c0001t0020g0071a0002c0001t0051g0013others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-308C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 137959 | ||||||
| chr12:138158
|
C | T | 5 | a0001c0043t0004g0063a0002c0001t0001g0010a0002c0001t0024g0017others(2): Show | 5 | HG02630.hp2 HG02818.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-109C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 138158 | ||||||
| chr12:138178
|
A | T | 1 | a0002c0001t0005g0007 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.904-89A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 3/13 | chr12 | 138178 | ||||||
| chr12:139418
|
G | T | 1 | a0001c0006t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1991+64G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 139418 | ||||||
| chr12:139633
|
C | T | 1 | a0002c0001t0022g0038 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1991+279C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 139633 | ||||||
| chr12:139841
|
G | A | 9 | a0002c0001t0001g0202a0002c0001t0050g0051a0002c0009t0002g0080others(6): Show | 9 | HG00280.hp2 HG00741.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1991+487G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 139841 | ||||||
| chr12:139855
|
A | G | 1 | a0009c0020t0001g0238 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1991+501A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 139855 | ||||||
| chr12:139874
|
C | G | 1 | a0021c0032t0001g0108 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1991+520C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 139874 | ||||||
| chr12:140121
|
G | A | 24 | a0001c0043t0004g0063a0002c0001t0024g0017a0002c0001t0024g0177others(21): Show | 24 | HG01981.hp2 HG02080.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1991+767G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140121 | ||||||
| chr12:140206
|
A | G | 2 | a0002c0009t0002g0222a0002c0009t0002g0262 | 2 | HG00735.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1991+852A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140206 | ||||||
| chr12:140367
|
A | C | 1 | a0001c0059t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1992-757A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140367 | ||||||
| chr12:140686
|
G | A | 6 | a0001c0002t0044g0084a0001c0003t0001g0225a0001c0003t0002g0219others(3): Show | 6 | HG02027.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1992-438G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140686 | ||||||
| chr12:140743
|
G | A | 1 | a0003c0010t0019g0178 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1992-381G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140743 | ||||||
| chr12:140776
|
C | G | 103 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(100): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1992-348C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140776 | ||||||
| chr12:140923
|
AT | A | 142 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(139): Show | 143 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1992-200delT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140923 | ||||||
| chr12:140936
|
T | C | 18 | a0001c0002t0002g0001a0004c0008t0001g0129a0004c0008t0001g0173others(15): Show | 19 | HG01981.hp2 HG02027.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1992-188T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140936 | ||||||
| chr12:140962
|
C | A | 13 | a0001c0004t0060g0217a0001c0043t0004g0063a0002c0001t0024g0017others(10): Show | 13 | HG01346.hp2 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1992-162C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140962 | ||||||
| chr12:140964
|
T | C | 178 | a0001c0002t0002g0008a0001c0002t0002g0035a0001c0002t0002g0039others(175): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.1992-160T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 140964 | ||||||
| chr12:141073
|
A | G | 88 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0003t0001g0225others(85): Show | 89 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.1992-51A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 4/13 | chr12 | 141073 | ||||||
| chr12:141412
|
C | T | 64 | a0001c0002t0048g0105a0001c0002t0055g0256a0001c0004t0001g0053others(61): Show | 64 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.2153+127C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 141412 | ||||||
| chr12:141439
|
A | G | 25 | a0001c0002t0002g0001a0001c0002t0044g0084a0001c0003t0001g0126others(22): Show | 26 | HG01175.hp2 HG01346.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.2153+154A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 141439 | ||||||
| chr12:141470
|
G | A | 7 | a0001c0002t0002g0182a0001c0002t0002g0240a0001c0003t0010g0155others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.2153+185G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 141470 | ||||||
| chr12:141821
|
T | C | 129 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(126): Show | 130 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.2153+536T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 141821 | ||||||
| chr12:141864
|
A | T | 1 | a0001c0002t0002g0114 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2153+579A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 141864 | ||||||
| chr12:142126
|
A | G | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2153+841A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142126 | ||||||
| chr12:142166
|
G | C | 13 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(10): Show | 13 | HG01346.hp1 HG01496.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+881G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142166 | ||||||
| chr12:142174
|
C | T | 1 | a0001c0043t0004g0063 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2153+889C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142174 | ||||||
| chr12:142209
|
C | T | 1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2153+924C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142209 | ||||||
| chr12:142257
|
G | C | 3 | a0003c0005t0013g0036a0003c0005t0023g0068a0003c0005t0023g0245 | 3 | HG02615.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2153+972G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142257 | ||||||
| chr12:142390
|
A | G | 1 | a0001c0003t0011g0138 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2153+1105A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142390 | ||||||
| chr12:142496
|
G | A | 3 | a0004c0008t0001g0129a0004c0008t0001g0173a0004c0008t0001g0212 | 3 | HG01981.hp2 HG02080.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2153+1211G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142496 | ||||||
| chr12:142557
|
T | G | 1 | a0002c0001t0003g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2153+1272T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142557 | ||||||
| chr12:142668
|
C | T | 268 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.2153+1383C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 142668 | ||||||
| chr12:143108
|
G | C | 1 | a0003c0005t0003g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2153+1823G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143108 | ||||||
| chr12:143234
|
C | T | 6 | a0001c0004t0060g0217a0002c0001t0024g0017a0002c0001t0024g0177others(3): Show | 6 | HG01167.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+1949C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143234 | ||||||
| chr12:143245
|
T | C | 217 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.2153+1960T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143245 | ||||||
| chr12:143399
|
G | A | 4 | a0001c0003t0001g0225a0002c0001t0009g0064a0006c0012t0004g0065others(1): Show | 4 | HG02622.hp2 HG02897.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2153+2114G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143399 | ||||||
| chr12:143565
|
C | T | 13 | a0002c0001t0001g0019a0002c0001t0001g0191a0002c0001t0008g0020others(10): Show | 13 | HG01074.hp1 HG01358.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+2280C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143565 | ||||||
| chr12:143581
|
AGTTCATG others(53): Show |
A | 4 | a0001c0003t0001g0225a0002c0001t0009g0064a0006c0012t0004g0065others(1): Show | 4 | HG02622.hp2 HG02897.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2153+2326_2153+238 others(64): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143581 | |||||
| chr12:143581
|
AGTTCATG others(83): Show |
A | 1 | a0001c0041t0056g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2153+2326_2153+241 others(94): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143581 | |||||
| chr12:143611
|
AGTTCATG others(23): Show |
A | 213 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2153+2386_2153+241 others(34): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143611 | |||||
| chr12:143619
|
C | T | 3 | a0001c0002t0002g0114a0002c0009t0002g0222a0002c0009t0002g0262 | 3 | HG00735.hp2 HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2153+2334C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143619 | ||||||
| chr12:143642
|
G | A | 1 | a0001c0004t0035g0030 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2153+2357G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143642 | ||||||
| chr12:143671
|
C | G | 189 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.2153+2386C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143671 | ||||||
| chr12:143742
|
G | A | 13 | a0002c0001t0001g0019a0002c0001t0001g0191a0002c0001t0008g0020others(10): Show | 13 | HG01074.hp1 HG01358.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+2457G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143742 | ||||||
| chr12:143780
|
G | A | 1 | a0010c0014t0003g0002 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2153+2495G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143780 | ||||||
| chr12:143826
|
C | CGT | 54 | a0001c0002t0002g0008a0001c0002t0002g0114a0001c0002t0002g0133others(51): Show | 54 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.2153+2581_2153+258 others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143826
|
C | CGTGT | 35 | a0001c0002t0002g0167a0001c0003t0001g0267a0001c0004t0035g0030others(32): Show | 35 | HG00673.hp2 HG01070.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.2153+2579_2153+258 others(8): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143826
|
C | CGTGTGT | 15 | a0001c0002t0002g0182a0001c0002t0002g0240a0001c0003t0004g0166others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.2153+2577_2153+258 others(10): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143826
|
C | CGTGTGTG others(1): Show |
8 | a0002c0001t0004g0029a0002c0001t0008g0026a0002c0015t0046g0224others(5): Show | 8 | HG01358.hp1 HG01884.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.2153+2575_2153+258 others(12): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143826
|
C | CGTGTGTG others(3): Show |
2 | a0003c0005t0023g0245a0009c0020t0001g0238 | 2 | HG01993.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2153+2573_2153+258 others(14): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143826
|
CGT | C | 86 | a0001c0002t0002g0035a0001c0002t0002g0039a0001c0002t0002g0066others(83): Show | 86 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2153+2581_2153+258 others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143826
|
CGTGT | C | 17 | a0001c0003t0002g0169a0001c0003t0010g0155a0001c0003t0010g0232others(14): Show | 17 | HG00280.hp1 HG01074.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2153+2579_2153+258 others(8): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143826
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2153+2573_2153+258 others(14): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143826
|
CGTGTGTG others(5): Show |
C | 3 | a0002c0040t0029g0156a0008c0016t0007g0058a0008c0016t0061g0015 | 3 | HG02145.hp2 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2153+2571_2153+258 others(16): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 143826 | |||||
| chr12:143866
|
T | A | 7 | a0001c0003t0001g0225a0002c0001t0009g0064a0002c0001t0013g0011others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2153+2581T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 143866 | ||||||
| chr12:144010
|
C | G | 1 | a0001c0003t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2153+2725C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 144010 | ||||||
| chr12:144032
|
G | A | 1 | a0002c0001t0013g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2153+2747G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 144032 | ||||||
| chr12:144175
|
C | T | 1 | a0001c0007t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2153+2890C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 144175 | ||||||
| chr12:144256
|
T | G | 201 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2153+2971T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 144256 | ||||||
| chr12:144413
|
G | C | 1 | a0001c0002t0002g0123 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2153+3128G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 144413 | ||||||
| chr12:144630
|
G | C | 5 | a0001c0003t0001g0225a0002c0001t0013g0011a0002c0015t0046g0224others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2153+3345G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 144630 | ||||||
| chr12:144805
|
C | T | 1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2153+3520C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 144805 | ||||||
| chr12:144899
|
A | G | 1 | a0001c0003t0002g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2153+3614A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 144899 | ||||||
| chr12:145215
|
C | T | 57 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(54): Show | 58 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.2153+3930C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 145215 | ||||||
| chr12:145486
|
C | T | 127 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.2153+4201C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 145486 | ||||||
| chr12:145493
|
C | T | 43 | a0001c0004t0001g0091a0001c0004t0001g0109a0001c0004t0001g0170others(40): Show | 43 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.2153+4208C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 145493 | ||||||
| chr12:145502
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2153+4217G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 145502 | ||||||
| chr12:145807
|
A | G | 33 | a0001c0002t0002g0008a0001c0003t0012g0049a0001c0004t0058g0185others(30): Show | 33 | HG00280.hp2 HG00741.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2153+4522A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 145807 | ||||||
| chr12:145961
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2153+4676G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 145961 | ||||||
| chr12:145997
|
C | T | 5 | a0002c0001t0009g0064a0002c0040t0029g0156a0008c0016t0007g0037others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2153+4712C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 145997 | ||||||
| chr12:146003
|
C | T | 1 | a0001c0003t0002g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2153+4718C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146003 | ||||||
| chr12:146029
|
A | C | 126 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2153+4744A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146029 | ||||||
| chr12:146361
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2153+5076G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146361 | ||||||
| chr12:146380
|
C | T | 2 | a0001c0004t0058g0185a0003c0005t0012g0074 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2153+5095C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146380 | ||||||
| chr12:146434
|
C | G | 3 | a0002c0001t0001g0019a0006c0012t0001g0265a0006c0012t0032g0264 | 3 | HG01891.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2153+5149C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146434 | ||||||
| chr12:146469
|
C | T | 2 | a0001c0002t0002g0008a0003c0017t0002g0069 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2153+5184C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146469 | ||||||
| chr12:146473
|
T | C | 1 | a0001c0003t0001g0267 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2153+5188T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146473 | ||||||
| chr12:146486
|
A | T | 1 | a0004c0008t0002g0130 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2153+5201A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146486 | ||||||
| chr12:146487
|
T | A | 8 | a0001c0002t0002g0167a0001c0003t0001g0044a0001c0003t0001g0088others(5): Show | 8 | HG00673.hp1 HG02015.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.2153+5202T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146487 | ||||||
| chr12:146496
|
A | G | 6 | a0001c0004t0060g0217a0002c0001t0024g0017a0002c0001t0024g0177others(3): Show | 6 | HG01167.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+5211A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146496 | ||||||
| chr12:146538
|
C | T | 134 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.2153+5253C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146538 | ||||||
| chr12:146551
|
C | T | 1 | a0004c0011t0004g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2153+5266C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146551 | ||||||
| chr12:146582
|
A | C | 80 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(77): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.2153+5297A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146582 | ||||||
| chr12:146654
|
A | C | 2 | a0001c0004t0058g0185a0003c0005t0012g0074 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2153+5369A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146654 | ||||||
| chr12:146691
|
G | T | 2 | a0001c0004t0058g0185a0003c0005t0012g0074 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2153+5406G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146691 | ||||||
| chr12:146697
|
T | A | 2 | a0001c0004t0058g0185a0003c0005t0012g0074 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2153+5412T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146697 | ||||||
| chr12:146869
|
G | A | 1 | a0001c0004t0035g0030 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2153+5584G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 146869 | ||||||
| chr12:147054
|
