Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3684 |
|---|---|
| ensemblid | ENSG00000169896.18 |
| hgncid | 6149 |
| symbol | ITGAM |
| name | integrin subunit alpha M |
| refseq_nuc | NM_000632.4 |
| refseq_prot | NP_000623.2 |
| ensembl_nuc | ENST00000544665.9 |
| ensembl_prot | ENSP00000441691.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 31259975 |
| end | 31332877 |
| strand | + |
| ver | v1.2 |
| region | chr16:31259975-31332877 |
| region5000 | chr16:31254975-31337877 |
| regionname0 | ITGAM_chr16_31259975_31332877 |
| regionname5000 | ITGAM_chr16_31254975_31337877 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1152 | 176 | 53 | 36 | 64 | 6 | 15 | 36 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0002 | 0/0 | 1152 | 24 | 10 | 4 | 2 | 0 | 8 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0003 | 0/0 | 1152 | 23 | 15 | 4 | 0 | 2 | 2 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0004 | 0/0 | 1152 | 14 | 5 | 7 | 0 | 2 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0005 | 0/0 | 1152 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0006 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0007 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0008 | 0/0 | 1152 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0009 | 0/0 | 1152 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0010 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3459 | 88 | 20 | 18 | 32 | 4 | 12 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0002 | 0/0 | 3459 | 57 | 3 | 17 | 32 | 2 | 3 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0003 | 0/0 | 3459 | 24 | 10 | 4 | 2 | 0 | 8 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0004 | 0/0 | 3459 | 23 | 15 | 4 | 0 | 2 | 2 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0005 | 0/0 | 3459 | 19 | 19 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0006 | 0/0 | 3459 | 14 | 5 | 7 | 0 | 2 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0007 | 0/0 | 3459 | 9 | 8 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0008 | 0/0 | 3459 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0009 | 0/0 | 3459 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0010 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0011 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0012 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0013 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0014 | 0/0 | 3459 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| c0015 | 0/0 | 3459 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1261 | 76 | 6 | 19 | 32 | 4 | 13 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| t0002 | 0/0 | 1269 | 69 | 14 | 16 | 34 | 2 | 3 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| t0003 | 0/0 | 1261 | 38 | 15 | 11 | 2 | 2 | 8 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| t0004 | 0/0 | 1261 | 35 | 34 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| t0005 | 0/0 | 1274 | 22 | 15 | 3 | 0 | 2 | 2 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| t0006 | 0/0 | 1274 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| t0007 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| t0008 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| t0009 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3459 | 88 | 20 | 18 | 32 | 4 | 12 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0002 | 0/0 | 3459 | 57 | 3 | 17 | 32 | 2 | 3 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0005 | 0/0 | 3459 | 19 | 19 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0007 | 0/0 | 3459 | 9 | 8 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0008 | 0/0 | 3459 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0013 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0002c0003 | 0/0 | 3459 | 24 | 10 | 4 | 2 | 0 | 8 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0003c0004 | 0/0 | 3459 | 23 | 15 | 4 | 0 | 2 | 2 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0004c0006 | 0/0 | 3459 | 14 | 5 | 7 | 0 | 2 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0005c0009 | 0/0 | 3459 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0006c0010 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0007c0011 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0008c0015 | 0/0 | 3459 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0009c0014 | 0/0 | 3459 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0010c0012 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4719 | 74 | 6 | 18 | 32 | 4 | 12 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0001t0002 | 0/0 | 4727 | 11 | 11 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0001t0004 | 0/0 | 4719 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0002t0002 | 0/0 | 4727 | 56 | 3 | 16 | 32 | 2 | 3 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0002t0007 | 0/0 | 4727 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0005t0004 | 0/0 | 4719 | 19 | 19 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0007t0004 | 0/0 | 4719 | 8 | 7 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0007t0009 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0008t0004 | 0/0 | 4719 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0001c0013t0008 | 0/0 | 4727 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0002c0003t0003 | 0/0 | 4719 | 24 | 10 | 4 | 2 | 0 | 8 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0003c0004t0005 | 0/0 | 4732 | 22 | 15 | 3 | 0 | 2 | 2 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0003c0004t0006 | 0/0 | 4732 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0004c0006t0003 | 0/0 | 4719 | 14 | 5 | 7 | 0 | 2 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0005c0009t0002 | 0/0 | 4727 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0006c0010t0004 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0007c0011t0004 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0008c0015t0001 | 0/0 | 4719 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0009c0014t0001 | 0/0 | 4719 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| a0010c0012t0004 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | copy fasta | chr16 | 31254975 | 31337877 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0002t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0005t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0007t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0008t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0008t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0001c0013t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0002c0003t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0003c0004t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0004c0006t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0005c0009t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0005c0009t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0006c0010t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0007c0011t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0008c0015t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0009c0014t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| a0010c0012t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0005 | g0079 | EUR | GBR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00323 | hp1 | a0004 | c0006 | t0003 | g0012 | EUR | FIN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0091 | EUR | FIN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00733 | hp2 | a0004 | c0006 | t0003 | g0003 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00738 | hp1 | a0001 | c0002 | t0007 | g0030 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00738 | hp2 | a0004 | c0006 | t0003 | g0014 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00741 | hp1 | a0004 | c0006 | t0003 | g0004 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG00741 | hp2 | a0002 | c0003 | t0003 | g0119 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01070 | hp2 | a0009 | c0014 | t0001 | g0225 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01106 | hp1 | a0002 | c0003 | t0003 | g0124 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0120 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01109 | hp1 | a0004 | c0006 | t0003 | g0002 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01109 | hp2 | a0003 | c0004 | t0006 | g0034 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01175 | hp1 | a0003 | c0004 | t0005 | g0037 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01243 | hp1 | a0002 | c0003 | t0003 | g0092 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01255 | hp2 | a0003 | c0004 | t0005 | g0078 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01256 | hp1 | a0004 | c0006 | t0003 | g0006 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01256 | hp2 | a0003 | c0004 | t0005 | g0019 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01258 | hp1 | a0004 | c0006 | t0003 | g0005 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01433 | hp2 | a0004 | c0006 | t0003 | g0008 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01496 | hp2 | a0001 | c0007 | t0004 | g0023 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01516 | hp1 | a0004 | c0006 | t0003 | g0015 | EUR | IBS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0035 | EUR | IBS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01891 | hp1 | a0002 | c0003 | t0003 | g0127 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01891 | hp2 | a0001 | c0008 | t0004 | g0140 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0048 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02040 | hp2 | a0005 | c0009 | t0002 | g0093 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02055 | hp2 | a0004 | c0006 | t0003 | g0013 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0088 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02129 | hp1 | a0005 | c0009 | t0002 | g0050 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02135 | hp2 | a0002 | c0003 | t0003 | g0074 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02145 | hp1 | a0001 | c0005 | t0004 | g0156 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02145 | hp2 | a0003 | c0004 | t0005 | g0096 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | CDX | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02257 | hp2 | a0003 | c0004 | t0005 | g0086 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02258 | hp2 | a0001 | c0005 | t0004 | g0151 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02280 | hp2 | a0001 | c0005 | t0004 | g0159 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0070 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02451 | hp1 | a0001 | c0013 | t0008 | g0175 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02572 | hp1 | a0002 | c0003 | t0003 | g0016 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02572 | hp2 | a0003 | c0004 | t0005 | g0099 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02615 | hp2 | a0003 | c0004 | t0005 | g0097 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02622 | hp1 | a0002 | c0003 | t0003 | g0123 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02622 | hp2 | a0001 | c0005 | t0004 | g0160 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02630 | hp1 | a0001 | c0005 | t0004 | g0163 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02630 | hp2 | a0002 | c0003 | t0003 | g0113 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02647 | hp1 | a0001 | c0007 | t0004 | g0145 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02647 | hp2 | a0010 | c0012 | t0004 | g0164 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02683 | hp1 | a0002 | c0003 | t0003 | g0080 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02717 | hp1 | a0001 | c0007 | t0004 | g0148 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02723 | hp2 | a0001 | c0005 | t0004 | g0243 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02735 | hp1 | a0003 | c0004 | t0005 | g0031 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0130 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02809 | hp2 | a0001 | c0007 | t0004 | g0146 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02818 | hp1 | a0003 | c0004 | t0005 | g0025 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02886 | hp2 | a0003 | c0004 | t0005 | g0077 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02895 | hp1 | a0004 | c0006 | t0003 | g0009 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02895 | hp2 | a0001 | c0005 | t0004 | g0001 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02896 | hp1 | a0006 | c0010 | t0004 | g0018 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02896 | hp2 | a0003 | c0004 | t0005 | g0105 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02897 | hp1 | a0001 | c0005 | t0004 | g0001 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02897 | hp2 | a0003 | c0004 | t0005 | g0107 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02922 | hp1 | a0001 | c0007 | t0004 | g0109 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02922 | hp2 | a0002 | c0003 | t0003 | g0110 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02965 | hp1 | a0001 | c0007 | t0004 | g0143 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02965 | hp2 | a0001 | c0005 | t0004 | g0154 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02970 | hp1 | a0004 | c0006 | t0003 | g0010 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02970 | hp2 | a0001 | c0005 | t0004 | g0155 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02976 | hp2 | a0003 | c0004 | t0005 | g0106 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0060 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03041 | hp1 | a0003 | c0004 | t0005 | g0022 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03041 | hp2 | a0001 | c0005 | t0004 | g0149 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03098 | hp1 | a0003 | c0004 | t0005 | g0051 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0112 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03195 | hp2 | a0007 | c0011 | t0004 | g0017 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03209 | hp1 | a0001 | c0005 | t0004 | g0157 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0125 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03225 | hp1 | a0001 | c0005 | t0004 | g0150 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0058 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03453 | hp1 | a0003 | c0004 | t0005 | g0098 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03453 | hp2 | a0001 | c0005 | t0004 | g0161 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03486 | hp1 | a0001 | c0005 | t0004 | g0165 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03486 | hp2 | a0002 | c0003 | t0003 | g0111 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03491 | hp1 | a0002 | c0003 | t0003 | g0121 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03491 | hp2 | a0002 | c0003 | t0003 | g0085 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03516 | hp1 | a0001 | c0007 | t0004 | g0024 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ESN | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03579 | hp1 | a0001 | c0007 | t0004 | g0144 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03579 | hp2 | a0004 | c0006 | t0003 | g0011 | AFR | MSL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03688 | hp1 | a0002 | c0003 | t0003 | g0061 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03710 | hp2 | a0003 | c0004 | t0005 | g0047 | SAS | PJL | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03834 | hp2 | a0008 | c0015 | t0001 | g0172 | SAS | BEB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03942 | hp1 | a0002 | c0003 | t0003 | g0102 | SAS | BEB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG04115 | hp2 | a0002 | c0003 | t0003 | g0116 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG04199 | hp1 | a0002 | c0003 | t0003 | g0062 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18522 | hp2 | a0004 | c0006 | t0003 | g0007 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | CHB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18906 | hp2 | a0001 | c0008 | t0004 | g0141 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0122 | AFR | YRI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA20752 | hp2 | a0003 | c0004 | t0005 | g0036 | EUR | TSI | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0056 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02109 | hp1 | a0001 | c0005 | t0004 | g0162 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02109 | hp2 | a0001 | c0005 | t0004 | g0158 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02486 | hp1 | a0002 | c0003 | t0003 | g0126 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG02486 | hp2 | a0003 | c0004 | t0005 | g0095 | AFR | ACB | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | USA | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| HG06807 | hp2 | a0003 | c0004 | t0005 | g0027 | AFR | USA | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA20300 | hp1 | a0001 | c0005 | t0004 | g0153 | AFR | USA | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA20300 | hp2 | a0001 | c0007 | t0009 | g0142 | AFR | USA | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA21309 | hp1 | a0003 | c0004 | t0005 | g0054 | AFR | LWK | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| NA21309 | hp2 | a0001 | c0005 | t0004 | g0152 | AFR | LWK | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0100 | REF | REF | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | ITGAM_chr16_31254975_31337877 | ITGAM | chr16 | 31254975 | 31337877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31265490
|
G | A | 3 | a0004a0006a0007 | 16 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(13): Show |
missense_variant | MODERATE | c.230G>A | p.Arg77His | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 3/30 | 320/4719 | 230/3459 | 77/1152 | chr16 | 31265490 | ||
| chr16:31277978
|
G | A | 1 | a0010 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1225G>A | p.Ala409Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/30 | 1315/4719 | 1225/3459 | 409/1152 | chr16 | 31277978 | ||