T | C | 74 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(71): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.2153+5769T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147054 | ||||||
| chr12:147094
|
T | C | 7 | a0001c0003t0001g0267a0001c0003t0004g0166a0001c0025t0040g0148others(4): Show | 7 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2153+5809T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147094 | ||||||
| chr12:147129
|
G | C | 3 | a0001c0003t0001g0225a0002c0015t0031g0207a0006c0012t0004g0065 | 3 | HG02896.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2153+5844G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147129 | ||||||
| chr12:147187
|
C | T | 2 | a0001c0004t0058g0185a0003c0005t0012g0074 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2153+5902C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147187 | ||||||
| chr12:147211
|
C | T | 3 | a0001c0002t0048g0105a0002c0001t0006g0085a0002c0009t0002g0213 | 3 | HG00438.hp1 HG02165.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2153+5926C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147211 | ||||||
| chr12:147331
|
G | A | 2 | a0001c0002t0002g0035a0001c0002t0002g0066 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2153+6046G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147331 | ||||||
| chr12:147383
|
C | T | 4 | a0001c0004t0058g0185a0003c0005t0012g0074a0005c0018t0001g0248others(1): Show | 4 | HG01167.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2153+6098C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147383 | ||||||
| chr12:147402
|
A | C | 1 | a0004c0008t0052g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2153+6117A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147402 | ||||||
| chr12:147498
|
A | G | 2 | a0001c0003t0001g0225a0006c0012t0004g0065 | 2 | HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2153+6213A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147498 | ||||||
| chr12:147597
|
C | T | 8 | a0002c0001t0001g0191a0002c0001t0008g0020a0002c0001t0008g0023others(5): Show | 8 | HG01074.hp1 HG01358.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2153+6312C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147597 | ||||||
| chr12:147659
|
T | C | 13 | a0001c0002t0002g0182a0001c0002t0002g0240a0001c0019t0001g0139others(10): Show | 13 | HG00099.hp1 HG01070.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+6374T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147659 | ||||||
| chr12:147714
|
C | T | 6 | a0001c0002t0002g0008a0002c0040t0029g0156a0003c0017t0002g0069others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+6429C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147714 | ||||||
| chr12:147894
|
C | T | 87 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(84): Show | 88 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.2153+6609C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147894 | ||||||
| chr12:147898
|
T | G | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2153+6613T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147898 | ||||||
| chr12:147922
|
G | A | 7 | a0002c0001t0001g0202a0008c0035t0007g0135a0009c0020t0001g0211others(4): Show | 7 | HG00280.hp2 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2153+6637G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 147922 | ||||||
| chr12:148000
|
T | C | 2 | a0002c0001t0021g0163a0002c0001t0021g0164 | 2 | HG00621.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2153+6715T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148000 | ||||||
| chr12:148031
|
C | T | 1 | a0001c0003t0001g0204 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2153+6746C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148031 | ||||||
| chr12:148079
|
G | A | 1 | a0002c0015t0031g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2153+6794G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148079 | ||||||
| chr12:148277
|
G | A | 6 | a0001c0002t0002g0008a0002c0040t0029g0156a0003c0017t0002g0069others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+6992G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148277 | ||||||
| chr12:148325
|
G | A | 7 | a0002c0001t0006g0097a0002c0001t0006g0151a0004c0011t0006g0093others(4): Show | 7 | HG00438.hp2 NA18943.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.2153+7040G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148325 | ||||||
| chr12:148345
|
C | G | 79 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(76): Show | 80 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.2153+7060C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148345 | ||||||
| chr12:148429
|
G | C | 4 | a0001c0044t0001g0050a0002c0001t0001g0019a0006c0012t0001g0265others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2153+7144G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148429 | ||||||
| chr12:148467
|
G | T | 73 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(70): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2153+7182G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148467 | ||||||
| chr12:148529
|
T | G | 73 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(70): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2153+7244T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148529 | ||||||
| chr12:148536
|
G | A | 6 | a0001c0002t0002g0008a0002c0040t0029g0156a0003c0017t0002g0069others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+7251G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148536 | ||||||
| chr12:148604
|
C | T | 3 | a0001c0003t0012g0049a0002c0001t0001g0010a0003c0010t0012g0034 | 3 | HG02055.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2153+7319C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148604 | ||||||
| chr12:148610
|
G | A | 6 | a0001c0007t0001g0117a0002c0015t0013g0018a0003c0005t0013g0036others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+7325G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148610 | ||||||
| chr12:148770
|
A | C | 271 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2153+7485A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148770 | ||||||
| chr12:148821
|
C | T | 41 | a0001c0003t0001g0225a0001c0004t0001g0091a0001c0004t0001g0109others(38): Show | 41 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.2153+7536C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 148821 | ||||||
| chr12:149036
|
C | T | 1 | a0005c0018t0008g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2153+7751C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149036 | ||||||
| chr12:149075
|
G | A | 1 | a0001c0003t0007g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2153+7790G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149075 | ||||||
| chr12:149180
|
T | G | 77 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2154-7845T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149180 | ||||||
| chr12:149190
|
G | A | 5 | a0002c0015t0013g0018a0003c0005t0013g0036a0003c0005t0023g0068others(2): Show | 5 | HG01167.hp1 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154-7835G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149190 | ||||||
| chr12:149197
|
C | T | 6 | a0001c0002t0002g0008a0002c0040t0029g0156a0003c0017t0002g0069others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-7828C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149197 | ||||||
| chr12:149199
|
C | T | 6 | a0001c0002t0002g0008a0002c0040t0029g0156a0003c0017t0002g0069others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-7826C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149199 | ||||||
| chr12:149213
|
C | G | 77 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2154-7812C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149213 | ||||||
| chr12:149215
|
G | A | 77 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2154-7810G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149215 | ||||||
| chr12:149252
|
G | C | 77 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2154-7773G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149252 | ||||||
| chr12:149419
|
A | G | 76 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(73): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2154-7606A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149419 | ||||||
| chr12:149441
|
G | C | 82 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.2154-7584G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149441 | ||||||
| chr12:149512
|
C | G | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2154-7513C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149512 | ||||||
| chr12:149513
|
G | A | 2 | a0001c0002t0047g0201a0001c0003t0001g0204 | 2 | HG01257.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2154-7512G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149513 | ||||||
| chr12:149531
|
G | T | 1 | a0001c0003t0002g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2154-7494G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149531 | ||||||
| chr12:149572
|
G | T | 1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2154-7453G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149572 | ||||||
| chr12:149580
|
G | A | 1 | a0003c0017t0015g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2154-7445G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149580 | ||||||
| chr12:149635
|
G | A | 5 | a0001c0004t0060g0217a0002c0001t0024g0017a0002c0001t0024g0177others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-7390G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149635 | ||||||
| chr12:149641
|
T | C | 82 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.2154-7384T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149641 | ||||||
| chr12:149844
|
G | C | 1 | a0001c0003t0002g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2154-7181G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149844 | ||||||
| chr12:149981
|
C | T | 1 | a0001c0033t0013g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2154-7044C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149981 | ||||||
| chr12:149985
|
G | C | 1 | a0001c0007t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2154-7040G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 149985 | ||||||
| chr12:150039
|
G | A | 7 | a0001c0003t0001g0267a0001c0003t0004g0166a0001c0025t0040g0148others(4): Show | 7 | HG00673.hp2 HG00733.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154-6986G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150039 | ||||||
| chr12:150075
|
G | C | 77 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2154-6950G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150075 | ||||||
| chr12:150099
|
T | G | 1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2154-6926T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150099 | ||||||
| chr12:150134
|
G | A | 1 | a0001c0004t0058g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2154-6891G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150134 | ||||||
| chr12:150190
|
G | A | 1 | a0005c0031t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2154-6835G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150190 | ||||||
| chr12:150280
|
C | G | 5 | a0001c0004t0002g0070a0001c0004t0012g0021a0001c0004t0012g0022others(2): Show | 5 | HG01081.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-6745C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150280 | ||||||
| chr12:150462
|
A | T | 1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2154-6563A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150462 | ||||||
| chr12:150498
|
G | T | 77 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2154-6527G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150498 | ||||||
| chr12:150649
|
G | A | 1 | a0002c0001t0003g0216 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2154-6376G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150649 | ||||||
| chr12:150664
|
A | G | 1 | a0002c0009t0002g0262 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2154-6361A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150664 | ||||||
| chr12:150726
|
G | A | 1 | a0011c0055t0018g0271 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2154-6299G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150726 | ||||||
| chr12:150917
|
C | T | 1 | a0002c0001t0005g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2154-6108C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150917 | ||||||
| chr12:150992
|
A | T | 5 | a0002c0015t0013g0018a0003c0005t0013g0036a0003c0005t0023g0068others(2): Show | 5 | HG01167.hp1 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154-6033A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 150992 | ||||||
| chr12:151048
|
A | G | 228 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.2154-5977A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151048 | ||||||
| chr12:151049
|
C | T | 228 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.2154-5976C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151049 | ||||||
| chr12:151075
|
AACTTCGT others(150): Show |
A | 88 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(85): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2154-5872_2154-571 others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 151075 | |||||
| chr12:151084
|
T | C | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2154-5941T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151084 | ||||||
| chr12:151205
|
A | G | 2 | a0002c0009t0002g0080a0002c0009t0002g0081 | 2 | HG02273.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2154-5820A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151205 | ||||||
| chr12:151206
|
C | CGGTAGCT others(150): Show |
4 | a0002c0001t0001g0202a0009c0020t0001g0211a0009c0051t0001g0242others(1): Show | 4 | HG00741.hp1 HG01070.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-5794_2154-579 others(161): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 151206 | |||||
| chr12:151206
|
C | T | 2 | a0002c0009t0002g0080a0002c0009t0002g0081 | 2 | HG02273.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2154-5819C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151206 | ||||||
| chr12:151232
|
G | A | 127 | a0001c0002t0002g0182a0001c0002t0002g0240a0001c0003t0001g0267others(124): Show | 127 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.2154-5793G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151232 | ||||||
| chr12:151275
|
G | A | 1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2154-5750G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151275 | ||||||
| chr12:151404
|
G | A | 1 | a0001c0003t0002g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2154-5621G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151404 | ||||||
| chr12:151500
|
G | A | 1 | a0001c0003t0002g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2154-5525G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151500 | ||||||
| chr12:151516
|
T | C | 51 | a0001c0002t0002g0182a0001c0002t0002g0240a0001c0003t0001g0267others(48): Show | 51 | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.2154-5509T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151516 | ||||||
| chr12:151527
|
C | T | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2154-5498C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151527 | ||||||
| chr12:151566
|
T | A | 1 | a0001c0002t0002g0001 | 2 | HG02027.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2154-5459T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151566 | ||||||
| chr12:151573
|
T | C | 8 | a0001c0002t0002g0008a0001c0004t0058g0185a0002c0040t0029g0156others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2154-5452T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151573 | ||||||
| chr12:151704
|
G | A | 42 | a0001c0003t0001g0225a0001c0004t0001g0091a0001c0004t0001g0109others(39): Show | 42 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.2154-5321G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151704 | ||||||
| chr12:151868
|
C | G | 41 | a0001c0002t0002g0182a0001c0002t0002g0240a0001c0004t0003g0082others(38): Show | 41 | HG00099.hp1 HG00597.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.2154-5157C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151868 | ||||||
| chr12:151920
|
T | A | 48 | a0001c0003t0001g0225a0001c0003t0012g0049a0001c0004t0001g0091others(45): Show | 48 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.2154-5105T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151920 | ||||||
| chr12:151997
|
C | G | 1 | a0024c0036t0057g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2154-5028C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 151997 | ||||||
| chr12:152005
|
T | C | 1 | a0004c0008t0001g0173 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2154-5020T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152005 | ||||||
| chr12:152067
|
G | A | 2 | a0002c0001t0005g0007a0003c0017t0015g0056 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2154-4958G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152067 | ||||||
| chr12:152130
|
G | A | 3 | a0001c0003t0012g0049a0002c0001t0001g0010a0003c0010t0012g0034 | 3 | HG02055.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2154-4895G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152130 | ||||||
| chr12:152273
|
C | T | 1 | a0019c0052t0014g0278 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2154-4752C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152273 | ||||||
| chr12:152491
|
G | T | 3 | a0003c0005t0013g0036a0003c0005t0023g0068a0003c0005t0023g0245 | 3 | HG02615.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2154-4534G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152491 | ||||||
| chr12:152510
|
C | A | 142 | a0001c0002t0002g0008a0001c0002t0002g0182a0001c0002t0002g0240others(139): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.2154-4515C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152510 | ||||||
| chr12:152607
|
T | C | 1 | a0002c0001t0006g0097 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2154-4418T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152607 | ||||||
| chr12:152609
|
A | T | 1 | a0008c0016t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2154-4416A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152609 | ||||||
| chr12:152618
|
A | G | 225 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2154-4407A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152618 | ||||||
| chr12:152658
|
A | G | 82 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(79): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.2154-4367A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152658 | ||||||