| chr16:31278075
|
T | C | 1 | a0003 | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
missense_variant | MODERATE | c.1322T>C | p.Met441Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/30 | 1412/4719 | 1322/3459 | 441/1152 | chr16 | 31278075 | ||
| chr16:31297854
|
C | T | 1 | a0008 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1607C>T | p.Thr536Met | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/30 | 1697/4719 | 1607/3459 | 536/1152 | chr16 | 31297854 | ||
| chr16:31324464
|
G | A | 1 | a0006 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.2068G>A | p.Val690Ile | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 17/30 | 2158/4719 | 2068/3459 | 690/1152 | chr16 | 31324464 | ||
| chr16:31325567
|
C | T | 2 | a0002a0004 | 38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
missense_variant | MODERATE | c.2573C>T | p.Ala858Val | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/30 | 2663/4719 | 2573/3459 | 858/1152 | chr16 | 31325567 | ||
| chr16:31326927
|
T | A | 1 | a0005 | 2 | HG02040.hp2 HG02129.hp1 |
missense_variant | MODERATE | c.2700T>A | p.Asn900Lys | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/30 | 2790/4719 | 2700/3459 | 900/1152 | chr16 | 31326927 | ||
| chr16:31331663
|
G | A | 1 | a0009 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.3415G>A | p.Asp1139Asn | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 3505/4719 | 3415/3459 | 1139/1152 | chr16 | 31331663 | ||
| chr16:31331684
|
C | T | 2 | a0002a0004 | 38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
missense_variant | MODERATE | c.3436C>T | p.Pro1146Ser | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 3526/4719 | 3436/3459 | 1146/1152 | chr16 | 31331684 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31271969
|
G | A | 1 | a0001c0008 | 2 | HG01891.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.681G>A | p.Thr227Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/30 | 771/4719 | 681/3459 | 227/1152 | chr16 | 31271969 | ||
| chr16:31321334
|
C | T | 3 | a0001c0005a0001c0008a0010c0012 | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
synonymous_variant | LOW | c.1801C>T | p.Leu601Leu | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 15/30 | 1891/4719 | 1801/3459 | 601/1152 | chr16 | 31321334 | ||
| chr16:31321569
|
C | T | 3 | a0001c0007a0006c0010a0007c0011 | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
synonymous_variant | LOW | c.1944C>T | p.Ala648Ala | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/30 | 2034/4719 | 1944/3459 | 648/1152 | chr16 | 31321569 | ||
| chr16:31325398
|
G | A | 2 | a0001c0002a0005c0009 | 59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
synonymous_variant | LOW | c.2499G>A | p.Thr833Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 20/30 | 2589/4719 | 2499/3459 | 833/1152 | chr16 | 31325398 | ||
| chr16:31326873
|
G | A | 1 | a0006c0010 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.2646G>A | p.Thr882Thr | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/30 | 2736/4719 | 2646/3459 | 882/1152 | chr16 | 31326873 | ||
| chr16:31326897
|
C | G | 1 | a0006c0010 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.2670C>G | p.Ser890Ser | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/30 | 2760/4719 | 2670/3459 | 890/1152 | chr16 | 31326897 | ||
| chr16:31328198
|
G | A | 1 | a0001c0013 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.2760G>A | p.Pro920Pro | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/30 | 2850/4719 | 2760/3459 | 920/1152 | chr16 | 31328198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31260027
|
C | T | 1 | a0001c0007t0009 | 1 | NA20300.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/30 | chr16 | 31260027 | ||||||
| chr16:31331860
|
C | CGTGTGTG others(3): Show |
7 | a0001c0001t0002a0001c0002t0002a0001c0002t0007others(4): Show | 94 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*161_*162insGAGTGT others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 162 | INFO_REALIGN_3_PRIME | chr16 | 31331860 | ||||
| chr16:31331894
|
CAT | C | 7 | a0001c0001t0002a0001c0002t0002a0001c0002t0007others(4): Show | 94 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*188_*189delAT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 188 | chr16 | 31331894 | |||||
| chr16:31331914
|
T | C | 2 | a0003c0004t0005a0003c0004t0006 | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*207T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 207 | chr16 | 31331914 | |||||
| chr16:31331922
|
T | C | 17 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(14): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*215T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 215 | chr16 | 31331922 | |||||
| chr16:31332065
|
A | G | 2 | a0002c0003t0003a0004c0006t0003 | 38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*358A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 358 | chr16 | 31332065 | |||||
| chr16:31332332
|
A | G | 17 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(14): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*625A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 625 | chr16 | 31332332 | |||||
| chr16:31332349
|
G | C | 1 | a0001c0002t0007 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 642 | chr16 | 31332349 | |||||
| chr16:31332399
|
G | A | 1 | a0001c0013t0008 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 692 | chr16 | 31332399 | |||||
| chr16:31332448
|
T | C | 17 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(14): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*741T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 741 | chr16 | 31332448 | |||||
| chr16:31332619
|
C | T | 1 | a0003c0004t0006 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*912C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 912 | chr16 | 31332619 | |||||
| chr16:31332634
|
T | TTTTAC | 2 | a0003c0004t0005a0003c0004t0006 | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*928_*932dupTTTAC | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 30/30 | 933 | INFO_REALIGN_3_PRIME | chr16 | 31332634 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:31260224
|
G | A | 141 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(138): Show | 141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.28+132G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260224 | ||||||
| chr16:31260344
|
G | T | 1 | a0001c0005t0004g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28+252G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260344 | ||||||
| chr16:31260379
|
T | C | 25 | a0001c0001t0004g0147a0001c0005t0004g0001a0001c0005t0004g0149others(22): Show | 26 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.28+287T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260379 | ||||||
| chr16:31260549
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.28+457G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260549 | ||||||
| chr16:31260659
|
C | T | 1 | a0001c0007t0009g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.28+567C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260659 | ||||||
| chr16:31260670
|
C | T | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.28+578C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260670 | ||||||
| chr16:31260796
|
C | G | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.28+704C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31260796 | ||||||
| chr16:31261032
|
G | A | 17 | a0002c0003t0003g0016a0004c0006t0003g0002a0004c0006t0003g0003others(14): Show | 17 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.29-660G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261032 | ||||||
| chr16:31261093
|
C | T | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.29-599C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261093 | ||||||
| chr16:31261116
|
G | A | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-576G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261116 | ||||||
| chr16:31261198
|
C | CT | 21 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(18): Show | 21 | HG01106.hp1 HG01358.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.29-472dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261198 | |||||
| chr16:31261198
|
C | CTTT | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-474_29-472dupTT others(1): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261198 | |||||
| chr16:31261198
|
CT | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0167a0001c0001t0001g0169others(10): Show | 13 | HG01256.hp2 HG01496.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-472delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261198 | |||||
| chr16:31261198
|
CTTTTTTT | C | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.29-478_29-472delTT others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261198 | |||||
| chr16:31261221
|
G | C | 1 | a0002c0003t0003g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.29-471G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261221 | ||||||
| chr16:31261342
|
C | T | 3 | a0002c0003t0003g0119a0002c0003t0003g0120a0002c0003t0003g0121 | 3 | HG00741.hp2 HG01106.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.29-350C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | chr16 | 31261342 | ||||||
| chr16:31261513
|
G | GT | 6 | a0001c0001t0001g0118a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 6 | HG02040.hp1 HG03486.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-169dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr16 | 31261513 | |||||
| chr16:31261808
|
T | C | 150 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(147): Show | 151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.134+11T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31261808 | ||||||
| chr16:31262209
|
T | A | 151 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(148): Show | 152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.134+412T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262209 | ||||||
| chr16:31262234
|
C | T | 1 | a0001c0007t0004g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.134+437C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262234 | ||||||
| chr16:31262328
|
C | CTCCCTTC others(2): Show |
7 | a0001c0005t0004g0149a0001c0005t0004g0150a0001c0005t0004g0151others(4): Show | 7 | HG02258.hp2 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.134+539_134+540ins others(9): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262328 | |||||
| chr16:31262330
|
C | CCCTTCCT others(6): Show |
1 | a0001c0005t0004g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.134+539_134+540ins others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262330 | |||||
| chr16:31262330
|
CCCTTCCA others(1): Show |
C | 4 | a0001c0007t0004g0143a0001c0007t0004g0144a0001c0007t0004g0145others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+540_134+547del others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262330 | |||||
| chr16:31262337
|
A | ATCCT | 17 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0228others(14): Show | 17 | HG00544.hp2 HG00609.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.134+603_134+606dup others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | |||||
| chr16:31262337
|
A | T | 24 | a0001c0001t0001g0173a0001c0001t0001g0237a0001c0001t0004g0147others(21): Show | 25 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.134+540A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262337 | ||||||
| chr16:31262337
|
ATCCT | A | 55 | a0001c0001t0001g0064a0001c0001t0001g0075a0001c0001t0001g0166others(52): Show | 55 | HG00558.hp2 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.134+603_134+606del others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | |||||
| chr16:31262337
|
ATCCTTCC others(1): Show |
A | 56 | a0001c0001t0001g0020a0001c0001t0001g0169a0001c0001t0001g0181others(53): Show | 56 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.134+599_134+606del others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | |||||
| chr16:31262337
|
ATCCTTCC others(5): Show |
A | 24 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 24 | HG00323.hp1 HG00673.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.134+595_134+606del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | |||||
| chr16:31262337
|
ATCCTTCC others(9): Show |
A | 7 | a0001c0001t0001g0176a0001c0001t0001g0238a0001c0001t0001g0239others(4): Show | 7 | HG00733.hp2 HG00741.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.134+591_134+606del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | |||||
| chr16:31262337
|
ATCCTTCC others(13): Show |
A | 1 | a0001c0002t0002g0026 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.134+587_134+606del others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | |||||
| chr16:31262337
|
ATCCTTCC others(17): Show |
A | 5 | a0001c0007t0009g0142a0001c0008t0004g0140a0001c0008t0004g0141others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+583_134+606del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | |||||
| chr16:31262337
|
ATCCTTCC others(21): Show |
A | 2 | a0001c0001t0002g0174a0004c0006t0003g0002 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.134+579_134+606del others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262337 | |||||
| chr16:31262341
|
T | A | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134+544T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262341 | ||||||
| chr16:31262345
|
T | A | 7 | a0001c0001t0002g0139a0001c0007t0004g0023a0001c0007t0004g0024others(4): Show | 7 | HG01496.hp2 HG02630.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.134+548T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262345 | ||||||
| chr16:31262349
|
T | A | 16 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(13): Show | 16 | HG00738.hp2 HG01106.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.134+552T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262349 | ||||||
| chr16:31262353
|
T | A | 12 | a0001c0007t0004g0109a0002c0003t0003g0123a0004c0006t0003g0004others(9): Show | 12 | HG00323.hp1 HG00741.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.134+556T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262353 | ||||||
| chr16:31262357
|
T | A | 2 | a0002c0003t0003g0110a0004c0006t0003g0003 | 2 | HG00733.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.134+560T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262357 | ||||||
| chr16:31262365
|
T | A | 4 | a0001c0007t0009g0142a0001c0008t0004g0140a0001c0008t0004g0141others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.134+568T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262365 | ||||||
| chr16:31262369
|
T | A | 2 | a0001c0001t0002g0174a0004c0006t0003g0002 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.134+572T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262369 | ||||||
| chr16:31262390
|
T | G | 18 | a0001c0001t0004g0147a0001c0005t0004g0001a0001c0005t0004g0149others(15): Show | 19 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.134+593T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262390 | ||||||
| chr16:31262390
|
T | TCCTG | 5 | a0001c0005t0004g0159a0001c0005t0004g0160a0001c0005t0004g0161others(2): Show | 5 | HG02109.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.134+596_134+597ins others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262390 | |||||
| chr16:31262390
|
T | TCCTTCCT others(5): Show |
1 | a0001c0005t0004g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.134+604_134+605ins others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262390 | |||||
| chr16:31262390
|
T | TCCTTCCT others(9): Show |
1 | a0010c0012t0004g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.134+606_134+607ins others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31262390 | |||||
| chr16:31262421
|
C | A | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.134+624C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262421 | ||||||
| chr16:31262539
|
ACTACAG | A | 25 | a0001c0001t0004g0147a0001c0005t0004g0001a0001c0005t0004g0149others(22): Show | 26 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.134+743_134+748del others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262539 | ||||||
| chr16:31262560
|
ACCTGGCT others(5): Show |
A | 3 | a0001c0002t0002g0055a0001c0002t0002g0056a0001c0002t0002g0057 | 3 | HG01070.hp1 HG01071.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.134+764_134+775del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262560 | ||||||
| chr16:31262924
|
A | G | 14 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(11): Show | 14 | HG01496.hp2 HG02280.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.134+1127A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31262924 | ||||||
| chr16:31263230
|
C | T | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.134+1433C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263230 | ||||||
| chr16:31263554
|
C | T | 19 | a0002c0003t0003g0016a0002c0003t0003g0119a0002c0003t0003g0120others(16): Show | 19 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.134+1757C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263554 | ||||||
| chr16:31263572
|
T | C | 1 | a0001c0007t0009g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.134+1775T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263572 | ||||||
| chr16:31263608
|
T | A | 14 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(11): Show | 14 | HG01496.hp2 HG02280.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.135-1787T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263608 | ||||||
| chr16:31263665
|
CT | C | 29 | a0001c0001t0001g0193a0001c0001t0001g0237a0001c0001t0004g0147others(26): Show | 30 | HG01516.hp2 HG01517.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.135-1715delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263665 | |||||
| chr16:31263669
|
T | C | 1 | a0001c0002t0002g0026 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.135-1726T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263669 | ||||||
| chr16:31263802