| chr12:152672
|
C | T | 3 | a0003c0010t0002g0203a0013c0022t0001g0237a0013c0022t0001g0259 | 3 | HG00099.hp2 HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2154-4353C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152672 | ||||||
| chr12:152673
|
G | A | 3 | a0001c0002t0002g0035a0001c0002t0002g0066a0002c0001t0051g0013 | 3 | HG01884.hp1 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2154-4352G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152673 | ||||||
| chr12:152731
|
G | T | 1 | a0001c0002t0002g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2154-4294G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152731 | ||||||
| chr12:152763
|
T | C | 81 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(78): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.2154-4262T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152763 | ||||||
| chr12:152875
|
G | A | 43 | a0001c0003t0001g0225a0001c0004t0001g0091a0001c0004t0001g0109others(40): Show | 43 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.2154-4150G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 152875 | ||||||
| chr12:153144
|
A | C | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2154-3881A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153144 | ||||||
| chr12:153230
|
G | A | 7 | a0002c0001t0001g0191a0002c0001t0008g0020a0002c0001t0008g0023others(4): Show | 7 | HG01074.hp1 HG01358.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154-3795G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153230 | ||||||
| chr12:153325
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2154-3700G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153325 | ||||||
| chr12:153349
|
G | C | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2154-3676G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153349 | ||||||
| chr12:153414
|
C | T | 1 | a0003c0005t0012g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2154-3611C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153414 | ||||||
| chr12:153480
|
C | G | 232 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2154-3545C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153480 | ||||||
| chr12:153498
|
G | A | 1 | a0003c0005t0028g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2154-3527G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153498 | ||||||
| chr12:153686
|
G | T | 1 | a0004c0008t0052g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2154-3339G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153686 | ||||||
| chr12:153850
|
A | G | 1 | a0001c0004t0001g0235 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2154-3175A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153850 | ||||||
| chr12:153871
|
A | G | 1 | a0001c0003t0011g0138 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2154-3154A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153871 | ||||||
| chr12:153914
|
A | G | 1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2154-3111A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153914 | ||||||
| chr12:153917
|
A | C | 271 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2154-3108A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153917 | ||||||
| chr12:153922
|
C | T | 1 | a0009c0051t0001g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2154-3103C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153922 | ||||||
| chr12:153979
|
C | A | 4 | a0001c0003t0012g0049a0002c0001t0001g0010a0003c0010t0012g0034others(1): Show | 4 | HG02055.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-3046C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 153979 | ||||||
| chr12:154060
|
G | C | 1 | a0001c0037t0011g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2154-2965G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154060 | ||||||
| chr12:154103
|
C | T | 1 | a0004c0011t0004g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2154-2922C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154103 | ||||||
| chr12:154160
|
C | T | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2154-2865C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154160 | ||||||
| chr12:154162
|
A | T | 6 | a0001c0002t0002g0008a0002c0040t0029g0156a0003c0017t0002g0069others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-2863A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154162 | ||||||
| chr12:154199
|
C | T | 2 | a0001c0002t0002g0008a0003c0017t0002g0069 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2154-2826C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154199 | ||||||
| chr12:154302
|
A | T | 91 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(88): Show | 91 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2154-2723A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154302 | ||||||
| chr12:154305
|
AGCT | A | 216 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.2154-2716_2154-271 others(7): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 154305 | |||||
| chr12:154314
|
C | T | 2 | a0003c0010t0019g0178a0005c0013t0001g0250 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2154-2711C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154314 | ||||||
| chr12:154342
|
A | G | 36 | a0001c0003t0001g0225a0001c0003t0001g0267a0001c0003t0002g0219others(33): Show | 36 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.2154-2683A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154342 | ||||||
| chr12:154364
|
C | T | 34 | a0001c0003t0001g0225a0001c0003t0001g0267a0001c0003t0002g0219others(31): Show | 34 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2154-2661C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154364 | ||||||
| chr12:154404
|
G | T | 5 | a0001c0002t0048g0105a0001c0006t0002g0092a0001c0006t0002g0154others(2): Show | 5 | HG02071.hp1 HG02129.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154-2621G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154404 | ||||||
| chr12:154539
|
G | C | 35 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(32): Show | 35 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2154-2486G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154539 | ||||||
| chr12:154630
|
G | T | 29 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(26): Show | 29 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2154-2395G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154630 | ||||||
| chr12:154668
|
C | T | 8 | a0001c0033t0013g0147a0002c0015t0013g0018a0002c0015t0046g0224others(5): Show | 8 | HG01167.hp1 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2154-2357C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154668 | ||||||
| chr12:154669
|
G | A | 1 | a0001c0003t0001g0225 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2154-2356G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154669 | ||||||
| chr12:154673
|
T | C | 53 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(50): Show | 53 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.2154-2352T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154673 | ||||||
| chr12:154696
|
C | T | 8 | a0001c0002t0002g0008a0001c0003t0001g0225a0002c0040t0029g0156others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2154-2329C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154696 | ||||||
| chr12:154788
|
T | C | 194 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2154-2237T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154788 | ||||||
| chr12:154820
|
T | C | 100 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(97): Show | 100 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.2154-2205T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154820 | ||||||
| chr12:154830
|
C | G | 194 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2154-2195C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154830 | ||||||
| chr12:154840
|
CCT | C | 48 | a0001c0003t0002g0219a0001c0004t0001g0091a0001c0004t0001g0109others(45): Show | 48 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.2154-2184_2154-218 others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154840 | ||||||
| chr12:154891
|
G | A | 1 | a0001c0006t0002g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2154-2134G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154891 | ||||||
| chr12:154907
|
G | C | 1 | a0003c0005t0013g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2154-2118G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154907 | ||||||
| chr12:154950
|
AC | A | 77 | a0001c0004t0001g0091a0001c0004t0001g0109a0001c0004t0001g0170others(74): Show | 77 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.2154-2070delC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 154950 | |||||
| chr12:154967
|
C | A | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2154-2058C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154967 | ||||||
| chr12:154970
|
T | C | 97 | a0001c0002t0002g0008a0001c0002t0002g0098a0001c0002t0002g0127others(94): Show | 97 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.2154-2055T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154970 | ||||||
| chr12:154971
|
G | A | 2 | a0001c0002t0002g0008a0003c0017t0002g0069 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2154-2054G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154971 | ||||||
| chr12:154974
|
G | A | 1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2154-2051G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 154974 | ||||||
| chr12:155022
|
T | C | 50 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(47): Show | 50 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.2154-2003T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155022 | ||||||
| chr12:155099
|
G | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2154-1926G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155099 | ||||||
| chr12:155139
|
G | A | 37 | a0001c0004t0001g0091a0001c0004t0001g0109a0001c0004t0001g0235others(34): Show | 37 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.2154-1886G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155139 | ||||||
| chr12:155177
|
C | T | 24 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(21): Show | 24 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2154-1848C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155177 | ||||||
| chr12:155197
|
C | T | 1 | a0001c0002t0002g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2154-1828C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155197 | ||||||
| chr12:155239
|
T | G | 272 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.2154-1786T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155239 | ||||||
| chr12:155315
|
C | A | 1 | a0009c0051t0001g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2154-1710C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155315 | ||||||
| chr12:155421
|
C | T | 1 | a0001c0002t0002g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2154-1604C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155421 | ||||||
| chr12:155432
|
C | T | 10 | a0001c0004t0001g0109a0001c0004t0001g0235a0001c0004t0037g0208others(7): Show | 10 | HG00597.hp1 HG00621.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.2154-1593C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155432 | ||||||
| chr12:155458
|
C | T | 22 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(19): Show | 22 | HG01243.hp1 HG01346.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.2154-1567C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155458 | ||||||
| chr12:155498
|
C | T | 3 | a0008c0035t0007g0135a0022c0038t0007g0255a0023c0039t0030g0094 | 3 | HG00280.hp2 HG01358.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2154-1527C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155498 | ||||||
| chr12:155522
|
C | T | 80 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(77): Show | 80 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.2154-1503C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155522 | ||||||
| chr12:155586
|
C | T | 1 | a0001c0003t0001g0086 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2154-1439C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155586 | ||||||
| chr12:155624
|
T | C | 1 | a0002c0040t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2154-1401T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155624 | ||||||
| chr12:155658
|
G | A | 1 | a0003c0005t0059g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2154-1367G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155658 | ||||||
| chr12:155693
|
C | T | 3 | a0001c0004t0003g0082a0002c0001t0003g0215a0020c0047t0042g0236 | 3 | HG01517.hp1 HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2154-1332C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155693 | ||||||
| chr12:155749
|
G | A | 3 | a0001c0003t0002g0060a0001c0003t0002g0102a0001c0003t0002g0187 | 3 | HG02155.hp2 NA18963.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2154-1276G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155749 | ||||||
| chr12:155917
|
C | T | 73 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(70): Show | 73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2154-1108C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 155917 | ||||||
| chr12:156119
|
G | C | 1 | a0003c0005t0013g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2154-906G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156119 | ||||||
| chr12:156144
|
A | T | 23 | a0001c0004t0003g0082a0001c0004t0058g0185a0001c0041t0056g0072others(20): Show | 23 | HG00597.hp2 HG00735.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.2154-881A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156144 | ||||||
| chr12:156241
|
AAGGCCCT others(17): Show |
A | 1 | a0005c0018t0001g0248 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2154-781_2154-758d others(26): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 156241 | |||||
| chr12:156338
|
C | T | 1 | a0002c0001t0016g0121 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2154-687C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156338 | ||||||
| chr12:156351
|
A | G | 85 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(82): Show | 85 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.2154-674A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156351 | ||||||
| chr12:156364
|
A | G | 81 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(78): Show | 81 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.2154-661A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156364 | ||||||
| chr12:156449
|
G | GGCTGGGG others(31): Show |
1 | a0002c0001t0009g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2154-550_2154-513d others(40): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 156449 | |||||
| chr12:156635
|
G | A | 10 | a0001c0002t0002g0008a0001c0033t0013g0147a0002c0015t0013g0018others(7): Show | 10 | HG01167.hp1 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2154-390G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156635 | ||||||
| chr12:156704
|
C | T | 4 | a0001c0003t0002g0219a0002c0001t0013g0011a0002c0001t0020g0071others(1): Show | 4 | HG02451.hp2 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-321C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156704 | ||||||
| chr12:156771
|
C | T | 1 | a0001c0006t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2154-254C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156771 | ||||||
| chr12:156789
|
A | C | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2154-236A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156789 | ||||||
| chr12:156855
|
T | A | 1 | a0001c0006t0002g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2154-170T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156855 | ||||||
| chr12:156892
|
A | C | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2154-133A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156892 | ||||||
| chr12:156921
|
G | A | 1 | a0001c0004t0058g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2154-104G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 5/13 | chr12 | 156921 | ||||||
| chr12:157211
|
A | C | 3 | a0002c0001t0013g0011a0002c0001t0020g0071a0002c0001t0051g0013 | 3 | HG02451.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2276+64A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 6/13 | chr12 | 157211 | ||||||
| chr12:157305
|
G | C | 3 | a0002c0001t0013g0011a0002c0001t0020g0071a0002c0001t0051g0013 | 3 | HG02451.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2276+158G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 6/13 | chr12 | 157305 | ||||||
| chr12:157334
|
G | A | 2 | a0001c0003t0002g0219a0001c0004t0035g0030 | 2 | HG01516.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.2276+187G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 6/13 | chr12 | 157334 | ||||||
| chr12:157499
|
C | T | 9 | a0001c0033t0013g0147a0002c0001t0008g0020a0002c0015t0013g0018others(6): Show | 9 | HG01074.hp1 HG01167.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2277-29C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 6/13 | chr12 | 157499 | ||||||
| chr12:157523
|
C | G | 1 | a0001c0019t0001g0139 | 1 | HG01070.hp2 | splice_region_variant&intron_variant | LOW | c.2277-5C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 6/13 | chr12 | 157523 | ||||||
| chr12:157745
|
C | T | 1 | a0003c0017t0015g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2443+51C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157745 | ||||||
| chr12:157758
|
G | A | 3 | a0001c0004t0003g0082a0002c0001t0003g0215a0020c0047t0042g0236 | 3 | HG01517.hp1 HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2443+64G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157758 | ||||||
| chr12:157767
|
G | A | 1 | a0001c0004t0058g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2443+73G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157767 | ||||||
| chr12:157808
|
G | C | 1 | a0001c0006t0049g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2443+114G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157808 | ||||||
| chr12:157848
|
G | C | 1 | a0002c0001t0003g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2443+154G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157848 | ||||||
| chr12:157874
|
T | G | 11 | a0001c0003t0012g0049a0002c0001t0001g0010a0002c0001t0001g0191others(8): Show | 11 | HG01074.hp1 HG01358.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2443+180T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157874 | ||||||