|
A | AATTT | 12 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(9): Show | 12 | HG01516.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.135-1545_135-1542d others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | |||||
| chr16:31263802
|
AATTT | A | 116 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0033others(113): Show | 116 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.135-1545_135-1542d others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | |||||
| chr16:31263802
|
AATTTATT others(1): Show |
A | 36 | a0001c0001t0001g0020a0001c0001t0001g0064a0001c0001t0001g0081others(33): Show | 36 | HG00544.hp1 HG00609.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.135-1549_135-1542d others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | |||||
| chr16:31263802
|
AATTTATT others(5): Show |
A | 9 | a0001c0001t0001g0100a0001c0002t0002g0059a0001c0007t0004g0109others(6): Show | 9 | HG00099.hp1 HG00741.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.135-1553_135-1542d others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | |||||
| chr16:31263802
|
AATTTATT others(9): Show |
A | 27 | a0001c0001t0001g0212a0001c0001t0004g0147a0001c0005t0004g0001others(24): Show | 28 | HG01257.hp2 HG01496.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.135-1557_135-1542d others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | |||||
| chr16:31263802
|
AATTTATT others(13): Show |
A | 1 | a0001c0001t0001g0194 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.135-1561_135-1542d others(22): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31263802 | |||||
| chr16:31263905
|
G | A | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.135-1490G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263905 | ||||||
| chr16:31263993
|
G | A | 2 | a0001c0002t0002g0042a0001c0002t0002g0073 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.135-1402G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31263993 | ||||||
| chr16:31264053
|
T | G | 164 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(161): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.135-1342T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264053 | ||||||
| chr16:31264072
|
G | A | 18 | a0002c0003t0003g0016a0002c0003t0003g0119a0002c0003t0003g0120others(15): Show | 18 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.135-1323G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264072 | ||||||
| chr16:31264085
|
C | T | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.135-1310C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264085 | ||||||
| chr16:31264088
|
G | A | 11 | a0001c0001t0001g0100a0003c0004t0005g0019a0003c0004t0005g0022others(8): Show | 11 | HG00099.hp1 HG01175.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.135-1307G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264088 | ||||||
| chr16:31264302
|
C | T | 25 | a0001c0001t0004g0147a0001c0005t0004g0001a0001c0005t0004g0149others(22): Show | 26 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.135-1093C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264302 | ||||||
| chr16:31264542
|
A | G | 1 | a0002c0003t0003g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.135-853A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264542 | ||||||
| chr16:31264648
|
A | C | 95 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(92): Show | 95 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.135-747A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264648 | ||||||
| chr16:31264749
|
C | T | 1 | a0001c0002t0002g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.135-646C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264749 | ||||||
| chr16:31264750
|
G | A | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.135-645G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31264750 | ||||||
| chr16:31265060
|
G | A | 1 | a0003c0004t0005g0036 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.135-335G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31265060 | ||||||
| chr16:31265160
|
G | A | 25 | a0001c0001t0004g0147a0001c0005t0004g0001a0001c0005t0004g0149others(22): Show | 26 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.135-235G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | chr16 | 31265160 | ||||||
| chr16:31265244
|
AT | A | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.135-144delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr16 | 31265244 | |||||
| chr16:31265570
|
G | A | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.238+72G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 3/29 | chr16 | 31265570 | ||||||
| chr16:31265616
|
C | T | 139 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(136): Show | 139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.238+118C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 3/29 | chr16 | 31265616 | ||||||
| chr16:31265916
|
G | A | 1 | a0001c0002t0002g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.309+35G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 4/29 | chr16 | 31265916 | ||||||
| chr16:31265981
|
C | T | 1 | a0008c0015t0001g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.310-49C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 4/29 | chr16 | 31265981 | ||||||
| chr16:31266219
|
T | C | 1 | a0003c0004t0005g0095 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.427+72T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266219 | ||||||
| chr16:31266417
|
T | TA | 7 | a0001c0001t0001g0181a0001c0001t0001g0195a0001c0001t0001g0196others(4): Show | 7 | HG01175.hp2 HG01243.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+290dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266417 | |||||
| chr16:31266417
|
TA | T | 154 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0033others(151): Show | 155 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.427+290delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266417 | |||||
| chr16:31266417
|
TAA | T | 6 | a0001c0001t0001g0020a0001c0001t0002g0134a0001c0002t0002g0057others(3): Show | 6 | HG01070.hp1 HG02809.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+289_427+290del others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266417 | |||||
| chr16:31266417
|
TAAA | T | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+288_427+290del others(3): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266417 | |||||
| chr16:31266558
|
C | CA | 30 | a0001c0001t0001g0214a0001c0001t0004g0114a0001c0001t0004g0115others(27): Show | 31 | HG00741.hp1 HG01106.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.427+426dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266558 | |||||
| chr16:31266616
|
A | C | 1 | a0001c0001t0001g0224 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.427+469A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266616 | ||||||
| chr16:31266738
|
A | G | 2 | a0002c0003t0003g0112a0002c0003t0003g0113 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.427+591A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266738 | ||||||
| chr16:31266741
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.427+594A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266741 | ||||||
| chr16:31266862
|
A | AT | 10 | a0001c0001t0001g0179a0001c0001t0001g0189a0001c0001t0001g0190others(7): Show | 10 | HG02055.hp1 HG02451.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.427+738dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266862 | |||||
| chr16:31266862
|
AT | A | 8 | a0001c0001t0001g0170a0001c0001t0004g0147a0001c0007t0004g0143others(5): Show | 8 | HG01070.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.427+738delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266862 | |||||
| chr16:31266862
|
ATTTTTTT others(4): Show |
A | 1 | a0004c0006t0003g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+728_427+738del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266862 | |||||
| chr16:31266862
|
ATTTTTTT others(5): Show |
A | 158 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(155): Show | 159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.427+727_427+738del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31266862 | |||||
| chr16:31266970
|
C | T | 1 | a0004c0006t0003g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.427+823C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31266970 | ||||||
| chr16:31267216
|
C | G | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+1069C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267216 | ||||||
| chr16:31267435
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0210 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.427+1288C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267435 | ||||||
| chr16:31267491
|
G | A | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.427+1344G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267491 | ||||||
| chr16:31267507
|
C | G | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+1360C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267507 | ||||||
| chr16:31267670
|
G | T | 167 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(164): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.427+1523G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267670 | ||||||
| chr16:31267911
|
T | G | 2 | a0004c0006t0003g0005a0004c0006t0003g0006 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.427+1764T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31267911 | ||||||
| chr16:31268124
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.427+1977C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268124 | ||||||
| chr16:31268127
|
C | A | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+1980C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268127 | ||||||
| chr16:31268215
|
T | C | 145 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(142): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.427+2068T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268215 | ||||||
| chr16:31268528
|
G | A | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+2381G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268528 | ||||||
| chr16:31268756
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428-2198C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268756 | ||||||
| chr16:31268791
|
C | A | 5 | a0001c0005t0004g0156a0001c0005t0004g0157a0001c0005t0004g0158others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-2163C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268791 | ||||||
| chr16:31268934
|
G | A | 160 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(157): Show | 161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.428-2020G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268934 | ||||||
| chr16:31268936
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0118a0001c0002t0002g0041 | 3 | HG02083.hp2 NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.428-2018C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268936 | ||||||
| chr16:31268961
|
G | A | 160 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(157): Show | 161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.428-1993G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31268961 | ||||||
| chr16:31269081
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.428-1873C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269081 | ||||||
| chr16:31269127
|
T | C | 1 | a0001c0007t0004g0143 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.428-1827T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269127 | ||||||
| chr16:31269131
|
C | T | 1 | a0001c0007t0004g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.428-1823C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269131 | ||||||
| chr16:31269188
|
C | T | 1 | a0001c0005t0004g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.428-1766C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269188 | ||||||
| chr16:31269340
|
T | C | 160 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(157): Show | 161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.428-1614T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269340 | ||||||
| chr16:31269349
|
T | C | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.428-1605T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269349 | ||||||
| chr16:31269412
|
G | A | 1 | a0007c0011t0004g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.428-1542G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269412 | ||||||
| chr16:31269599
|
A | T | 1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.428-1355A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269599 | ||||||
| chr16:31269826
|
A | G | 96 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(93): Show | 96 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.428-1128A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269826 | ||||||
| chr16:31269849
|
G | A | 8 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0001g0198others(5): Show | 8 | HG01243.hp2 HG01257.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-1105G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31269849 | ||||||
| chr16:31270084
|
CCTT | C | 49 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(46): Show | 49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.428-869_428-867del others(3): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270084 | ||||||
| chr16:31270103
|
A | ATCCT | 5 | a0001c0001t0001g0194a0001c0005t0004g0152a0001c0005t0004g0157others(2): Show | 5 | HG02165.hp1 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-826_428-823dup others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270103 | |||||
| chr16:31270103
|
A | ATCCTTCC others(5): Show |
1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.428-834_428-823dup others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270103 | |||||
| chr16:31270103
|
A | ATCCTTCC others(9): Show |
4 | a0001c0007t0004g0143a0001c0007t0004g0144a0001c0007t0004g0145others(1): Show | 4 | HG02647.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-838_428-823dup others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270103 | |||||
| chr16:31270103
|
A | ATCCTTCC others(13): Show |
1 | a0001c0007t0004g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.428-842_428-823dup others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270103 | |||||
| chr16:31270126
|
C | CTCCTTTG others(7): Show |
2 | a0001c0008t0004g0140a0007c0011t0004g0017 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.428-827_428-826ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(12): Show |
2 | a0001c0007t0004g0023a0001c0007t0009g0142 | 2 | HG01496.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.428-827_428-826ins others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(17): Show |
3 | a0001c0007t0004g0109a0002c0003t0003g0126a0002c0003t0003g0127 | 3 | HG01891.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.428-827_428-826ins others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(22): Show |
3 | a0001c0007t0004g0024a0004c0006t0003g0009a0006c0010t0004g0018 | 3 | HG02895.hp1 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.428-827_428-826ins others(29): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(27): Show |
5 | a0002c0003t0003g0016a0002c0003t0003g0123a0004c0006t0003g0003others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-827_428-826ins others(34): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(32): Show |
7 | a0002c0003t0003g0122a0002c0003t0003g0124a0002c0003t0003g0125others(4): Show | 7 | HG00323.hp1 HG00738.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-827_428-826ins others(39): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(37): Show |
5 | a0002c0003t0003g0061a0002c0003t0003g0062a0002c0003t0003g0116others(2): Show | 5 | HG03579.hp2 HG03688.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-827_428-826ins others(44): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(42): Show |
4 | a0002c0003t0003g0080a0002c0003t0003g0102a0004c0006t0003g0004others(1): Show | 4 | HG00741.hp1 HG01516.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-827_428-826ins others(49): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(47): Show |
3 | a0002c0003t0003g0060a0004c0006t0003g0005a0004c0006t0003g0006 | 3 | HG01256.hp1 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.428-827_428-826ins others(54): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270126
|
C | CTCCTTTG others(57): Show |
1 | a0002c0003t0003g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.428-827_428-826ins others(64): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270126 | |||||
| chr16:31270130
|
C | CTT | 36 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(33): Show | 36 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.428-823_428-822ins others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270130
|
C | CTTCCTCC others(7): Show |
8 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0220others(5): Show | 8 | HG00099.hp2 HG01123.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-823_428-822ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270130
|
C | CTTCCTCC others(12): Show |
8 | a0001c0001t0001g0208a0001c0001t0001g0224a0001c0005t0004g0001others(5): Show | 9 | HG00642.hp1 HG02258.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.428-823_428-822ins others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270130
|
C | CTTCCTCC others(17): Show |
1 | a0001c0005t0004g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.428-823_428-822ins others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270130
|
C | CTTCCTCC others(22): Show |
3 | a0001c0005t0004g0149a0001c0005t0004g0162a0010c0012t0004g0164 | 3 | HG02109.hp1 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.428-823_428-822ins others(29): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270130
|
C | CTTCCTTC others(11): Show |
1 | a0001c0005t0004g0160 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.428-823_428-822ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270130
|
C | CTTCCTTC others(16): Show |