| chr12:157893
|
C | T | 23 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(20): Show | 23 | HG00673.hp2 HG00733.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2443+199C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157893 | ||||||
| chr12:157913
|
G | A | 3 | a0002c0015t0031g0207a0003c0005t0025g0024a0005c0013t0025g0115 | 3 | HG02257.hp2 HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2443+219G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157913 | ||||||
| chr12:157949
|
G | A | 1 | a0003c0005t0009g0281 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2443+255G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157949 | ||||||
| chr12:157982
|
C | T | 1 | a0001c0002t0044g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2443+288C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 157982 | ||||||
| chr12:158053
|
A | T | 3 | a0008c0035t0007g0135a0022c0038t0007g0255a0023c0039t0030g0094 | 3 | HG00280.hp2 HG01358.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2443+359A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158053 | ||||||
| chr12:158071
|
G | A | 4 | a0001c0004t0003g0082a0001c0004t0058g0185a0002c0001t0003g0215others(1): Show | 4 | HG01517.hp1 HG02630.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2443+377G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158071 | ||||||
| chr12:158077
|
T | C | 4 | a0001c0004t0003g0082a0001c0004t0058g0185a0002c0001t0003g0215others(1): Show | 4 | HG01517.hp1 HG02630.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2443+383T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158077 | ||||||
| chr12:158343
|
T | C | 38 | a0001c0003t0001g0267a0001c0003t0004g0166a0001c0004t0060g0217others(35): Show | 38 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.2443+649T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158343 | ||||||
| chr12:158434
|
G | A | 1 | a0001c0007t0001g0153 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2443+740G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158434 | ||||||
| chr12:158544
|
G | A | 55 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(52): Show | 55 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2443+850G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158544 | ||||||
| chr12:158549
|
C | T | 38 | a0001c0003t0001g0267a0001c0003t0004g0166a0001c0004t0060g0217others(35): Show | 38 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.2443+855C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158549 | ||||||
| chr12:158564
|
A | T | 6 | a0001c0002t0002g0008a0002c0040t0029g0156a0003c0017t0002g0069others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2443+870A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158564 | ||||||
| chr12:158598
|
T | C | 44 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(41): Show | 44 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.2443+904T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158598 | ||||||
| chr12:158599
|
G | A | 44 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(41): Show | 44 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.2443+905G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158599 | ||||||
| chr12:158626
|
A | G | 55 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(52): Show | 55 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2443+932A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158626 | ||||||
| chr12:158680
|
T | C | 44 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(41): Show | 44 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.2443+986T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158680 | ||||||
| chr12:158704
|
G | C | 90 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(87): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2443+1010G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158704 | ||||||
| chr12:158723
|
G | A | 145 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2443+1029G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158723 | ||||||
| chr12:158746
|
C | A | 1 | a0001c0006t0002g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2443+1052C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158746 | ||||||
| chr12:158770
|
T | C | 10 | a0001c0002t0002g0001a0001c0002t0002g0099a0001c0002t0002g0100others(7): Show | 11 | HG01943.hp2 HG01975.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.2443+1076T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158770 | ||||||
| chr12:158770
|
T | G | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2443+1076T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158770 | ||||||
| chr12:158791
|
C | T | 55 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(52): Show | 55 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2443+1097C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158791 | ||||||
| chr12:158838
|
T | A | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2443+1144T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158838 | ||||||
| chr12:158848
|
G | A | 4 | a0001c0004t0003g0082a0001c0004t0058g0185a0002c0001t0003g0215others(1): Show | 4 | HG01517.hp1 HG02630.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2443+1154G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158848 | ||||||
| chr12:158870
|
A | G | 55 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(52): Show | 55 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2443+1176A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158870 | ||||||
| chr12:158902
|
G | A | 6 | a0001c0002t0002g0008a0002c0040t0029g0156a0003c0017t0002g0069others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2443+1208G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158902 | ||||||
| chr12:158986
|
G | T | 11 | a0001c0003t0012g0049a0002c0001t0001g0010a0002c0001t0001g0191others(8): Show | 11 | HG01074.hp1 HG01358.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2443+1292G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158986 | ||||||
| chr12:158989
|
C | T | 44 | a0001c0002t0002g0008a0001c0003t0001g0267a0001c0003t0004g0166others(41): Show | 44 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.2443+1295C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 158989 | ||||||
| chr12:159053
|
C | A | 1 | a0001c0004t0058g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2443+1359C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159053 | ||||||
| chr12:159188
|
C | T | 88 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(85): Show | 88 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.2443+1494C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159188 | ||||||
| chr12:159233
|
G | A | 86 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(83): Show | 87 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.2443+1539G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159233 | ||||||
| chr12:159233
|
G | T | 1 | a0001c0004t0058g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2443+1539G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159233 | ||||||
| chr12:159253
|
T | C | 175 | a0001c0002t0002g0008a0001c0003t0001g0044a0001c0003t0001g0086others(172): Show | 175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2443+1559T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159253 | ||||||
| chr12:159328
|
T | C | 3 | a0001c0003t0012g0049a0002c0001t0001g0010a0003c0010t0012g0034 | 3 | HG02055.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2443+1634T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159328 | ||||||
| chr12:159379
|
C | T | 3 | a0001c0003t0012g0049a0002c0001t0001g0010a0003c0010t0012g0034 | 3 | HG02055.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2443+1685C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159379 | ||||||
| chr12:159380
|
AGATTCCT others(41): Show |
A | 1 | a0001c0002t0002g0239 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2443+1687_2443+173 others(52): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159380 | ||||||
| chr12:159396
|
C | A | 2 | a0002c0001t0020g0071a0002c0001t0051g0013 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2443+1702C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159396 | ||||||
| chr12:159428
|
T | C | 94 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(91): Show | 94 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.2443+1734T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159428 | ||||||
| chr12:159459
|
T | A | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2443+1765T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159459 | ||||||
| chr12:159936
|
T | TTTCTGGA others(25): Show |
1 | a0007c0021t0004g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2444-1988_2444-195 others(36): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 159936 | |||||
| chr12:159978
|
C | T | 80 | a0001c0002t0002g0008a0001c0003t0001g0044a0001c0003t0001g0086others(77): Show | 80 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.2444-1948C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 159978 | ||||||
| chr12:160009
|
C | T | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2444-1917C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160009 | ||||||
| chr12:160010
|
A | C | 1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2444-1916A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160010 | ||||||
| chr12:160098
|
C | T | 2 | a0001c0003t0010g0155a0001c0003t0010g0232 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2444-1828C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160098 | ||||||
| chr12:160176
|
GT | G | 131 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(128): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.2444-1740delT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 160176 | |||||
| chr12:160176
|
GTT | G | 39 | a0001c0002t0002g0008a0001c0004t0001g0091a0001c0004t0001g0109others(36): Show | 39 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2444-1741_2444-174 others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 160176 | |||||
| chr12:160185
|
T | C | 1 | a0001c0007t0001g0122 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2444-1741T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160185 | ||||||
| chr12:160186
|
T | C | 95 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(92): Show | 95 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.2444-1740T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160186 | ||||||
| chr12:160250
|
T | C | 3 | a0001c0003t0002g0219a0001c0003t0010g0155a0001c0003t0010g0232 | 3 | HG00280.hp1 HG01074.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.2444-1676T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160250 | ||||||
| chr12:160365
|
C | T | 93 | a0001c0002t0002g0001a0001c0002t0002g0035a0001c0002t0002g0039others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2444-1561C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160365 | ||||||
| chr12:160556
|
C | T | 62 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(59): Show | 62 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.2444-1370C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160556 | ||||||
| chr12:160557
|
G | A | 92 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(89): Show | 92 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.2444-1369G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160557 | ||||||
| chr12:160662
|
C | T | 1 | a0001c0003t0002g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2444-1264C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160662 | ||||||
| chr12:160740
|
C | T | 1 | a0007c0050t0010g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2444-1186C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160740 | ||||||
| chr12:160785
|
T | C | 73 | a0001c0002t0002g0008a0001c0003t0001g0225a0001c0003t0001g0267others(70): Show | 73 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.2444-1141T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160785 | ||||||
| chr12:160853
|
G | T | 4 | a0001c0004t0060g0217a0002c0001t0024g0017a0002c0001t0024g0177others(1): Show | 4 | HG02630.hp2 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2444-1073G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160853 | ||||||
| chr12:160880
|
T | C | 2 | a0003c0005t0009g0009a0003c0005t0009g0055 | 2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2444-1046T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160880 | ||||||
| chr12:160938
|
G | A | 108 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(105): Show | 108 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2444-988G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160938 | ||||||
| chr12:160994
|
G | T | 1 | a0001c0004t0058g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2444-932G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 160994 | ||||||
| chr12:161063
|
G | A | 167 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(164): Show | 167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.2444-863G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161063 | ||||||
| chr12:161113
|
G | A | 1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2444-813G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161113 | ||||||
| chr12:161394
|
G | T | 1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2444-532G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161394 | ||||||
| chr12:161516
|
C | T | 232 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2444-410C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161516 | ||||||
| chr12:161603
|
C | T | 2 | a0001c0004t0058g0185a0003c0010t0020g0078 | 2 | HG01884.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2444-323C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161603 | ||||||
| chr12:161607
|
C | G | 177 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(174): Show | 178 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2444-319C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161607 | ||||||
| chr12:161639
|
C | T | 92 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(89): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.2444-287C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161639 | ||||||
| chr12:161667
|
C | T | 5 | a0001c0003t0001g0045a0001c0003t0001g0113a0001c0003t0001g0157others(2): Show | 5 | HG01943.hp2 HG01975.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2444-259C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161667 | ||||||
| chr12:161730
|
A | G | 63 | a0001c0003t0001g0267a0001c0004t0001g0091a0001c0004t0001g0170others(60): Show | 63 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.2444-196A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161730 | ||||||
| chr12:161751
|
A | C | 1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2444-175A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161751 | ||||||
| chr12:161824
|
C | T | 1 | a0001c0002t0002g0039 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2444-102C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161824 | ||||||
| chr12:161856
|
G | A | 240 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.2444-70G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 7/13 | chr12 | 161856 | ||||||
| chr12:162206
|
C | T | 1 | a0001c0007t0001g0103 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2583+141C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162206 | ||||||
| chr12:162207
|
A | G | 262 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2583+142A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162207 | ||||||
| chr12:162220
|
CT | C | 153 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(150): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2583+166delT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 162220 | |||||
| chr12:162246
|
T | C | 2 | a0001c0003t0010g0155a0001c0003t0010g0232 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2583+181T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162246 | ||||||
| chr12:162411
|
G | T | 1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2583+346G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162411 | ||||||
| chr12:162412
|
T | G | 1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2583+347T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162412 | ||||||
| chr12:162453
|
A | T | 2 | a0001c0003t0010g0155a0001c0003t0010g0232 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2583+388A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162453 | ||||||
| chr12:162453
|
ATCAC | A | 7 | a0008c0016t0007g0037a0008c0016t0007g0058a0008c0016t0061g0015others(4): Show | 7 | HG00280.hp2 HG00733.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.2583+389_2583+392d others(6): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162453 | ||||||
| chr12:162459
|
A | C | 7 | a0008c0016t0007g0037a0008c0016t0007g0058a0008c0016t0061g0015others(4): Show | 7 | HG00280.hp2 HG00733.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.2583+394A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162459 | ||||||
| chr12:162461
|
A | G | 7 | a0008c0016t0007g0037a0008c0016t0007g0058a0008c0016t0061g0015others(4): Show | 7 | HG00280.hp2 HG00733.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.2583+396A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162461 | ||||||
| chr12:162618
|
A | C | 2 | a0003c0005t0009g0009a0003c0005t0009g0055 | 2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2583+553A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162618 | ||||||
| chr12:162640
|
T | C | 246 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2583+575T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162640 | ||||||
| chr12:162833
|
T | G | 88 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(85): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2584-661T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162833 | ||||||
| chr12:162879
|
G | A | 1 | a0001c0042t0001g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2584-615G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162879 | ||||||
| chr12:162899
|
G | A | 1 | a0004c0008t0052g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2584-595G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162899 | ||||||
| chr12:162900
|
A | G | 1 | a0001c0004t0012g0021 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2584-594A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162900 | ||||||
| chr12:162933
|