1 | a0001c0005t0004g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.428-823_428-822ins others(23): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270130
|
C | CTTCCTTC others(47): Show |
1 | a0001c0001t0004g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.428-823_428-822ins others(54): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270130
|
C | CTTCCTTC others(52): Show |
1 | a0001c0001t0004g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.428-823_428-822ins others(59): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270130 | |||||
| chr16:31270137
|
G | C | 60 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0208others(57): Show | 61 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.428-817G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270137 | ||||||
| chr16:31270137
|
G | GCTTTC | 9 | a0001c0001t0001g0100a0001c0001t0001g0187a0001c0001t0001g0193others(6): Show | 9 | HG02015.hp2 HG02165.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.428-767_428-763dup others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | |||||
| chr16:31270137
|
G | GCTTTCCT others(3): Show |
29 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0166others(26): Show | 29 | HG00544.hp2 HG00609.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.428-772_428-763dup others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | |||||
| chr16:31270137
|
G | GCTTTCCT others(8): Show |
21 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0189others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.428-777_428-763dup others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | |||||
| chr16:31270137
|
G | GCTTTCCT others(13): Show |
1 | a0001c0002t0002g0229 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.428-782_428-763dup others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | |||||
| chr16:31270137
|
G | GCTTTCCT others(18): Show |
2 | a0001c0001t0001g0181a0001c0001t0001g0216 | 2 | HG01243.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.428-787_428-763dup others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | |||||
| chr16:31270137
|
GCTTTCCT others(3): Show |
G | 3 | a0001c0001t0001g0170a0001c0001t0001g0235a0001c0002t0002g0211 | 3 | NA18945.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.428-772_428-763del others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | |||||
| chr16:31270137
|
GCTTTCCT others(18): Show |
G | 12 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(9): Show | 12 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.428-787_428-763del others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | |||||
| chr16:31270137
|
GCTTTCCT others(23): Show |
G | 1 | a0002c0003t0003g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.428-792_428-763del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270137 | |||||
| chr16:31270160
|
TTCCTTTC | T | 88 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(85): Show | 88 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.428-793_428-787del others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270160 | ||||||
| chr16:31270167
|
C | CCTT | 7 | a0001c0001t0002g0174a0001c0001t0004g0147a0001c0007t0004g0143others(4): Show | 7 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-786_428-784dup others(3): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270167 | |||||
| chr16:31270216
|
C | T | 88 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(85): Show | 88 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.428-738C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270216 | ||||||
| chr16:31270217
|
G | A | 2 | a0001c0007t0004g0023a0001c0007t0004g0109 | 2 | HG01496.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428-737G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270217 | ||||||
| chr16:31270393
|
C | T | 13 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(10): Show | 13 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.428-561C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270393 | ||||||
| chr16:31270430
|
T | C | 166 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(163): Show | 167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.428-524T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270430 | ||||||
| chr16:31270688
|
C | CGT | 19 | a0001c0001t0001g0033a0001c0001t0001g0118a0001c0001t0001g0171others(16): Show | 19 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.428-255_428-254dup others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270688 | |||||
| chr16:31270699
|
G | GTA | 5 | a0001c0001t0001g0100a0001c0001t0001g0209a0001c0001t0001g0214others(2): Show | 5 | HG00733.hp2 HG03669.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-211_428-210dup others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTATA | 9 | a0001c0001t0001g0177a0002c0003t0003g0060a0002c0003t0003g0123others(6): Show | 9 | HG00738.hp2 HG01070.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.428-213_428-210dup others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTATATA | 7 | a0001c0001t0001g0223a0001c0007t0004g0023a0002c0003t0003g0124others(4): Show | 7 | HG01106.hp1 HG01109.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-215_428-210dup others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTATATAT others(1): Show |
6 | a0001c0001t0001g0233a0002c0003t0003g0085a0002c0003t0003g0122others(3): Show | 6 | HG00323.hp1 HG01258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-217_428-210dup others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTATATAT others(3): Show |
1 | a0004c0006t0003g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.428-219_428-210dup others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTA | 19 | a0001c0001t0001g0075a0001c0001t0001g0203a0001c0001t0001g0208others(16): Show | 19 | HG00609.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTATA | 25 | a0001c0001t0001g0032a0001c0001t0001g0081a0001c0001t0001g0170others(22): Show | 25 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTATAT others(1): Show |
17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0189others(14): Show | 17 | HG01243.hp2 HG01257.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTATAT others(3): Show |
9 | a0001c0001t0001g0020a0001c0001t0001g0064a0001c0001t0001g0103others(6): Show | 9 | HG01123.hp1 HG03239.hp2 HG04115.hp1 others(6): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTATAT others(5): Show |
5 | a0001c0001t0001g0217a0001c0002t0002g0043a0001c0002t0002g0063others(2): Show | 5 | HG00642.hp2 HG01361.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTATAT others(7): Show |
5 | a0001c0001t0001g0028a0001c0001t0001g0167a0001c0001t0001g0190others(2): Show | 5 | HG00558.hp1 HG01934.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0084 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.428-254_428-253ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTATAT others(23): Show |
2 | a0001c0002t0002g0055a0001c0002t0002g0057 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.428-254_428-253ins others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTAT others(3): Show |
6 | a0001c0001t0001g0195a0001c0001t0001g0240a0001c0001t0002g0131others(3): Show | 6 | HG01358.hp2 HG01952.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTAT others(5): Show |
6 | a0001c0001t0002g0132a0001c0001t0002g0135a0001c0001t0002g0136others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTAT others(7): Show |
4 | a0001c0001t0002g0137a0001c0001t0002g0138a0001c0002t0002g0192others(1): Show | 4 | HG02615.hp1 HG03453.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-254_428-253ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTAT others(9): Show |
3 | a0001c0002t0002g0083a0001c0005t0004g0157a0002c0003t0003g0113 | 3 | HG02523.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.428-254_428-253ins others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTAT others(11): Show |
2 | a0001c0005t0004g0151a0001c0005t0004g0158 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.428-254_428-253ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTAT others(13): Show |
1 | a0001c0001t0002g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.428-254_428-253ins others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTGT others(3): Show |
1 | a0001c0007t0004g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.428-254_428-253ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0169 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.428-254_428-253ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTGT others(9): Show |
1 | a0001c0007t0004g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.428-254_428-253ins others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTGT others(11): Show |
2 | a0001c0002t0002g0168a0001c0007t0004g0146 | 2 | HG02809.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.428-254_428-253ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
G | GTGTGTGT others(15): Show |
2 | a0001c0007t0004g0143a0001c0007t0004g0148 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.428-254_428-253ins others(22): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTA | G | 13 | a0001c0001t0001g0166a0001c0001t0001g0196a0001c0001t0001g0222others(10): Show | 14 | HG01175.hp2 HG01361.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-211_428-210del others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATA | G | 7 | a0001c0001t0001g0173a0001c0001t0001g0187a0001c0001t0001g0193others(4): Show | 7 | HG00544.hp2 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-213_428-210del others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATA | G | 4 | a0001c0001t0001g0185a0001c0001t0001g0232a0001c0002t0002g0021others(1): Show | 4 | HG00609.hp2 HG02273.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-215_428-210del others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATAT others(1): Show |
G | 6 | a0001c0001t0001g0210a0001c0002t0002g0049a0001c0002t0002g0108others(3): Show | 6 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-217_428-210del others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATAT others(3): Show |
G | 2 | a0001c0005t0004g0162a0001c0007t0009g0142 | 2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.428-219_428-210del others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATAT others(5): Show |
G | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428-221_428-210del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATAT others(7): Show |
G | 3 | a0001c0001t0001g0219a0005c0009t0002g0050a0005c0009t0002g0093 | 3 | HG02040.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.428-223_428-210del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0176 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.428-225_428-210del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATAT others(13): Show |
G | 1 | a0004c0006t0003g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.428-229_428-210del others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATAT others(17): Show |
G | 2 | a0001c0002t0002g0072a0001c0002t0002g0082 | 2 | NA18747.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.428-233_428-210del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270699
|
GTATATAT others(23): Show |
G | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.428-239_428-210del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270699 | |||||
| chr16:31270701
|
A | G | 32 | a0001c0001t0001g0178a0001c0001t0001g0207a0001c0001t0001g0234others(29): Show | 32 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.428-253A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270701 | ||||||
| chr16:31270703
|
A | G | 11 | a0001c0001t0001g0166a0001c0001t0001g0196a0001c0001t0001g0222others(8): Show | 12 | HG00099.hp1 HG01175.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.428-251A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270703 | ||||||
| chr16:31270705
|
A | G | 12 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0196others(9): Show | 13 | HG00544.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.428-249A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270705 | ||||||
| chr16:31270706
|
TATATATA others(50): Show |
T | 2 | a0002c0003t0003g0061a0002c0003t0003g0116 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.428-234_428-178del others(57): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270706 | |||||
| chr16:31270707
|
A | G | 4 | a0001c0001t0001g0185a0001c0001t0001g0232a0001c0002t0002g0021others(1): Show | 4 | HG00609.hp2 HG02273.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-247A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270707 | ||||||
| chr16:31270709
|
A | G | 6 | a0001c0001t0001g0210a0001c0002t0002g0049a0001c0002t0002g0108others(3): Show | 6 | HG02055.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-245A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270709 | ||||||
| chr16:31270711
|
A | G | 3 | a0001c0005t0004g0162a0001c0005t0004g0163a0010c0012t0004g0164 | 3 | HG02109.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.428-243A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270711 | ||||||
| chr16:31270713
|
A | G | 3 | a0001c0001t0002g0174a0001c0005t0004g0162a0001c0013t0008g0175 | 3 | HG02109.hp1 HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428-241A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270713 | ||||||
| chr16:31270715
|
A | G | 5 | a0001c0001t0001g0219a0001c0001t0002g0174a0001c0013t0008g0175others(2): Show | 5 | HG02040.hp2 HG02129.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-239A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270715 | ||||||
| chr16:31270717
|
A | G | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428-237A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270717 | ||||||
| chr16:31270719
|
A | G | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.428-235A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270719 | ||||||
| chr16:31270721
|
A | G | 2 | a0001c0001t0002g0174a0004c0006t0003g0010 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.428-233A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270721 | ||||||
| chr16:31270725
|
A | G | 2 | a0001c0002t0002g0072a0001c0002t0002g0082 | 2 | NA18747.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.428-229A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270725 | ||||||
| chr16:31270727
|
A | T | 1 | a0001c0002t0002g0094 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.428-227A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270727 | ||||||
| chr16:31270731
|
A | G | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.428-223A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270731 | ||||||
| chr16:31270734
|
TATATATA others(4): Show |
T | 1 | a0003c0004t0005g0077 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.428-219_428-209del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270734 | ||||||
| chr16:31270741
|
A | T | 1 | a0003c0004t0005g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.428-213A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270741 | ||||||
| chr16:31270742
|
T | TA | 19 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(16): Show | 19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.428-211dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270742 | |||||
| chr16:31270743
|
A | T | 3 | a0003c0004t0005g0051a0003c0004t0005g0078a0003c0004t0005g0079 | 3 | HG00099.hp1 HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.428-211A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270743 | ||||||
| chr16:31270744
|
T | TA | 3 | a0003c0004t0005g0022a0003c0004t0005g0031a0003c0004t0005g0095 | 3 | HG02486.hp2 HG02735.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.428-210_428-209ins others(1): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270744 | ||||||
| chr16:31270744
|
T | TATATATA others(4): Show |
1 | a0003c0004t0005g0025 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.428-210_428-209ins others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270744 | ||||||
| chr16:31270744
|
TG | T | 4 | a0003c0004t0005g0054a0003c0004t0005g0086a0003c0004t0005g0097others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-209delG | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270744 | ||||||
| chr16:31270745
|
G | T | 16 | a0003c0004t0005g0022a0003c0004t0005g0025a0003c0004t0005g0027others(13): Show | 16 | HG00099.hp1 HG01109.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.428-209G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270745 | ||||||
| chr16:31270754
|
G | A | 1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.428-200G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270754 | ||||||
| chr16:31270763
|
CAT | C | 14 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(11): Show | 14 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.428-179_428-178del others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr16 | 31270763 | |||||
| chr16:31270777
|
C | T | 58 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.428-177C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 5/29 | chr16 | 31270777 | ||||||
| chr16:31271392
|
T | G | 166 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(163): Show | 167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.558+308T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271392 | ||||||
| chr16:31271498
|
G | A | 19 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(16): Show | 19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.559-349G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271498 | ||||||
| chr16:31271573
|
A | G | 19 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(16): Show | 19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.559-274A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271573 | ||||||
| chr16:31271649
|
G | A | 35 | a0001c0007t0004g0024a0001c0007t0004g0109a0001c0007t0009g0142others(32): Show | 35 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.559-198G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271649 | ||||||
| chr16:31271659
|