A | G | 8 | a0001c0003t0002g0219a0001c0003t0010g0155a0001c0003t0010g0232others(5): Show | 8 | HG00280.hp1 HG01074.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2584-561A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 162933 | ||||||
| chr12:163063
|
A | G | 88 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(85): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2584-431A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163063 | ||||||
| chr12:163114
|
T | C | 1 | a0010c0014t0001g0076 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2584-380T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163114 | ||||||
| chr12:163115
|
C | T | 1 | a0010c0014t0001g0076 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2584-379C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163115 | ||||||
| chr12:163152
|
T | C | 90 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(87): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.2584-342T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163152 | ||||||
| chr12:163160
|
A | G | 90 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(87): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.2584-334A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163160 | ||||||
| chr12:163166
|
A | G | 95 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(92): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2584-328A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163166 | ||||||
| chr12:163166
|
AACCCCTC others(54): Show |
A | 2 | a0002c0001t0001g0010a0005c0018t0001g0248 | 2 | HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2584-315_2584-255d others(63): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163166 | |||||
| chr12:163179
|
T | C | 5 | a0001c0003t0002g0219a0001c0003t0010g0155a0001c0003t0010g0232others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2584-315T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163179 | ||||||
| chr12:163182
|
T | TCCCTCCA others(2710): Show |
1 | a0001c0002t0002g0039 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2584-292_2584-291i others(2719): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163182 | |||||
| chr12:163200
|
G | C | 2 | a0003c0005t0019g0226a0007c0021t0004g0253 | 2 | HG00733.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2584-294G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163200 | ||||||
| chr12:163200
|
G | GCCCTCCC others(22): Show |
1 | a0002c0001t0003g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2584-284_2584-283i others(31): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163200 | |||||
| chr12:163207
|
C | CCCTCTCC others(3338): Show |
1 | a0001c0006t0010g0209 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2584-286_2584-285i others(3347): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163207 | |||||
| chr12:163209
|
T | TCTCCCTC others(3266): Show |
1 | a0001c0006t0002g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2584-284_2584-283i others(3275): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163209 | |||||
| chr12:163209
|
T | TCTCCTCC others(3222): Show |
1 | a0001c0002t0002g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2584-284_2584-283i others(3231): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163209 | |||||
| chr12:163211
|
C | CCCCTCCA others(345): Show |
8 | a0001c0003t0001g0225a0001c0003t0005g0193a0002c0001t0005g0007others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2584-159_2584-158i others(354): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163211 | |||||
| chr12:163211
|
C | CCCCTCCA others(377): Show |
4 | a0001c0033t0013g0147a0002c0001t0005g0005a0002c0015t0046g0224others(1): Show | 4 | HG01167.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2584-159_2584-158i others(386): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163211 | |||||
| chr12:163211
|
C | CCCCTCCA others(441): Show |
1 | a0003c0010t0019g0178 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2584-159_2584-158i others(450): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163211 | |||||
| chr12:163211
|
C | CCCCTCCA others(313): Show |
2 | a0002c0001t0005g0014a0002c0001t0013g0011 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2584-159_2584-158i others(322): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163211 | |||||
| chr12:163211
|
C | CCCT | 5 | a0001c0003t0002g0219a0001c0004t0016g0223a0002c0001t0016g0121others(2): Show | 5 | HG00733.hp1 HG01258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2584-281_2584-280i others(5): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163211 | |||||
| chr12:163211
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.2584-283C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163211 | ||||||
| chr12:163229
|
C | CCCCTCCC others(922): Show |
1 | a0001c0004t0011g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2584-238_2584-237i others(931): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163229 | |||||
| chr12:163229
|
C | CCCCTCCC others(826): Show |
2 | a0001c0003t0011g0138a0001c0037t0011g0194 | 2 | HG03017.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2584-238_2584-237i others(835): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163229 | |||||
| chr12:163229
|
C | CCCCTCCC others(922): Show |
1 | a0002c0001t0011g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2584-238_2584-237i others(931): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163229 | |||||
| chr12:163229
|
C | CCCCTCCC others(3146): Show |
1 | a0002c0001t0003g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2584-255_2584-254i others(3155): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163229 | |||||
| chr12:163229
|
C | G | 4 | a0001c0003t0002g0219a0001c0004t0016g0223a0001c0004t0058g0185others(1): Show | 4 | HG01258.hp1 HG02630.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2584-265C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163229 | ||||||
| chr12:163240
|
C | CCCCTCCA others(81): Show |
1 | a0001c0059t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(90): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3363): Show |
1 | a0001c0003t0001g0113 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3372): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3116): Show |
2 | a0001c0003t0007g0003a0001c0003t0007g0004 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3125): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3148): Show |
1 | a0003c0010t0007g0268 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3157): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(612): Show |
1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(621): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3176): Show |
2 | a0001c0002t0002g0008a0003c0017t0002g0069 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3185): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3114): Show |
1 | a0008c0016t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3123): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3115): Show |
1 | a0016c0057t0014g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3124): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3304): Show |
1 | a0022c0038t0007g0255 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3313): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3176): Show |
2 | a0001c0002t0002g0035a0001c0002t0002g0066 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3185): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3083): Show |
1 | a0023c0039t0030g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3092): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(2892): Show |
1 | a0003c0017t0002g0089 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(2901): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3329): Show |
1 | a0001c0006t0002g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3338): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3342): Show |
1 | a0001c0002t0002g0239 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3351): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3330): Show |
6 | a0001c0002t0002g0098a0001c0002t0002g0127a0001c0002t0002g0205others(3): Show | 6 | HG00408.hp1 HG00741.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3339): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3333): Show |
1 | a0018c0054t0014g0279 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3342): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3301): Show |
1 | a0001c0006t0002g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3310): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3363): Show |
3 | a0001c0003t0001g0045a0001c0003t0001g0157a0001c0003t0001g0206 | 3 | HG01975.hp2 HG01993.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3372): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3329): Show |
1 | a0001c0006t0002g0196 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3338): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3050): Show |
1 | a0001c0006t0002g0189 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3059): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(4051): Show |
1 | a0003c0017t0015g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(4060): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3175): Show |
1 | a0007c0049t0002g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3184): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3426): Show |
1 | a0001c0006t0002g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3435): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3298): Show |
1 | a0001c0006t0049g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3307): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3330): Show |
9 | a0001c0002t0002g0096a0001c0002t0002g0114a0001c0002t0002g0123others(6): Show | 9 | HG01517.hp2 HG01952.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3339): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3361): Show |
1 | a0001c0002t0044g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3370): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3361): Show |
1 | a0001c0002t0043g0131 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3370): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3301): Show |
1 | a0001c0002t0002g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3310): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3330): Show |
1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3339): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3336): Show |
2 | a0002c0009t0002g0080a0002c0009t0002g0081 | 2 | HG02273.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3345): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3363): Show |
1 | a0001c0002t0002g0125 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3372): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3362): Show |
1 | a0001c0002t0002g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3371): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3362): Show |
1 | a0001c0002t0003g0174 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3371): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3298): Show |
1 | a0001c0006t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2584-252_2584-251i others(3307): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(612): Show |
1 | a0002c0040t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(621): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(1284): Show |
1 | a0001c0002t0048g0105 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2584-252_2584-251i others(1293): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(3301): Show |
4 | a0001c0002t0002g0099a0001c0002t0002g0100a0001c0002t0002g0112others(1): Show | 4 | NA18962.hp1 NA18963.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3310): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCCCTCCA others(4063): Show |
1 | a0001c0002t0002g0001 | 2 | HG02027.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2584-252_2584-251i others(4072): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | CCTCCACA others(369): Show |
1 | a0001c0019t0034g0244 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2584-253_2584-252i others(378): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163240 | |||||
| chr12:163240
|
C | T | 3 | a0001c0002t0002g0039a0001c0002t0002g0179a0001c0006t0010g0209 | 3 | HG01516.hp1 NA18959.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2584-254C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163240 | ||||||
| chr12:163241
|
C | CCCTCCAC others(19): Show |
22 | a0001c0002t0002g0133a0001c0002t0002g0137a0001c0002t0002g0167others(19): Show | 22 | HG00099.hp1 HG00735.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.2584-252_2584-251i others(28): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163241 | |||||
| chr12:163241
|
C | CCCTCCAC others(3367): Show |
2 | a0008c0016t0007g0058a0008c0016t0061g0015 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2584-252_2584-251i others(3376): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163241 | |||||
| chr12:163250
|
A | ACAGAACC others(1610): Show |
1 | a0002c0001t0020g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2584-234_2584-233i others(1619): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163250 | |||||
| chr12:163261
|
C | CCCCCTCC others(249): Show |
1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2584-230_2584-229i others(258): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163261 | |||||
| chr12:163261
|
C | CCCCTCCC others(3117): Show |
1 | a0001c0004t0003g0082 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2584-223_2584-222i others(3126): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163261 | |||||
| chr12:163261
|
C | G | 10 | a0001c0003t0002g0219a0001c0003t0011g0138a0001c0004t0011g0200others(7): Show | 10 | HG00733.hp1 HG01258.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2584-233C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163261 | ||||||
| chr12:163270
|
TCCC | T | 51 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(48): Show | 52 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.2584-222_2584-220d others(5): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163270 | |||||
| chr12:163272
|
C | CCCCTCCA others(3179): Show |
1 | a0004c0008t0003g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3188): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCCTCCA others(3089): Show |
1 | a0008c0035t0007g0135 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3098): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCCTCCA others(3273): Show |
1 | a0001c0002t0047g0201 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3282): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(733): Show |
1 | a0002c0001t0002g0143 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(742): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(792): Show |
1 | a0001c0003t0001g0176 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(801): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(790): Show |
2 | a0001c0003t0001g0044a0001c0003t0001g0088 | 2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.2584-202_2584-201i others(799): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(982): Show |
1 | a0010c0014t0003g0002 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(991): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(982): Show |
1 | a0002c0001t0006g0175 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(991): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1174): Show |
1 | a0002c0001t0003g0041 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1183): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1046): Show |
1 | a0002c0001t0002g0260 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1055): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(982): Show |
6 | a0002c0001t0002g0120a0002c0001t0003g0181a0002c0001t0003g0234others(3): Show | 6 | HG01993.hp2 HG03669.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2584-202_2584-201i others(991): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1517): Show |
1 | a0002c0001t0003g0216 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1526): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1270): Show |
1 | a0002c0001t0003g0183 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1279): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1142): Show |
1 | a0002c0001t0003g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1151): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(377): Show |
1 | a0013c0022t0001g0259 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(386): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(790): Show |
2 | a0001c0003t0001g0141a0001c0003t0001g0172 | 2 | HG01496.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.2584-202_2584-201i others(799): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(790): Show |
6 | a0001c0003t0001g0086a0001c0003t0001g0111a0001c0003t0001g0126others(3): Show | 6 | HG01346.hp1 HG01934.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2584-202_2584-201i others(799): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1110): Show |
1 | a0002c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1119): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1110): Show |
1 | a0001c0044t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1119): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1081): Show |
1 | a0001c0003t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1090): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1109): Show |
1 | a0003c0010t0002g0203 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1118): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1014): Show |
2 | a0001c0003t0012g0049a0003c0010t0012g0034 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2584-202_2584-201i others(1023): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1110): Show |
2 | a0006c0012t0001g0265a0006c0012t0032g0264 | 2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2584-202_2584-201i others(1119): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1046): Show |
1 | a0001c0004t0035g0030 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1055): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1141): Show |
2 | a0001c0042t0001g0243a0002c0001t0001g0184 | 2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.2584-202_2584-201i others(1150): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1205): Show |
1 | a0013c0022t0001g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1214): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(729): Show |