C | T | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.559-188C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271659 | ||||||
| chr16:31271843
|
G | A | 40 | a0001c0001t0002g0174a0001c0001t0004g0114a0001c0001t0004g0115others(37): Show | 40 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(37): Show |
splice_region_variant&intron_variant | LOW | c.559-4G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 6/29 | chr16 | 31271843 | ||||||
| chr16:31272002
|
C | G | 28 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(25): Show | 28 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.704+10C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272002 | ||||||
| chr16:31272151
|
T | C | 45 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(42): Show | 46 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(43): Show |
intron_variant | MODIFIER | c.704+159T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272151 | ||||||
| chr16:31272233
|
A | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0210 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.704+241A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272233 | ||||||
| chr16:31272255
|
T | C | 101 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(98): Show | 102 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(99): Show |
intron_variant | MODIFIER | c.704+263T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272255 | ||||||
| chr16:31272423
|
C | CCATATAT others(3): Show |
1 | a0001c0002t0002g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.704+431_704+432ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272423 | ||||||
| chr16:31272423
|
C | CTATA | 3 | a0001c0001t0001g0202a0001c0001t0001g0217a0001c0002t0002g0041 | 3 | HG00673.hp2 HG02083.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.704+469_704+472dup others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | |||||
| chr16:31272423
|
C | G | 76 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(73): Show | 77 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.704+431C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272423 | ||||||
| chr16:31272423
|
CTA | C | 5 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0240others(2): Show | 5 | HG01358.hp2 HG02055.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+471_704+472del others(2): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | |||||
| chr16:31272423
|
CTATA | C | 14 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0184others(11): Show | 14 | HG01071.hp1 HG01257.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.704+469_704+472del others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | |||||
| chr16:31272423
|
CTATATAT others(1): Show |
C | 3 | a0001c0001t0001g0178a0001c0001t0001g0187a0001c0001t0001g0221 | 3 | HG01123.hp2 HG01255.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.704+465_704+472del others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | |||||
| chr16:31272423
|
CTATATAT others(7): Show |
C | 2 | a0001c0001t0001g0032a0001c0001t0001g0209 | 2 | HG01192.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.704+459_704+472del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | |||||
| chr16:31272423
|
CTATATAT others(9): Show |
C | 1 | a0001c0001t0001g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.704+457_704+472del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | |||||
| chr16:31272423
|
CTATATAT others(11): Show |
C | 1 | a0001c0001t0001g0238 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.704+455_704+472del others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | |||||
| chr16:31272423
|
CTATATAT others(17): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.704+449_704+472del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272423 | |||||
| chr16:31272424
|
T | C | 1 | a0001c0002t0002g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.704+432T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272424 | ||||||
| chr16:31272433
|
ATATATAT others(32): Show |
A | 1 | a0001c0002t0002g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.704+443_704+481del others(39): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272433 | |||||
| chr16:31272435
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.704+445_704+475del others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272435 | |||||
| chr16:31272436
|
TATATATA others(18): Show |
T | 1 | a0001c0001t0001g0214 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.704+445_704+469del others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272436 | ||||||
| chr16:31272437
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0205 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.704+447_704+474del others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272437 | |||||
| chr16:31272440
|
TATATATA others(14): Show |
T | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.704+449_704+469del others(21): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272440 | ||||||
| chr16:31272441
|
ATATATAT others(35): Show |
A | 3 | a0001c0005t0004g0154a0001c0005t0004g0158a0001c0005t0004g0161 | 3 | HG02109.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.704+451_704+492del others(42): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272441 | |||||
| chr16:31272441
|
ATATATAT others(36): Show |
A | 3 | a0001c0005t0004g0156a0001c0005t0004g0157a0001c0005t0004g0159 | 3 | HG02145.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.704+451_704+493del others(43): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272441 | |||||
| chr16:31272442
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0216 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.704+451_704+469del others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272442 | ||||||
| chr16:31272443
|
ATATATAT others(20): Show |
A | 1 | a0002c0003t0003g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.704+453_704+479del others(27): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | |||||
| chr16:31272443
|
ATATATAT others(22): Show |
A | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.704+453_704+481del others(29): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | |||||
| chr16:31272443
|
ATATATAT others(23): Show |
A | 6 | a0003c0004t0005g0025a0003c0004t0005g0027a0003c0004t0005g0077others(3): Show | 6 | HG01109.hp2 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.704+453_704+482del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | |||||
| chr16:31272443
|
ATATATAT others(24): Show |
A | 1 | a0003c0004t0005g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.704+453_704+483del others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | |||||
| chr16:31272443
|
ATATATAT others(35): Show |
A | 12 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0151others(9): Show | 13 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.704+453_704+494del others(42): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272443 | |||||
| chr16:31272445
|
ATATATAT others(17): Show |
A | 1 | a0001c0002t0002g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.704+455_704+478del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | |||||
| chr16:31272445
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0004g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704+455_704+481del others(27): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | |||||
| chr16:31272445
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0004g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.704+455_704+482del others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | |||||
| chr16:31272445
|
ATATATAT others(22): Show |
A | 2 | a0003c0004t0005g0037a0003c0004t0005g0096 | 2 | HG01175.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.704+455_704+483del others(29): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | |||||
| chr16:31272445
|
ATATATAT others(23): Show |
A | 7 | a0003c0004t0005g0036a0003c0004t0005g0047a0003c0004t0005g0051others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+455_704+484del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | |||||
| chr16:31272445
|
ATATATAT others(24): Show |
A | 2 | a0003c0004t0005g0019a0003c0004t0005g0105 | 2 | HG01256.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.704+455_704+485del others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | |||||
| chr16:31272445
|
ATATATAT others(30): Show |
A | 1 | a0003c0004t0005g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.704+455_704+491del others(37): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | |||||
| chr16:31272445
|
ATATATAT others(35): Show |
A | 1 | a0001c0005t0004g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.704+455_704+496del others(42): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272445 | |||||
| chr16:31272447
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0002g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.704+457_704+476del others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | |||||
| chr16:31272447
|
ATATATAT others(17): Show |
A | 1 | a0004c0006t0003g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.704+457_704+480del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | |||||
| chr16:31272447
|
ATATATAT others(18): Show |
A | 1 | a0007c0011t0004g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.704+457_704+481del others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | |||||
| chr16:31272447
|
ATATATAT others(19): Show |
A | 2 | a0002c0003t0003g0125a0002c0003t0003g0127 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.704+457_704+482del others(26): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | |||||
| chr16:31272447
|
ATATATAT others(21): Show |
A | 1 | a0003c0004t0005g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.704+457_704+484del others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | |||||
| chr16:31272447
|
ATATATAT others(23): Show |
A | 2 | a0003c0004t0005g0078a0003c0004t0005g0086 | 2 | HG01255.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.704+457_704+486del others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | |||||
| chr16:31272447
|
ATATATAT others(24): Show |
A | 1 | a0003c0004t0005g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.704+457_704+487del others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272447 | |||||
| chr16:31272449
|
ATATATAT others(9): Show |
A | 1 | a0001c0007t0004g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.704+459_704+474del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272449 | |||||
| chr16:31272449
|
ATATATAT others(17): Show |
A | 5 | a0002c0003t0003g0102a0004c0006t0003g0005a0004c0006t0003g0006others(2): Show | 5 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+459_704+482del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272449 | |||||
| chr16:31272449
|
ATATATAT others(19): Show |
A | 2 | a0002c0003t0003g0124a0002c0003t0003g0126 | 2 | HG01106.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.704+459_704+484del others(26): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272449 | |||||
| chr16:31272450
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0193 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.704+459_704+469del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272450 | ||||||
| chr16:31272451
|
ATATATAT others(7): Show |
A | 1 | a0002c0003t0003g0111 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704+461_704+474del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(10): Show |
A | 2 | a0001c0002t0002g0094a0001c0007t0004g0109 | 2 | HG02080.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.704+461_704+477del others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0081 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.704+461_704+478del others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(12): Show |
A | 1 | a0001c0002t0002g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.704+461_704+479del others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(13): Show |
A | 1 | a0001c0002t0002g0071 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.704+461_704+480del others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(15): Show |
A | 3 | a0002c0003t0003g0080a0002c0003t0003g0116a0004c0006t0003g0004 | 3 | HG00741.hp1 HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.704+461_704+482del others(22): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(16): Show |
A | 1 | a0002c0003t0003g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.704+461_704+483del others(23): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(17): Show |
A | 6 | a0002c0003t0003g0060a0002c0003t0003g0062a0002c0003t0003g0085others(3): Show | 6 | HG00733.hp2 HG01109.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.704+461_704+484del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(18): Show |
A | 4 | a0001c0007t0009g0142a0002c0003t0003g0123a0004c0006t0003g0007others(1): Show | 4 | HG00738.hp2 HG02622.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+461_704+485del others(25): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272451
|
ATATATAT others(19): Show |
A | 4 | a0002c0003t0003g0016a0002c0003t0003g0122a0004c0006t0003g0010others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+461_704+486del others(26): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272451 | |||||
| chr16:31272453
|
ATATATAT others(10): Show |
A | 7 | a0001c0002t0002g0035a0001c0002t0002g0043a0001c0002t0002g0052others(4): Show | 7 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.704+463_704+479del others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | |||||
| chr16:31272453
|
ATATATAT others(11): Show |
A | 1 | a0001c0002t0002g0040 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.704+463_704+480del others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | |||||
| chr16:31272453
|
ATATATAT others(14): Show |
A | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.704+463_704+483del others(21): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | |||||
| chr16:31272453
|
ATATATAT others(17): Show |
A | 1 | a0004c0006t0003g0008 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.704+463_704+486del others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | |||||
| chr16:31272453
|
ATATATAT others(26): Show |
A | 1 | a0001c0001t0001g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.704+463_704+495del others(33): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272453 | |||||
| chr16:31272454
|
TATATA | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0223a0001c0002t0002g0215 | 3 | HG02129.hp2 HG03669.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.704+463_704+467del others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272454 | ||||||
| chr16:31272455
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.704+463A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272455 | ||||||
| chr16:31272455
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0002g0174a0001c0007t0004g0144 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.704+465_704+476del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | |||||
| chr16:31272455
|
ATATATAT others(6): Show |
A | 1 | a0001c0007t0004g0143 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.704+465_704+477del others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | |||||
| chr16:31272455
|
ATATATAT others(9): Show |
A | 2 | a0001c0002t0002g0063a0001c0002t0002g0066 | 2 | HG01257.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.704+465_704+480del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | |||||
| chr16:31272455
|
ATATATAT others(10): Show |
A | 1 | a0001c0002t0002g0065 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.704+465_704+481del others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | |||||
| chr16:31272455
|
ATATATAT others(11): Show |
A | 2 | a0001c0001t0001g0103a0001c0001t0001g0222 | 2 | HG02738.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.704+465_704+482del others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272455 | |||||
| chr16:31272457
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0233 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.704+466_704+467ins others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272457 | |||||
| chr16:31272457
|
A | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0209 | 2 | HG01952.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.704+465A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272457 | ||||||
| chr16:31272457
|
ATATATAT others(4): Show |
A | 1 | a0001c0002t0007g0030 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.704+467_704+477del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272457 | |||||
| chr16:31272457
|
ATATATAT others(6): Show |
A | 4 | a0001c0007t0004g0145a0001c0007t0004g0148a0001c0013t0008g0175others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+467_704+479del others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272457 | |||||
| chr16:31272457
|
ATATATAT others(7): Show |
A | 2 | a0001c0002t0002g0045a0001c0002t0002g0070 | 2 | HG01358.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.704+467_704+480del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272457 | |||||
| chr16:31272459
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0176 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.704+468_704+469ins others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | |||||
| chr16:31272459
|
A | ATTTTTTT others(12): Show |
1 | a0009c0014t0001g0225 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.704+468_704+469ins others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | |||||
| chr16:31272459
|
A | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0195a0001c0001t0001g0196others(4): Show | 7 | HG00558.hp2 HG00642.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+467A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272459 | ||||||
| chr16:31272459
|
ATATATTT others(4): Show |
A | 1 | a0002c0003t0003g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.704+469_704+479del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | |||||
| chr16:31272459
|
ATATATTT others(6): Show |
A | 3 | a0001c0002t0002g0026a0001c0002t0002g0067a0001c0007t0004g0146 | 3 | HG02809.hp2 NA19063.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.704+469_704+481del others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | |||||
| chr16:31272459
|
ATATATTT others(8): Show |
A | 2 | a0001c0002t0002g0229a0002c0003t0003g0113 | 2 | HG02630.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.704+469_704+483del others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272459 | |||||
| chr16:31272461
|
A | T | 17 | a0001c0001t0001g0032a0001c0001t0001g0170a0001c0001t0001g0176others(14): Show | 17 | HG00558.hp2 HG00642.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.704+469A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272461 | ||||||
| chr16:31272461
|
ATATTTTT others(4): Show |
A | 1 | a0001c0002t0002g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.704+471_704+481del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272461 | |||||
| chr16:31272461
|
ATATTTTT others(7): Show |
A | 1 | a0001c0001t0002g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.704+471_704+484del others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272461 | |||||
| chr16:31272463
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.704+472_704+473ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | |||||
| chr16:31272463
|
A | ATATATTT others(10): Show |
1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.704+472_704+473ins others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | |||||
| chr16:31272463
|
A | T | 36 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0170others(33): Show | 36 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.704+471A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272463 | ||||||
| chr16:31272463
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0002g0131a0001c0002t0002g0180 | 2 | HG02723.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.704+500_704+509del others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | |||||
| chr16:31272463
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0020 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.704+499_704+509del others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | |||||
| chr16:31272463
|
ATTTTTTT others(5): Show |
A | 7 | a0001c0001t0001g0177a0001c0001t0001g0237a0001c0001t0002g0132others(4): Show | 7 | HG01516.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.704+498_704+509del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | |||||
| chr16:31272463
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0173 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.704+497_704+509del others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | |||||
| chr16:31272463
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0007t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.704+494_704+509del others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31272463 | |||||
| chr16:31272464
|
T | TATATATA | 3 | a0001c0002t0002g0044a0001c0002t0002g0104a0005c0009t0002g0093 | 3 | HG02040.hp2 NA18963.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.704+472_704+473ins others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272464 | ||||||
| chr16:31272464
|
T | TATATATA others(6): Show |
2 | a0001c0002t0002g0087a0005c0009t0002g0050 | 2 | HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.704+472_704+473ins others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272464 | ||||||
| chr16:31272465
|
T | A | 7 | a0001c0001t0001g0084a0001c0002t0002g0041a0001c0002t0002g0046others(4): Show | 7 | HG02015.hp1 HG02071.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+473T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272465 | ||||||
| chr16:31272466
|
T | A | 7 | a0001c0002t0002g0029a0001c0002t0002g0042a0001c0002t0002g0044others(4): Show | 7 | HG00558.hp1 HG00673.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+474T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272466 | ||||||
| chr16:31272467
|
T | A | 6 | a0001c0001t0001g0084a0001c0002t0002g0041a0001c0002t0002g0046others(3): Show | 6 | HG02015.hp1 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.704+475T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272467 | ||||||
| chr16:31272468
|
T | A | 8 | a0001c0001t0001g0181a0001c0002t0002g0029a0001c0002t0002g0042others(5): Show | 8 | HG00558.hp1 HG00673.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.704+476T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272468 | ||||||
| chr16:31272469
|
T | A | 7 | a0001c0001t0001g0084a0001c0002t0002g0041a0001c0002t0002g0046others(4): Show | 7 | HG02015.hp1 HG02056.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+477T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272469 | ||||||
| chr16:31272470
|
T | A | 9 | a0001c0001t0001g0181a0001c0002t0002g0029a0001c0002t0002g0039others(6): Show | 9 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.704+478T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272470 | ||||||
| chr16:31272471
|
T | A | 7 | a0001c0001t0001g0084a0001c0002t0002g0041a0001c0002t0002g0046others(4): Show | 7 | HG02056.hp1 HG02083.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.704+479T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272471 | ||||||
| chr16:31272472
|
T | A | 3 | a0001c0002t0002g0090a0001c0002t0002g0128a0002c0003t0003g0120 | 3 | HG01106.hp2 HG03516.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.704+480T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272472 | ||||||
| chr16:31272473
|
T | A | 3 | a0001c0001t0002g0134a0001c0002t0002g0072a0001c0002t0002g0117 | 3 | HG02809.hp1 NA18994.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.704+481T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272473 | ||||||
| chr16:31272474
|
T | A | 5 | a0001c0001t0001g0064a0001c0001t0002g0136a0001c0002t0002g0082others(2): Show | 5 | HG01106.hp2 NA18522.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+482T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272474 | ||||||
| chr16:31272475
|
T | A | 5 | a0001c0001t0002g0131a0001c0001t0002g0134a0001c0002t0002g0072others(2): Show | 5 | HG02723.hp1 HG02809.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+483T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272475 | ||||||
| chr16:31272476
|
T | A | 3 | a0001c0001t0002g0136a0001c0002t0002g0082a0001c0002t0002g0101 | 3 | NA18522.hp1 NA18747.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.704+484T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272476 | ||||||
| chr16:31272477
|
T | A | 7 | a0001c0001t0001g0177a0001c0001t0001g0237a0001c0001t0002g0134others(4): Show | 7 | HG01516.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.704+485T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272477 | ||||||
| chr16:31272478
|
T | A | 2 | a0001c0001t0001g0173a0001c0001t0002g0136 | 2 | HG01517.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.704+486T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272478 | ||||||
| chr16:31272479
|
T | A | 2 | a0001c0001t0002g0137a0001c0002t0002g0117 | 2 | HG02615.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.704+487T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272479 | ||||||
| chr16:31272535
|
A | G | 19 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(16): Show | 19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.704+543A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272535 | ||||||
| chr16:31272675
|
G | T | 31 | a0001c0007t0009g0142a0002c0003t0003g0016a0002c0003t0003g0060others(28): Show | 31 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.704+683G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272675 | ||||||
| chr16:31272855
|
G | A | 1 | a0004c0006t0003g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.705-510G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31272855 | ||||||
| chr16:31273001
|
C | T | 19 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(16): Show | 19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.705-364C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273001 | ||||||
| chr16:31273096
|
T | C | 19 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(16): Show | 19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.705-269T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273096 | ||||||
| chr16:31273104
|
A | G | 19 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(16): Show | 19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.705-261A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273104 | ||||||
| chr16:31273208
|
A | C | 19 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(16): Show | 19 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.705-157A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273208 | ||||||
| chr16:31273297
|
T | TA | 7 | a0001c0001t0001g0028a0001c0001t0001g0187a0001c0002t0002g0053others(4): Show | 7 | HG00323.hp2 HG02015.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.705-53dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr16 | 31273297 | |||||
| chr16:31273310
|
A | C | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.705-55A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 7/29 | chr16 | 31273310 | ||||||
| chr16:31273611
|
G | A | 2 | a0001c0002t0002g0042a0001c0002t0002g0073 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.858+93G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31273611 | ||||||
| chr16:31273924
|
C | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0223a0008c0015t0001g0172 | 3 | HG03669.hp2 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.858+406C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31273924 | ||||||
| chr16:31274053
|
G | T | 1 | a0001c0002t0002g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.858+535G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274053 | ||||||
| chr16:31274135
|
G | C | 1 | a0001c0005t0004g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.858+617G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274135 | ||||||
| chr16:31274410
|
C | T | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.858+892C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274410 | ||||||
| chr16:31274478
|
C | G | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.858+960C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274478 | ||||||
| chr16:31274572
|
G | T | 13 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(10): Show | 13 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.859-977G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274572 | ||||||
| chr16:31274608
|
T | A | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.859-941T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274608 | ||||||
| chr16:31274610
|
A | ATATTTAT others(1): Show |
21 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.859-925_859-918dup others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | |||||
| chr16:31274610
|
A | ATTTATT | 30 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0007t0004g0109others(27): Show | 30 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.859-938_859-937ins others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | |||||
| chr16:31274610
|
A | ATTTATTT others(3): Show |
11 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(8): Show | 11 | HG02630.hp2 HG02647.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.859-938_859-937ins others(10): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | |||||
| chr16:31274610
|
A | ATTTATTT others(7): Show |
11 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(8): Show | 11 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.859-938_859-937ins others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | |||||
| chr16:31274610
|
A | ATTTATTT others(11): Show |
1 | a0001c0001t0002g0136 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.859-938_859-937ins others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr16 | 31274610 | |||||
| chr16:31274693
|
C | A | 49 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(46): Show | 49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.859-856C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274693 | ||||||
| chr16:31274709
|
G | A | 49 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(46): Show | 49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.859-840G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274709 | ||||||
| chr16:31274965
|
G | T | 6 | a0001c0001t0004g0147a0001c0007t0004g0143a0001c0007t0004g0144others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-584G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31274965 | ||||||
| chr16:31275375
|
C | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0177a0001c0001t0001g0237 | 3 | HG01516.hp2 HG01517.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.859-174C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 8/29 | chr16 | 31275375 | ||||||
| chr16:31275827
|
A | T | 49 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(46): Show | 49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1009+128A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31275827 | ||||||
| chr16:31276106
|
A | T | 99 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(96): Show | 100 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.1009+407A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276106 | ||||||
| chr16:31276148
|
A | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0179a0001c0001t0001g0206others(4): Show | 7 | HG02683.hp2 HG02735.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+449A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276148 | ||||||
| chr16:31276328
|
T | C | 47 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(44): Show | 47 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1010-343T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276328 | ||||||
| chr16:31276476
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1010-195C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276476 | ||||||
| chr16:31276486
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1010-185C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276486 | ||||||
| chr16:31276488
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1010-183C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276488 | ||||||
| chr16:31276582
|
T | G | 13 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(10): Show | 13 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1010-89T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 9/29 | chr16 | 31276582 | ||||||
| chr16:31276800
|
A | C | 54 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(51): Show | 54 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1083+56A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 10/29 | chr16 | 31276800 | ||||||
| chr16:31277240
|
G | A | 21 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(18): Show | 21 | HG01496.hp2 HG02280.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.1213+191G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277240 | ||||||
| chr16:31277287
|
C | T | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1213+238C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277287 | ||||||
| chr16:31277359
|
A | AT | 38 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(35): Show | 38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1213+325dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr16 | 31277359 | |||||
| chr16:31277359
|
A | ATT | 15 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(12): Show | 15 | HG02055.hp2 HG02280.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1213+324_1213+325d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr16 | 31277359 | |||||
| chr16:31277444
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1213+395C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277444 | ||||||
| chr16:31277460
|
G | A | 1 | a0001c0007t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1213+411G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277460 | ||||||
| chr16:31277538
|
A | C | 5 | a0001c0007t0004g0143a0001c0007t0004g0144a0001c0007t0004g0145others(2): Show | 5 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214-429A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277538 | ||||||
| chr16:31277593
|
G | A | 46 | a0001c0001t0001g0208a0001c0007t0004g0023a0001c0007t0004g0024others(43): Show | 46 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1214-374G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277593 | ||||||
| chr16:31277735
|
C | T | 1 | a0001c0002t0002g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1214-232C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277735 | ||||||
| chr16:31277745
|
G | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1214-222G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277745 | ||||||
| chr16:31277788
|
C | T | 21 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1214-179C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277788 | ||||||
| chr16:31277806
|
T | C | 23 | a0003c0004t0005g0019a0003c0004t0005g0022a0003c0004t0005g0025others(20): Show | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1214-161T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277806 | ||||||
| chr16:31277943
|
C | A | 2 | a0001c0002t0002g0180a0001c0002t0002g0229 | 2 | NA18960.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1214-24C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 11/29 | chr16 | 31277943 | ||||||
| chr16:31278197
|
T | C | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+88T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278197 | ||||||
| chr16:31278207
|
G | A | 1 | a0001c0002t0002g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1356+98G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278207 | ||||||
| chr16:31278544
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1356+435G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278544 | ||||||
| chr16:31278623
|
T | C | 1 | a0001c0002t0002g0186 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1356+514T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278623 | ||||||