1 | a0002c0001t0002g0171 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(738): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(537): Show |
1 | a0001c0004t0002g0142 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(546): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1080): Show |
1 | a0001c0003t0002g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1089): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1076): Show |
1 | a0001c0004t0012g0022 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1085): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1077): Show |
1 | a0001c0004t0012g0021 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1086): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(470): Show |
1 | a0025c0027t0038g0040 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(479): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1427): Show |
1 | a0001c0025t0040g0148 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1436): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1552): Show |
1 | a0011c0058t0027g0272 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1561): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1488): Show |
1 | a0020c0047t0042g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1497): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(1454): Show |
1 | a0001c0003t0004g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1463): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(534): Show |
2 | a0003c0005t0025g0024a0005c0013t0025g0115 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2584-202_2584-201i others(543): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(886): Show |
1 | a0002c0015t0031g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(895): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(275): Show |
1 | a0001c0004t0016g0223 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(284): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | CCCTCCCT others(630): Show |
3 | a0003c0005t0013g0036a0003c0005t0023g0068a0003c0005t0023g0245 | 3 | HG02615.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2584-202_2584-201i others(639): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163272 | |||||
| chr12:163272
|
C | T | 9 | a0001c0003t0007g0003a0001c0003t0007g0004a0001c0006t0002g0188others(6): Show | 9 | HG00733.hp2 HG01168.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2584-222C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163272 | ||||||
| chr12:163273
|
C | CCCTCCAC others(3115): Show |
1 | a0004c0008t0001g0173 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3124): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3301): Show |
1 | a0004c0008t0001g0129 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3310): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3147): Show |
1 | a0004c0008t0002g0130 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3156): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3176): Show |
1 | a0004c0008t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3185): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3147): Show |
3 | a0001c0002t0002g0182a0001c0002t0002g0240a0004c0008t0052g0247 | 3 | HG00099.hp1 HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2584-220_2584-219i others(3156): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3147): Show |
1 | a0021c0032t0001g0108 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3156): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3302): Show |
1 | a0002c0009t0002g0262 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3311): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3237): Show |
1 | a0002c0001t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3246): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3301): Show |
1 | a0002c0009t0002g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3310): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3272): Show |
3 | a0001c0002t0002g0133a0001c0002t0002g0137a0001c0002t0002g0167 | 3 | HG02698.hp2 HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2584-220_2584-219i others(3281): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3336): Show |
1 | a0002c0009t0002g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3345): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3333): Show |
1 | a0001c0006t0002g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3342): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3301): Show |
1 | a0001c0034t0001g0214 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3310): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCCTCCAC others(3392): Show |
1 | a0001c0006t0002g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2584-220_2584-219i others(3401): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163273
|
C | CCTCCCTC others(494): Show |
1 | a0001c0002t0002g0039 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(503): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163273 | |||||
| chr12:163275
|
T | TCCACAGA others(495): Show |
1 | a0007c0021t0001g0230 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2584-217_2584-216i others(504): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163275 | |||||
| chr12:163282
|
A | ACAGAACC others(950): Show |
1 | a0026c0026t0003g0165 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(959): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163282 | |||||
| chr12:163282
|
A | ACAGAACC others(1673): Show |
1 | a0002c0001t0006g0085 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1682): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163282 | |||||
| chr12:163282
|
A | ACAGAACC others(1704): Show |
4 | a0002c0001t0006g0097a0004c0011t0006g0093a0004c0011t0006g0128others(1): Show | 4 | NA18943.hp2 NA18973.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2584-202_2584-201i others(1713): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163282 | |||||
| chr12:163282
|
A | ACAGAACC others(918): Show |
1 | a0002c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(927): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163282 | |||||
| chr12:163282
|
A | ACAGAACC others(1142): Show |
1 | a0002c0001t0016g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(1151): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163282 | |||||
| chr12:163282
|
A | ACAGAACC others(278): Show |
1 | a0002c0001t0003g0140 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(287): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163282 | |||||
| chr12:163282
|
A | ACAGAACC others(723): Show |
1 | a0001c0004t0058g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2584-202_2584-201i others(732): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163282 | |||||
| chr12:163282
|
A | ACAGAACC others(723): Show |
1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2584-202_2584-201i others(732): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163282 | |||||
| chr12:163282
|
A | T | 2 | a0001c0019t0034g0244a0007c0021t0001g0230 | 2 | HG01168.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2584-212A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163282 | ||||||
| chr12:163293
|
C | G | 40 | a0001c0002t0002g0254a0001c0003t0001g0101a0001c0003t0001g0204others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.2584-201C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163293 | ||||||
| chr12:163298
|
C | CCCCTCTC others(2548): Show |
1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2584-191_2584-190i others(2557): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163298 | |||||
| chr12:163304
|
C | CCCCTCCA others(464): Show |
1 | a0001c0041t0056g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2584-188_2584-187i others(473): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(1203): Show |
1 | a0001c0003t0001g0101 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2584-159_2584-158i others(1212): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(756): Show |
1 | a0001c0007t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2584-159_2584-158i others(765): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(633): Show |
1 | a0002c0001t0050g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2584-159_2584-158i others(642): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(886): Show |
2 | a0003c0010t0015g0263a0003c0010t0015g0266 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2584-159_2584-158i others(895): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(694): Show |
1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2584-159_2584-158i others(703): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(662): Show |
2 | a0003c0046t0001g0229a0005c0031t0001g0057 | 2 | HG01346.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2584-159_2584-158i others(671): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(590): Show |
1 | a0003c0005t0019g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2584-159_2584-158i others(599): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(1771): Show |
1 | a0007c0021t0004g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2584-170_2584-169i others(1780): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(793): Show |
1 | a0001c0024t0001g0032 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2584-170_2584-169i others(802): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(665): Show |
3 | a0002c0001t0001g0202a0009c0020t0001g0211a0012c0023t0018g0276 | 3 | HG01070.hp1 HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2584-170_2584-169i others(674): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(537): Show |
1 | a0009c0051t0001g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2584-170_2584-169i others(546): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(1334): Show |
1 | a0003c0045t0045g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2584-170_2584-169i others(1343): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(406): Show |
1 | a0001c0004t0002g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2584-170_2584-169i others(415): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | CCCTCCCT others(539): Show |
1 | a0004c0011t0004g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2584-170_2584-169i others(548): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163304 | |||||
| chr12:163304
|
C | T | 148 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2584-190C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163304 | ||||||
| chr12:163314
|
A | ACAGAACC others(595): Show |
1 | a0019c0052t0014g0278 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2584-159_2584-158i others(604): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163314 | |||||
| chr12:163314
|
A | ACAGAACC others(470): Show |
1 | a0003c0005t0012g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2584-159_2584-158i others(479): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163314 | |||||
| chr12:163314
|
A | T | 1 | a0001c0004t0016g0223 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2584-180A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163314 | ||||||
| chr12:163325
|
C | G | 45 | a0001c0003t0001g0267a0001c0003t0002g0219a0001c0003t0010g0155others(42): Show | 45 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.2584-169C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163325 | ||||||
| chr12:163336
|
T | C | 80 | a0001c0003t0001g0204a0001c0003t0001g0267a0001c0003t0002g0060others(77): Show | 80 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.2584-158T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163336 | ||||||
| chr12:163353
|
C | T | 3 | a0001c0002t0002g0240a0008c0016t0007g0058a0008c0016t0061g0015 | 3 | HG01175.hp1 HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2584-141C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163353 | ||||||
| chr12:163357
|
C | G | 46 | a0001c0003t0001g0267a0001c0003t0002g0219a0001c0003t0010g0155others(43): Show | 46 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2584-137C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163357 | ||||||
| chr12:163368
|
T | C | 80 | a0001c0003t0001g0204a0001c0003t0001g0267a0001c0003t0002g0060others(77): Show | 80 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.2584-126T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163368 | ||||||
| chr12:163370
|
C | CTCCCTCC others(943): Show |
1 | a0001c0004t0003g0082 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(952): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163370 | |||||
| chr12:163370
|
C | CTCCCTCC others(911): Show |
1 | a0002c0001t0003g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(920): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163370 | |||||
| chr12:163371
|
T | TCCCTCCA others(2462): Show |
1 | a0002c0040t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(2471): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163371 | |||||
| chr12:163376
|
C | CCACAGAA others(144): Show |
2 | a0001c0003t0002g0219a0002c0001t0016g0121 | 2 | HG04228.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(153): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1011): Show |
1 | a0010c0014t0001g0076 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1020): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1526): Show |
1 | a0001c0003t0001g0204 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1535): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1011): Show |
1 | a0002c0001t0036g0161 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1020): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1733): Show |
1 | a0017c0053t0026g0275 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1742): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1011): Show |
2 | a0002c0009t0002g0213a0010c0014t0003g0043 | 2 | HG00438.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(1020): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1011): Show |
1 | a0002c0001t0002g0119 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1020): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1733): Show |
2 | a0002c0001t0006g0151a0004c0011t0006g0132 | 2 | HG00438.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(1742): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1234): Show |
1 | a0002c0001t0021g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1243): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(979): Show |
1 | a0004c0011t0003g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(988): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(723): Show |
1 | a0001c0003t0039g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(732): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1110): Show |
2 | a0001c0003t0002g0060a0001c0003t0002g0102 | 2 | HG02155.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(1119): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(563): Show |
1 | a0006c0012t0004g0065 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(572): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(645): Show |
1 | a0012c0023t0017g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(654): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(54): Show |
1 | a0001c0004t0016g0223 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(63): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(22): Show |
1 | a0011c0058t0027g0272 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(31): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(532): Show |
1 | a0001c0007t0001g0122 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(541): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(371): Show |
1 | a0003c0005t0062g0073 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(380): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(723): Show |
1 | a0002c0001t0004g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(732): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1136): Show |
1 | a0002c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1145): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(304): Show |
2 | a0001c0003t0010g0155a0001c0003t0010g0232 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(313): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1616): Show |
1 | a0001c0007t0001g0103 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1625): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(947): Show |
1 | a0002c0001t0041g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(956): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1093): Show |
1 | a0001c0004t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1102): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(657): Show |
1 | a0001c0004t0003g0197 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(666): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(752): Show |
1 | a0001c0007t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(761): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(720): Show |
1 | a0001c0007t0001g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(729): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(688): Show |
1 | a0001c0004t0037g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(697): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(624): Show |
1 | a0002c0001t0022g0038 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(633): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(531): Show |
2 | a0001c0007t0001g0042a0001c0007t0001g0149 | 2 | NA18957.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(540): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(688): Show |
1 | a0001c0004t0003g0198 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(697): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(656): Show |
6 | a0001c0004t0001g0235a0001c0007t0001g0107a0001c0007t0001g0117others(3): Show | 6 | HG03831.hp1 HG04115.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2584-107_2584-106i others(665): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(752): Show |
1 | a0001c0007t0001g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(761): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(720): Show |
1 | a0011c0055t0018g0271 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(729): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(655): Show |
1 | a0001c0007t0001g0153 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(664): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(691): Show |
1 | a0003c0005t0059g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(700): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(659): Show |
1 | a0003c0005t0003g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(668): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(973): Show |
1 | a0001c0004t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(982): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(435): Show |
4 | a0001c0004t0004g0031a0007c0048t0001g0221a0014c0029t0054g0059others(1): Show | 4 | HG01081.hp2 HG01496.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2584-107_2584-106i others(444): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(403): Show |
5 | a0003c0005t0002g0252a0003c0005t0009g0009a0003c0005t0009g0055others(2): Show | 5 | HG01167.hp2 HG02572.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2584-107_2584-106i others(412): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(499): Show |
2 | a0003c0005t0009g0077a0003c0005t0009g0281 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(508): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(435): Show |
2 | a0002c0001t0004g0028a0002c0001t0004g0029 | 2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(444): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(560): Show |
1 | a0001c0019t0001g0139 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(569): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(403): Show |
2 | a0002c0001t0009g0064a0002c0001t0009g0192 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(412): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(563): Show |
1 | a0002c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(572): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(531): Show |
6 | a0002c0001t0008g0020a0002c0001t0008g0025a0002c0001t0008g0052others(3): Show | 6 | HG01074.hp1 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2584-107_2584-106i others(540): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(499): Show |
1 | a0002c0001t0008g0026 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(508): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(528): Show |
1 | a0001c0007t0001g0152 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(537): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(339): Show |
3 | a0001c0003t0001g0267a0003c0005t0028g0228a0005c0013t0009g0246 | 3 | HG03540.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(348): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(1334): Show |
1 | a0001c0004t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(1343): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(339): Show |
3 | a0001c0004t0060g0217a0002c0001t0024g0017a0002c0001t0024g0177 | 3 | HG02630.hp2 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2584-107_2584-106i others(348): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(435): Show |
1 | a0002c0001t0008g0023 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2584-107_2584-106i others(444): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(243): Show |
1 | a0001c0043t0004g0063 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2584-107_2584-106i others(252): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(22): Show |
78 | a0001c0003t0001g0044a0001c0003t0001g0086a0001c0003t0001g0088others(75): Show | 78 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2584-110_2584-109i others(31): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163376
|
C | CCACAGAA others(21): Show |
1 | a0001c0003t0002g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2584-110_2584-109i others(30): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 163376 | |||||
| chr12:163388
|
G | A | 87 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2584-106G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163388 | ||||||
| chr12:163434
|
G | A | 8 | a0001c0003t0004g0166a0001c0004t0003g0082a0001c0025t0040g0148others(5): Show | 8 | HG00673.hp2 HG00733.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.2584-60G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | chr12 | 163434 | ||||||
| chr12:163677
|
C | A | 1 | a0002c0001t0003g0234 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2709+58C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 163677 | ||||||
| chr12:163824
|
A | G | 216 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.2709+205A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 163824 | ||||||
| chr12:163871
|
A | G | 1 | a0009c0020t0001g0238 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2709+252A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 163871 | ||||||
| chr12:163988
|
C | T | 93 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(90): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2709+369C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 163988 | ||||||
| chr12:164049
|
T | C | 2 | a0001c0002t0002g0035a0001c0002t0002g0066 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2709+430T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164049 | ||||||
| chr12:164087
|
T | C | 3 | a0001c0003t0001g0267a0003c0005t0019g0226a0003c0005t0028g0228 | 3 | HG02922.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2709+468T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164087 | ||||||
| chr12:164402
|
TCC | T | 6 | a0001c0004t0003g0082a0002c0001t0003g0215a0002c0001t0022g0038others(3): Show | 6 | HG01517.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2709+786_2709+787d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 164402 | |||||
| chr12:164417
|
C | A | 1 | a0002c0001t0003g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2709+798C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164417 | ||||||
| chr12:164468
|
C | A | 2 | a0001c0004t0058g0185a0003c0010t0020g0078 | 2 | HG01884.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2709+849C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164468 | ||||||
| chr12:164487
|
C | T | 1 | a0002c0001t0036g0161 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2709+868C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164487 | ||||||
| chr12:164707
|
G | A | 1 | a0001c0007t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2710-727G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164707 | ||||||
| chr12:164843
|
T | C | 1 | a0001c0002t0002g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2710-591T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164843 | ||||||
| chr12:164855
|
C | T | 5 | a0001c0003t0002g0219a0001c0003t0010g0155a0001c0003t0010g0232others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2710-579C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164855 | ||||||
| chr12:164859
|
CAAGAT | C | 5 | a0001c0003t0002g0219a0001c0003t0010g0155a0001c0003t0010g0232others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2710-572_2710-568d others(7): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 164859 | |||||
| chr12:164964
|
T | G | 1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2710-470T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 164964 | ||||||
| chr12:164970
|
AGAG | A | 5 | a0001c0004t0035g0030a0001c0044t0001g0050a0002c0001t0001g0019others(2): Show | 5 | HG01516.hp2 HG01891.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2710-459_2710-457d others(5): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 164970 | |||||
| chr12:165406
|
G | C | 264 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2710-28G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 9/13 | chr12 | 165406 | ||||||
| chr12:165530
|
G | GAGTGTAA others(13): Show |
7 | a0008c0016t0007g0037a0008c0016t0007g0058a0008c0016t0061g0015others(4): Show | 7 | HG00280.hp2 HG00733.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.2809+13_2809+32dup others(20): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 165530 | |||||
| chr12:165530
|
GAGTGTAA others(13): Show |
G | 1 | a0020c0047t0042g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2809+13_2809+32del others(20): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 165530 | |||||
| chr12:165615
|
G | A | 1 | a0004c0011t0004g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2809+82G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 10/13 | chr12 | 165615 | ||||||
| chr12:165673
|
T | C | 76 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(73): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2810-56T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 10/13 | chr12 | 165673 | ||||||
| chr12:165899
|
A | G | 76 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(73): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2971+9A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 165899 | ||||||
| chr12:165995
|
C | T | 3 | a0001c0004t0003g0082a0002c0001t0003g0215a0002c0040t0029g0156 | 3 | HG01517.hp1 HG02145.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2971+105C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 165995 | ||||||
| chr12:166074
|
C | A | 7 | a0001c0003t0007g0003a0001c0003t0007g0004a0002c0001t0004g0027others(4): Show | 7 | HG00597.hp2 HG01243.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2971+184C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166074 | ||||||
| chr12:166104
|
C | G | 76 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(73): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2971+214C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166104 | ||||||
| chr12:166107
|
G | A | 1 | a0005c0018t0001g0248 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2971+217G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166107 | ||||||
| chr12:166142
|
C | T | 1 | a0004c0008t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2971+252C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166142 | ||||||
| chr12:166227
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2971+337G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166227 | ||||||
| chr12:166465
|
T | C | 1 | a0004c0011t0004g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2971+575T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166465 | ||||||
| chr12:166496
|
C | T | 1 | a0008c0016t0007g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2971+606C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166496 | ||||||
| chr12:166853
|
C | T | 96 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(93): Show | 97 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.2971+963C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166853 | ||||||
| chr12:166859
|
C | T | 3 | a0001c0002t0002g0008a0001c0004t0060g0217a0003c0017t0002g0069 | 3 | HG02647.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2971+969C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166859 | ||||||
| chr12:166874
|
G | A | 2 | a0001c0002t0002g0008a0003c0017t0002g0069 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2971+984G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166874 | ||||||
| chr12:166970
|
A | C | 1 | a0003c0017t0002g0089 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2971+1080A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166970 | ||||||
| chr12:166977
|
A | C | 3 | a0001c0004t0058g0185a0002c0015t0031g0207a0003c0010t0020g0078 | 3 | HG01884.hp2 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2971+1087A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 166977 | ||||||
| chr12:167054
|
G | A | 88 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(85): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2971+1164G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167054 | ||||||
| chr12:167170
|
G | C | 115 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0086others(112): Show | 115 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.2971+1280G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167170 | ||||||
| chr12:167171
|
G | A | 2 | a0003c0010t0002g0203a0013c0022t0001g0237 | 2 | HG00099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.2971+1281G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167171 | ||||||
| chr12:167234
|
C | T | 3 | a0002c0001t0020g0071a0002c0015t0046g0224a0014c0028t0001g0062 | 3 | HG01167.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2971+1344C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167234 | ||||||
| chr12:167283
|
C | T | 1 | a0002c0009t0002g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2971+1393C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167283 | ||||||
| chr12:167302
|
G | A | 1 | a0024c0036t0057g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2971+1412G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167302 | ||||||
| chr12:167541
|
G | A | 3 | a0002c0001t0020g0071a0002c0015t0046g0224a0014c0028t0001g0062 | 3 | HG01167.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2972-1472G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167541 | ||||||
| chr12:167558
|
G | A | 3 | a0002c0001t0020g0071a0002c0015t0046g0224a0014c0028t0001g0062 | 3 | HG01167.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2972-1455G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167558 | ||||||
| chr12:167576
|
G | GAAA | 84 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(81): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2972-1425_2972-142 others(7): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | 167576 | |||||
| chr12:167814
|
A | G | 4 | a0004c0011t0006g0093a0004c0011t0006g0128a0004c0011t0006g0132others(1): Show | 4 | NA18943.hp2 NA18973.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2972-1199A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167814 | ||||||
| chr12:167840
|
C | T | 1 | a0001c0003t0001g0141 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2972-1173C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167840 | ||||||
| chr12:167896
|
A | C | 2 | a0002c0001t0021g0163a0002c0001t0021g0164 | 2 | HG00621.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2972-1117A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 167896 | ||||||
| chr12:168016
|
C | T | 92 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(89): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.2972-997C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168016 | ||||||
| chr12:168161
|
G | A | 4 | a0001c0007t0001g0083a0001c0007t0001g0107a0001c0007t0001g0118others(1): Show | 4 | HG00597.hp1 HG02015.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.2972-852G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168161 | ||||||
| chr12:168206
|
T | G | 2 | a0003c0005t0019g0226a0003c0010t0019g0178 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2972-807T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168206 | ||||||
| chr12:168258
|
G | A | 1 | a0001c0003t0001g0045 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2972-755G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168258 | ||||||
| chr12:168298
|
A | C | 98 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(95): Show | 99 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.2972-715A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168298 | ||||||
| chr12:168367
|
G | A | 3 | a0002c0001t0020g0071a0002c0015t0046g0224a0014c0028t0001g0062 | 3 | HG01167.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2972-646G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168367 | ||||||
| chr12:168378
|
T | C | 270 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.2972-635T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168378 | ||||||
| chr12:168413
|
G | A | 1 | a0001c0003t0039g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2972-600G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168413 | ||||||
| chr12:168502
|
T | A | 18 | a0001c0003t0012g0049a0001c0004t0012g0021a0001c0004t0012g0022others(15): Show | 18 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.2972-511T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168502 | ||||||
| chr12:168542
|
T | A | 25 | a0001c0003t0012g0049a0001c0004t0012g0021a0001c0004t0012g0022others(22): Show | 25 | HG01106.hp1 HG01243.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.2972-471T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168542 | ||||||
| chr12:168566
|
TAAG | T | 3 | a0001c0041t0056g0072a0003c0005t0019g0226a0003c0010t0019g0178 | 3 | HG02922.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2972-446_2972-444d others(5): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168566 | ||||||
| chr12:168637
|
G | A | 7 | a0002c0001t0004g0027a0002c0001t0004g0028a0002c0001t0004g0029others(4): Show | 7 | HG01106.hp1 HG01243.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.2972-376G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168637 | ||||||
| chr12:168702
|
C | T | 1 | a0001c0041t0056g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2972-311C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168702 | ||||||
| chr12:168756
|
A | C | 3 | a0001c0004t0058g0185a0002c0015t0031g0207a0003c0010t0020g0078 | 3 | HG01884.hp2 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2972-257A>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168756 | ||||||
| chr12:168760
|
C | T | 1 | a0002c0040t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2972-253C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168760 | ||||||
| chr12:168820
|
C | G | 89 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(86): Show | 90 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2972-193C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168820 | ||||||
| chr12:168826
|
TGC | T | 3 | a0001c0004t0058g0185a0002c0015t0031g0207a0003c0010t0020g0078 | 3 | HG01884.hp2 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2972-185_2972-184d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | 168826 | |||||
| chr12:168841
|
G | A | 1 | a0001c0002t0002g0123 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2972-172G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168841 | ||||||
| chr12:168916
|
C | T | 24 | a0001c0004t0001g0235a0001c0004t0001g0277a0001c0004t0003g0197others(21): Show | 24 | HG00597.hp1 HG01070.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.2972-97C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168916 | ||||||
| chr12:168961
|
T | C | 6 | a0001c0003t0004g0166a0001c0025t0040g0148a0002c0001t0022g0038others(3): Show | 6 | HG00673.hp2 HG00733.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2972-52T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 11/13 | chr12 | 168961 | ||||||
| chr12:169135
|
T | C | 3 | a0002c0001t0020g0071a0002c0015t0046g0224a0014c0028t0001g0062 | 3 | HG01167.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3064+30T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169135 | ||||||
| chr12:169210
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3064+105C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169210 | ||||||
| chr12:169276
|
G | A | 6 | a0001c0003t0004g0166a0001c0025t0040g0148a0002c0001t0022g0038others(3): Show | 6 | HG00673.hp2 HG00733.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3064+171G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169276 | ||||||
| chr12:169328
|
A | G | 4 | a0001c0002t0002g0098a0001c0002t0002g0127a0001c0002t0002g0205others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3064+223A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169328 | ||||||
| chr12:169439
|
G | T | 256 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.3064+334G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169439 | ||||||
| chr12:169640
|
G | A | 1 | a0003c0005t0028g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3064+535G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169640 | ||||||
| chr12:169669
|
C | T | 4 | a0001c0002t0002g0123a0001c0006t0002g0092a0001c0006t0002g0189others(1): Show | 4 | HG02071.hp1 HG02083.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.3064+564C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169669 | ||||||
| chr12:169682
|
C | T | 86 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3064+577C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169682 | ||||||
| chr12:169900
|
C | T | 3 | a0001c0004t0058g0185a0002c0015t0031g0207a0003c0010t0020g0078 | 3 | HG01884.hp2 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3064+795C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169900 | ||||||
| chr12:169968
|
G | A | 2 | a0003c0010t0015g0263a0003c0010t0015g0266 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3064+863G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169968 | ||||||
| chr12:169976
|
C | G | 120 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0086others(117): Show | 120 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.3064+871C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 169976 | ||||||
| chr12:170004
|
G | C | 3 | a0001c0004t0058g0185a0002c0015t0031g0207a0003c0010t0020g0078 | 3 | HG01884.hp2 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3064+899G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170004 | ||||||
| chr12:170112
|
G | C | 1 | a0005c0018t0001g0248 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3065-1000G>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170112 | ||||||
| chr12:170143
|
C | G | 4 | a0008c0035t0007g0135a0016c0057t0014g0274a0022c0038t0007g0255others(1): Show | 4 | HG00280.hp2 HG00733.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.3065-969C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170143 | ||||||
| chr12:170165
|
C | T | 1 | a0001c0002t0002g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3065-947C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170165 | ||||||
| chr12:170292
|
G | A | 240 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.3065-820G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170292 | ||||||
| chr12:170299
|
C | CCT | 4 | a0001c0004t0003g0082a0002c0001t0003g0215a0002c0040t0029g0156others(1): Show | 4 | HG01517.hp1 HG02145.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.3065-812_3065-811d others(4): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 170299 | |||||
| chr12:170314
|
T | G | 2 | a0003c0010t0015g0263a0003c0010t0015g0266 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3065-798T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170314 | ||||||
| chr12:170374
|
G | GT | 203 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.3065-737dupT | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 170374 | |||||
| chr12:170420
|
T | C | 125 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0086others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.3065-692T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170420 | ||||||
| chr12:170509
|
G | A | 1 | a0004c0008t0001g0129 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3065-603G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170509 | ||||||
| chr12:170540
|
G | A | 1 | a0001c0002t0002g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3065-572G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170540 | ||||||
| chr12:170541
|
T | C | 32 | a0001c0003t0001g0267a0001c0003t0012g0049a0001c0004t0004g0031others(29): Show | 32 | HG01243.hp1 HG01496.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.3065-571T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170541 | ||||||
| chr12:170573
|
G | A | 5 | a0001c0003t0010g0155a0001c0003t0010g0232a0001c0004t0016g0223others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.3065-539G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170573 | ||||||
| chr12:170582
|
C | T | 9 | a0002c0001t0001g0191a0002c0001t0008g0020a0002c0001t0008g0023others(6): Show | 9 | HG00735.hp1 HG01074.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.3065-530C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170582 | ||||||
| chr12:170739
|
A | T | 1 | a0001c0004t0012g0022 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3065-373A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170739 | ||||||
| chr12:170780
|
G | A | 2 | a0003c0005t0019g0226a0003c0010t0019g0178 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3065-332G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170780 | ||||||
| chr12:170806
|
C | G | 10 | a0002c0001t0001g0191a0002c0001t0008g0020a0002c0001t0008g0023others(7): Show | 10 | HG00735.hp1 HG01074.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.3065-306C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170806 | ||||||
| chr12:170901
|
G | A | 2 | a0003c0010t0015g0263a0003c0010t0015g0266 | 2 | HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3065-211G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170901 | ||||||
| chr12:170988
|
C | T | 2 | a0002c0001t0008g0020a0002c0001t0008g0026 | 2 | HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.3065-124C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 12/13 | chr12 | 170988 | ||||||
| chr12:171183
|
C | A | 74 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(71): Show | 75 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.3114+22C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171183 | ||||||
| chr12:171345
|
C | T | 1 | a0007c0021t0004g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3114+184C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171345 | ||||||
| chr12:171403
|
C | T | 18 | a0001c0003t0004g0166a0001c0003t0012g0049a0001c0004t0012g0021others(15): Show | 18 | HG00673.hp2 HG00733.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.3114+242C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171403 | ||||||
| chr12:171595
|
C | T | 131 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0086others(128): Show | 131 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.3114+434C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171595 | ||||||
| chr12:171715
|
C | T | 5 | a0001c0004t0060g0217a0002c0001t0024g0017a0002c0001t0024g0177others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3114+554C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171715 | ||||||
| chr12:171739
|
GC | G | 6 | a0001c0003t0007g0003a0001c0003t0007g0004a0001c0042t0001g0243others(3): Show | 6 | HG00597.hp2 HG01106.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.3114+579delC | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171739 | ||||||
| chr12:171883
|
A | G | 13 | a0001c0003t0010g0155a0001c0003t0010g0232a0001c0004t0016g0223others(10): Show | 13 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.3114+722A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171883 | ||||||
| chr12:171943
|
C | T | 1 | a0010c0014t0003g0002 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3114+782C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171943 | ||||||
| chr12:171972
|
A | T | 1 | a0001c0003t0011g0138 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3114+811A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171972 | ||||||
| chr12:171985
|
C | T | 2 | a0001c0002t0043g0131a0001c0002t0044g0084 | 2 | HG02027.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3114+824C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 171985 | ||||||
| chr12:172037
|
T | C | 1 | a0003c0010t0020g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3114+876T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172037 | ||||||
| chr12:172066
|
C | T | 2 | a0002c0001t0020g0071a0003c0010t0020g0078 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3114+905C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172066 | ||||||
| chr12:172067
|
G | A | 4 | a0001c0003t0010g0155a0001c0004t0016g0223a0001c0006t0010g0209others(1): Show | 4 | HG00280.hp1 HG01258.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3114+906G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172067 | ||||||
| chr12:172092
|
C | T | 1 | a0001c0002t0003g0174 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3114+931C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172092 | ||||||
| chr12:172103
|
C | T | 1 | a0005c0013t0009g0246 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3114+942C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172103 | ||||||
| chr12:172119
|
C | T | 1 | a0001c0003t0039g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3114+958C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172119 | ||||||
| chr12:172149
|
A | G | 1 | a0002c0001t0051g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3114+988A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172149 | ||||||
| chr12:172245
|
C | T | 2 | a0001c0004t0060g0217a0002c0001t0024g0017 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3114+1084C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172245 | ||||||
| chr12:172388
|
C | A | 4 | a0003c0005t0009g0077a0003c0005t0009g0281a0003c0005t0062g0073others(1): Show | 4 | HG01952.hp1 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3114+1227C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172388 | ||||||
| chr12:172391
|
G | T | 4 | a0003c0005t0009g0077a0003c0005t0009g0281a0003c0005t0062g0073others(1): Show | 4 | HG01952.hp1 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3114+1230G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172391 | ||||||
| chr12:172403
|
C | G | 2 | a0001c0002t0043g0131a0001c0002t0044g0084 | 2 | HG02027.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3114+1242C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172403 | ||||||
| chr12:172433
|
T | C | 96 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(93): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3114+1272T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172433 | ||||||
| chr12:172488
|
T | C | 1 | a0001c0003t0002g0102 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3114+1327T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172488 | ||||||
| chr12:172497
|
A | G | 268 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.3114+1336A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172497 | ||||||
| chr12:172612
|
C | A | 5 | a0001c0003t0011g0138a0001c0004t0011g0200a0001c0037t0011g0194others(2): Show | 5 | HG03017.hp2 HG03831.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.3114+1451C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172612 | ||||||
| chr12:172706
|
T | A | 1 | a0002c0001t0041g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3114+1545T>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172706 | ||||||
| chr12:172782
|
G | A | 6 | a0001c0003t0007g0003a0001c0003t0007g0004a0001c0042t0001g0243others(3): Show | 6 | HG00597.hp2 HG01106.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.3114+1621G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172782 | ||||||
| chr12:172812
|
C | G | 12 | a0001c0041t0056g0072a0002c0001t0008g0020a0002c0001t0008g0023others(9): Show | 12 | HG01074.hp1 HG01358.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3114+1651C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172812 | ||||||
| chr12:172849
|
G | A | 1 | a0004c0008t0053g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3114+1688G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172849 | ||||||
| chr12:172896
|
G | A | 1 | a0002c0040t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3115-1703G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172896 | ||||||
| chr12:172925
|
C | T | 2 | a0001c0043t0004g0063a0002c0001t0050g0051 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3115-1674C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172925 | ||||||
| chr12:172958
|
G | A | 3 | a0002c0001t0020g0071a0002c0015t0031g0207a0003c0010t0020g0078 | 3 | HG01884.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3115-1641G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 172958 | ||||||
| chr12:173067
|
G | A | 1 | a0001c0006t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3115-1532G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173067 | ||||||
| chr12:173127
|
C | T | 2 | a0001c0003t0001g0113a0001c0003t0001g0206 | 2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3115-1472C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173127 | ||||||
| chr12:173133
|
C | T | 3 | a0002c0001t0020g0071a0002c0015t0031g0207a0003c0010t0020g0078 | 3 | HG01884.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3115-1466C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173133 | ||||||
| chr12:173154
|
T | C | 272 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.3115-1445T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173154 | ||||||
| chr12:173267
|
C | T | 3 | a0003c0010t0015g0263a0003c0010t0015g0266a0003c0017t0015g0056 | 3 | HG01106.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3115-1332C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173267 | ||||||
| chr12:173372
|
G | T | 1 | a0003c0005t0012g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3115-1227G>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173372 | ||||||
| chr12:173488
|
G | A | 9 | a0001c0003t0010g0155a0001c0003t0010g0232a0001c0004t0016g0223others(6): Show | 9 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.3115-1111G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173488 | ||||||
| chr12:173546
|
C | G | 2 | a0001c0002t0043g0131a0001c0002t0044g0084 | 2 | HG02027.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3115-1053C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173546 | ||||||
| chr12:173586
|
G | A | 1 | a0006c0012t0004g0065 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3115-1013G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173586 | ||||||
| chr12:173634
|
G | A | 5 | a0001c0003t0011g0138a0001c0004t0011g0200a0001c0037t0011g0194others(2): Show | 5 | HG03017.hp2 HG03831.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.3115-965G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173634 | ||||||
| chr12:173645
|
C | T | 8 | a0001c0003t0010g0155a0001c0003t0010g0232a0001c0004t0016g0223others(5): Show | 8 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.3115-954C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173645 | ||||||
| chr12:173701
|
G | A | 3 | a0001c0002t0002g0114a0002c0009t0002g0222a0002c0009t0002g0262 | 3 | HG00735.hp2 HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.3115-898G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173701 | ||||||
| chr12:173716
|
C | G | 9 | a0001c0003t0010g0155a0001c0003t0010g0232a0001c0004t0016g0223others(6): Show | 9 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.3115-883C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173716 | ||||||
| chr12:173716
|
C | T | 2 | a0003c0005t0019g0226a0003c0010t0019g0178 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3115-883C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 173716 | ||||||
| chr12:174011
|
C | T | 2 | a0001c0003t0001g0044a0001c0003t0001g0088 | 2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.3115-588C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174011 | ||||||
| chr12:174028
|
G | A | 4 | a0001c0003t0012g0049a0001c0004t0012g0021a0001c0004t0012g0022others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3115-571G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174028 | ||||||
| chr12:174079
|
C | A | 1 | a0002c0015t0046g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3115-520C>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174079 | ||||||
| chr12:174234
|
C | T | 1 | a0001c0007t0001g0153 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3115-365C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174234 | ||||||
| chr12:174250
|
T | C | 2 | a0002c0001t0051g0013a0002c0015t0046g0224 | 2 | HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3115-349T>C | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174250 | ||||||
| chr12:174368
|
C | T | 2 | a0001c0037t0011g0194a0002c0001t0011g0162 | 2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3115-231C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174368 | ||||||
| chr12:174370
|
A | G | 1 | a0001c0004t0058g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3115-229A>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174370 | ||||||
| chr12:174409
|
G | A | 11 | a0001c0003t0010g0155a0001c0003t0010g0232a0001c0004t0016g0223others(8): Show | 11 | HG00280.hp1 HG01074.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3115-190G>A | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174409 | ||||||
| chr12:174411
|
C | G | 1 | a0006c0012t0005g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3115-188C>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174411 | ||||||
| chr12:174447
|
A | T | 2 | a0002c0015t0031g0207a0003c0010t0020g0078 | 2 | HG01884.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3115-152A>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174447 | ||||||
| chr12:174476
|
C | T | 92 | a0001c0002t0002g0001a0001c0002t0002g0008a0001c0002t0002g0035others(89): Show | 93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.3115-123C>T | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174476 | ||||||
| chr12:174568
|
T | G | 1 | a0002c0001t0008g0025 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3115-31T>G | IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 13/13 | chr12 | 174568 |