| chr16:31278882
|
T | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+773T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278882 | ||||||
| chr16:31278972
|
G | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+863G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278972 | ||||||
| chr16:31278982
|
G | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+873G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278982 | ||||||
| chr16:31278983
|
C | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+874C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278983 | ||||||
| chr16:31278984
|
A | G | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+875A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31278984 | ||||||
| chr16:31279038
|
T | G | 1 | a0004c0006t0003g0007 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1356+929T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279038 | ||||||
| chr16:31279129
|
G | A | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+1020G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279129 | ||||||
| chr16:31279141
|
T | C | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356+1032T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279141 | ||||||
| chr16:31279199
|
T | C | 44 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(41): Show | 44 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1356+1090T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279199 | ||||||
| chr16:31279236
|
T | C | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+1127T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279236 | ||||||
| chr16:31279582
|
G | A | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+1473G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279582 | ||||||
| chr16:31279660
|
T | G | 1 | a0001c0002t0002g0044 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1356+1551T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279660 | ||||||
| chr16:31279688
|
G | T | 1 | a0001c0002t0002g0067 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1356+1579G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279688 | ||||||
| chr16:31279739
|
T | G | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1356+1630T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279739 | ||||||
| chr16:31279799
|
A | T | 2 | a0001c0002t0002g0180a0001c0002t0002g0229 | 2 | NA18960.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1356+1690A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31279799 | ||||||
| chr16:31280018
|
T | TG | 69 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0147others(66): Show | 70 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1356+1909_1356+191 others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280018 | ||||||
| chr16:31280169
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0224 | 2 | HG02523.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1356+2060G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280169 | ||||||
| chr16:31280249
|
C | T | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1356+2140C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280249 | ||||||
| chr16:31280257
|
T | C | 1 | a0004c0006t0003g0002 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1356+2148T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280257 | ||||||
| chr16:31280630
|
G | A | 69 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0147others(66): Show | 70 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1356+2521G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280630 | ||||||
| chr16:31280675
|
G | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+2566G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280675 | ||||||
| chr16:31280689
|
A | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+2580A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280689 | ||||||
| chr16:31280889
|
C | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+2780C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280889 | ||||||
| chr16:31280910
|
T | G | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+2801T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31280910 | ||||||
| chr16:31281219
|
C | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+3110C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281219 | ||||||
| chr16:31281271
|
C | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+3162C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281271 | ||||||
| chr16:31281292
|
T | C | 1 | a0001c0002t0002g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1356+3183T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281292 | ||||||
| chr16:31281299
|
A | G | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356+3190A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281299 | ||||||
| chr16:31281309
|
T | C | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356+3200T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281309 | ||||||
| chr16:31281339
|
C | T | 2 | a0005c0009t0002g0050a0005c0009t0002g0093 | 2 | HG02040.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1356+3230C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281339 | ||||||
| chr16:31281452
|
G | T | 23 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0005t0004g0001others(20): Show | 24 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1356+3343G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281452 | ||||||
| chr16:31281635
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1356+3526G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281635 | ||||||
| chr16:31281673
|
C | T | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356+3564C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281673 | ||||||
| chr16:31281823
|
T | G | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1356+3714T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31281823 | ||||||
| chr16:31282236
|
C | T | 2 | a0001c0002t0002g0069a0001c0013t0008g0175 | 2 | HG01192.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1356+4127C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31282236 | ||||||
| chr16:31282362
|
G | T | 1 | a0001c0002t0002g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1356+4253G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31282362 | ||||||
| chr16:31282815
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0210 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1356+4706G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31282815 | ||||||
| chr16:31282879
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+4770G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31282879 | ||||||
| chr16:31283012
|
A | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG01192.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1356+4903A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283012 | ||||||
| chr16:31283150
|
C | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0189a0001c0002t0002g0168others(1): Show | 4 | NA18951.hp1 NA18966.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1356+5041C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283150 | ||||||
| chr16:31283196
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1356+5087C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283196 | ||||||
| chr16:31283213
|
T | C | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1356+5104T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283213 | ||||||
| chr16:31283303
|
C | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+5194C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283303 | ||||||
| chr16:31283364
|
C | T | 1 | a0001c0001t0002g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1356+5255C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283364 | ||||||
| chr16:31283744
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1356+5635C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283744 | ||||||
| chr16:31283837
|
G | T | 2 | a0001c0005t0004g0162a0010c0012t0004g0164 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1356+5728G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283837 | ||||||
| chr16:31283841
|
C | T | 2 | a0001c0005t0004g0162a0010c0012t0004g0164 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1356+5732C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31283841 | ||||||
| chr16:31284223
|
A | G | 239 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1356+6114A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284223 | ||||||
| chr16:31284279
|
C | T | 1 | a0001c0002t0002g0029 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1356+6170C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284279 | ||||||
| chr16:31284416
|
C | G | 1 | a0001c0002t0002g0108 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1356+6307C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284416 | ||||||
| chr16:31284487
|
G | A | 1 | a0003c0004t0005g0025 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1356+6378G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284487 | ||||||
| chr16:31284488
|
C | CA | 94 | a0001c0001t0002g0174a0001c0001t0004g0114a0001c0001t0004g0115others(91): Show | 95 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1356+6379_1356+638 others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284488 | ||||||
| chr16:31284577
|
G | A | 1 | a0001c0002t0002g0056 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1356+6468G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284577 | ||||||
| chr16:31284697
|
G | T | 1 | a0001c0002t0002g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1356+6588G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284697 | ||||||
| chr16:31284798
|
G | A | 1 | a0001c0005t0004g0243 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1356+6689G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284798 | ||||||
| chr16:31284811
|
G | A | 1 | a0002c0003t0003g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1356+6702G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284811 | ||||||
| chr16:31284840
|
G | A | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+6731G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31284840 | ||||||
| chr16:31285014
|
C | T | 2 | a0001c0001t0001g0214a0008c0015t0001g0172 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1356+6905C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285014 | ||||||
| chr16:31285391
|
A | G | 1 | a0003c0004t0005g0019 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1356+7282A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285391 | ||||||
| chr16:31285496
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1356+7387G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285496 | ||||||
| chr16:31285504
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+7395G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285504 | ||||||
| chr16:31285815
|
T | C | 1 | a0004c0006t0003g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1356+7706T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285815 | ||||||
| chr16:31285825
|
G | T | 23 | a0003c0004t0005g0019a0003c0004t0005g0022a0003c0004t0005g0025others(20): Show | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1356+7716G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31285825 | ||||||
| chr16:31286180
|
AT | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1356+8082delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31286180 | |||||
| chr16:31286679
|
C | T | 2 | a0001c0005t0004g0162a0010c0012t0004g0164 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1356+8570C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31286679 | ||||||
| chr16:31286693
|
GTTAT | G | 3 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0139 | 3 | HG02280.hp1 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1356+8587_1356+859 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31286693 | |||||
| chr16:31287148
|
C | T | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1356+9039C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287148 | ||||||
| chr16:31287202
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1356+9093T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287202 | ||||||
| chr16:31287368
|
G | A | 23 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0005t0004g0001others(20): Show | 24 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1356+9259G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287368 | ||||||
| chr16:31287618
|
T | G | 94 | a0001c0001t0002g0174a0001c0001t0004g0114a0001c0001t0004g0115others(91): Show | 95 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1356+9509T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287618 | ||||||
| chr16:31287693
|
G | A | 2 | a0002c0003t0003g0110a0002c0003t0003g0113 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1356+9584G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287693 | ||||||
| chr16:31287833
|
GA | G | 23 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0005t0004g0001others(20): Show | 24 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1357-9675delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31287833 | |||||
| chr16:31287848
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-9666G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287848 | ||||||
| chr16:31287854
|
C | T | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1357-9660C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31287854 | ||||||
| chr16:31288043
|
A | G | 1 | a0003c0004t0005g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1357-9471A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288043 | ||||||
| chr16:31288153
|
A | G | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357-9361A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288153 | ||||||
| chr16:31288159
|
T | C | 1 | a0001c0002t0002g0101 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1357-9355T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288159 | ||||||
| chr16:31288305
|
C | T | 23 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0005t0004g0001others(20): Show | 24 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1357-9209C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288305 | ||||||
| chr16:31288355
|
AAATGTTT others(3): Show |
A | 2 | a0001c0005t0004g0157a0001c0005t0004g0159 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1357-9158_1357-914 others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288355 | ||||||
| chr16:31288454
|
C | T | 31 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(28): Show | 31 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1357-9060C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288454 | ||||||
| chr16:31288783
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1357-8731C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31288783 | ||||||
| chr16:31289045
|
T | C | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357-8469T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289045 | ||||||
| chr16:31289108
|
C | T | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1357-8406C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289108 | ||||||
| chr16:31289268
|
T | G | 1 | a0003c0004t0005g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8246T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289268 | ||||||
| chr16:31289269
|
G | A | 1 | a0003c0004t0005g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8245G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289269 | ||||||
| chr16:31289271
|
C | T | 1 | a0003c0004t0005g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8243C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289271 | ||||||
| chr16:31289299
|
T | C | 1 | a0003c0004t0005g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8215T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289299 | ||||||
| chr16:31289305
|
C | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-8209C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289305 | ||||||
| chr16:31289306
|
G | A | 1 | a0003c0004t0005g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8208G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289306 | ||||||
| chr16:31289307
|
A | T | 1 | a0003c0004t0005g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1357-8207A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289307 | ||||||
| chr16:31289318
|
C | T | 2 | a0002c0003t0003g0112a0003c0004t0005g0054 | 2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1357-8196C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289318 | ||||||
| chr16:31289322
|
T | A | 2 | a0002c0003t0003g0112a0003c0004t0005g0054 | 2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1357-8192T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289322 | ||||||
| chr16:31289448
|
T | C | 94 | a0001c0001t0002g0174a0001c0001t0004g0114a0001c0001t0004g0115others(91): Show | 95 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1357-8066T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289448 | ||||||
| chr16:31289690
|
A | G | 94 | a0001c0001t0002g0174a0001c0001t0004g0114a0001c0001t0004g0115others(91): Show | 95 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1357-7824A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289690 | ||||||
| chr16:31289804
|
G | A | 73 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0064others(70): Show | 73 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1357-7710G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289804 | ||||||
| chr16:31289899
|
T | C | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-7615T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289899 | ||||||
| chr16:31289940
|
G | A | 1 | a0001c0002t0002g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1357-7574G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289940 | ||||||
| chr16:31289996
|
G | A | 2 | a0001c0007t0009g0142a0007c0011t0004g0017 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1357-7518G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31289996 | ||||||
| chr16:31290045
|
C | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-7469C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290045 | ||||||
| chr16:31290080
|
C | CA | 9 | a0001c0001t0001g0032a0001c0001t0001g0103a0001c0001t0001g0226others(6): Show | 9 | HG00741.hp2 HG01192.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357-7413dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31290080 | |||||
| chr16:31290080
|
CA | C | 24 | a0001c0001t0001g0212a0001c0001t0001g0236a0001c0001t0002g0131others(21): Show | 24 | HG01257.hp2 HG01891.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.1357-7413delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31290080 | |||||
| chr16:31290080
|
CAA | C | 19 | a0001c0001t0002g0076a0001c0005t0004g0001a0001c0005t0004g0149others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1357-7414_1357-741 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31290080 | |||||
| chr16:31290099
|
A | G | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357-7415A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290099 | ||||||
| chr16:31290157
|
G | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-7357G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290157 | ||||||
| chr16:31290589
|
G | C | 69 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0147others(66): Show | 70 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1357-6925G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290589 | ||||||
| chr16:31290822
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1357-6692T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31290822 | ||||||
| chr16:31291082
|
GGA | G | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1357-6425_1357-642 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31291082 | |||||
| chr16:31291142
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1357-6372A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291142 | ||||||
| chr16:31291289
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1357-6225C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291289 | ||||||
| chr16:31291513
|
C | T | 21 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357-6001C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291513 | ||||||
| chr16:31291519
|
G | A | 2 | a0002c0003t0003g0110a0002c0003t0003g0113 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1357-5995G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291519 | ||||||
| chr16:31291612
|
G | A | 9 | a0002c0003t0003g0016a0002c0003t0003g0122a0002c0003t0003g0123others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357-5902G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291612 | ||||||
| chr16:31291617
|
A | G | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-5897A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291617 | ||||||
| chr16:31291733
|
A | C | 1 | a0001c0002t0002g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1357-5781A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291733 | ||||||
| chr16:31291880
|
T | C | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357-5634T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31291880 | ||||||
| chr16:31292049
|
C | T | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357-5465C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292049 | ||||||
| chr16:31292139
|
T | C | 1 | a0001c0002t0002g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1357-5375T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292139 | ||||||
| chr16:31292237
|
A | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-5277A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292237 | ||||||
| chr16:31292371
|
A | AT | 21 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357-5143_1357-514 others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292371 | ||||||
| chr16:31292372
|
G | A | 21 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357-5142G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292372 | ||||||
| chr16:31292625
|
C | T | 68 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0005t0004g0001others(65): Show | 69 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.1357-4889C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292625 | ||||||
| chr16:31292629
|
G | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1357-4885G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292629 | ||||||
| chr16:31292679
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1357-4835G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292679 | ||||||
| chr16:31292839
|
T | C | 1 | a0001c0005t0004g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1357-4675T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292839 | ||||||
| chr16:31292968
|
T | G | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1357-4546T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31292968 | ||||||
| chr16:31293061
|
C | T | 28 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(25): Show | 28 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1357-4453C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293061 | ||||||
| chr16:31293137
|
T | C | 1 | a0003c0004t0005g0078 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1357-4377T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293137 | ||||||
| chr16:31293353
|
TCTTC | T | 33 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(30): Show | 34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357-4159_1357-415 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31293353 | |||||
| chr16:31293385
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-4129A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293385 | ||||||
| chr16:31293533
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1357-3981A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293533 | ||||||
| chr16:31293572
|
T | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG01175.hp2 HG01952.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1357-3942T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293572 | ||||||
| chr16:31293969
|
A | G | 78 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(75): Show | 79 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.1357-3545A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31293969 | ||||||
| chr16:31294002
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0210 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1357-3512G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294002 | ||||||
| chr16:31294047
|
G | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1357-3467G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294047 | ||||||
| chr16:31294272
|
A | C | 104 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(101): Show | 105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1357-3242A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294272 | ||||||
| chr16:31294486
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1357-3028T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294486 | ||||||
| chr16:31294570
|
C | T | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1357-2944C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294570 | ||||||
| chr16:31294618
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1357-2896G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294618 | ||||||
| chr16:31294857
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1357-2657G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294857 | ||||||
| chr16:31294999
|
T | C | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1357-2515T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31294999 | ||||||
| chr16:31295143
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357-2371G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31295143 | ||||||
| chr16:31295719
|
T | C | 3 | a0004c0006t0003g0007a0004c0006t0003g0009a0004c0006t0003g0011 | 3 | HG02895.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1357-1795T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31295719 | ||||||
| chr16:31295872
|
T | C | 2 | a0001c0002t0002g0101a0001c0002t0002g0117 | 2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1357-1642T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31295872 | ||||||
| chr16:31295902
|
G | A | 2 | a0001c0007t0009g0142a0007c0011t0004g0017 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1357-1612G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31295902 | ||||||
| chr16:31296063
|
C | T | 7 | a0001c0002t0002g0035a0001c0002t0002g0043a0001c0002t0002g0045others(4): Show | 7 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357-1451C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296063 | ||||||
| chr16:31296106
|
C | CT | 7 | a0001c0001t0001g0100a0001c0001t0001g0178a0001c0001t0001g0216others(4): Show | 7 | HG01255.hp1 HG02135.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357-1390dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31296106 | |||||
| chr16:31296106
|
CT | C | 63 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0002g0131others(60): Show | 64 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.1357-1390delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31296106 | |||||
| chr16:31296271
|
A | AT | 126 | a0001c0001t0001g0020a0001c0001t0001g0075a0001c0001t0001g0081others(123): Show | 126 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1357-1230dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31296271 | |||||
| chr16:31296301
|
T | C | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1357-1213T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296301 | ||||||
| chr16:31296457
|
AC | A | 7 | a0001c0007t0004g0023a0001c0007t0004g0109a0001c0007t0004g0143others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357-1056delC | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296457 | ||||||
| chr16:31296516
|
C | T | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357-998C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296516 | ||||||
| chr16:31296580
|
TATGAGGC others(28): Show |
T | 1 | a0001c0001t0001g0020 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1357-930_1357-896d others(37): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr16 | 31296580 | |||||
| chr16:31296710
|
A | G | 1 | a0002c0003t0003g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1357-804A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296710 | ||||||
| chr16:31296960
|
C | T | 33 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(30): Show | 34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357-554C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31296960 | ||||||
| chr16:31297169
|
A | T | 1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1357-345A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 12/29 | chr16 | 31297169 | ||||||
| chr16:31297670
|
A | C | 1 | a0001c0005t0004g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1497+16A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 13/29 | chr16 | 31297670 | ||||||
| chr16:31297689
|
C | T | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1497+35C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 13/29 | chr16 | 31297689 | ||||||
| chr16:31298204
|
C | CA | 52 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0170others(49): Show | 52 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1707+274dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | |||||
| chr16:31298204
|
C | CAA | 25 | a0001c0001t0004g0147a0001c0005t0004g0001a0001c0005t0004g0149others(22): Show | 26 | HG00733.hp2 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1707+273_1707+274d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | |||||
| chr16:31298204
|
C | CAAA | 25 | a0001c0005t0004g0160a0002c0003t0003g0016a0002c0003t0003g0061others(22): Show | 25 | HG00323.hp1 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1707+272_1707+274d others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | |||||
| chr16:31298204
|
C | CAAAA | 9 | a0002c0003t0003g0060a0002c0003t0003g0102a0002c0003t0003g0111others(6): Show | 9 | HG00741.hp1 HG01516.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707+271_1707+274d others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | |||||
| chr16:31298204
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1707+265_1707+274d others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | |||||
| chr16:31298204
|
CAAAAAAA others(4): Show |
C | 9 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(6): Show | 9 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+264_1707+274d others(13): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298204 | |||||
| chr16:31298281
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+327G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298281 | ||||||
| chr16:31298343
|
A | G | 23 | a0003c0004t0005g0019a0003c0004t0005g0022a0003c0004t0005g0025others(20): Show | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1707+389A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298343 | ||||||
| chr16:31298386
|
C | T | 1 | a0003c0004t0005g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1707+432C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298386 | ||||||
| chr16:31298484
|
C | T | 15 | a0001c0001t0001g0167a0001c0001t0001g0178a0001c0001t0001g0181others(12): Show | 15 | HG00099.hp2 HG00642.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1707+530C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298484 | ||||||
| chr16:31298624
|
G | C | 3 | a0001c0002t0002g0067a0001c0002t0002g0071a0001c0002t0002g0094 | 3 | HG02080.hp1 NA18951.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1707+670G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298624 | ||||||
| chr16:31298795
|
T | G | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+841T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298795 | ||||||
| chr16:31298831
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1707+877G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298831 | ||||||
| chr16:31298833
|
C | CT | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+881dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31298833 | |||||
| chr16:31298935
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0232 | 2 | HG00609.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1707+981G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298935 | ||||||
| chr16:31298984
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+1030A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31298984 | ||||||
| chr16:31299051
|
T | C | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1707+1097T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299051 | ||||||
| chr16:31299192
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1707+1238C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299192 | ||||||
| chr16:31299293
|
A | G | 1 | a0001c0007t0004g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1707+1339A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299293 | ||||||
| chr16:31299321
|
G | C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+1367G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299321 | ||||||
| chr16:31299536
|
C | T | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1707+1582C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299536 | ||||||
| chr16:31299749
|
TCTCCTCC others(20): Show |
T | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1707+1803_1707+182 others(31): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31299749 | |||||
| chr16:31299765
|
T | TTCC | 24 | a0001c0001t0002g0174a0001c0013t0008g0175a0003c0004t0005g0019others(21): Show | 24 | HG01109.hp2 HG01175.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1707+1827_1707+182 others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31299765 | |||||
| chr16:31299775
|
T | TCCC | 77 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(74): Show | 78 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1707+1823_1707+182 others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31299775 | |||||
| chr16:31299836
|
C | A | 1 | a0001c0002t0002g0044 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1707+1882C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299836 | ||||||
| chr16:31299844
|
T | TCTC | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+1911_1707+191 others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31299844 | |||||
| chr16:31299865
|
C | A | 1 | a0001c0002t0002g0108 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1707+1911C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31299865 | ||||||
| chr16:31300018
|
C | A | 33 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(30): Show | 34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+2064C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300018 | ||||||
| chr16:31300053
|
G | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+2099G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300053 | ||||||
| chr16:31300394
|
G | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+2440G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300394 | ||||||
| chr16:31300422
|
T | C | 1 | a0002c0003t0003g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1707+2468T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300422 | ||||||
| chr16:31300508
|
A | T | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+2554A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300508 | ||||||
| chr16:31300676
|
C | T | 1 | a0001c0007t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1707+2722C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300676 | ||||||
| chr16:31300677
|
G | A | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+2723G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300677 | ||||||
| chr16:31300685
|
T | C | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1707+2731T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300685 | ||||||
| chr16:31300732
|
A | G | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1707+2778A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300732 | ||||||
| chr16:31300740
|
A | G | 3 | a0003c0004t0005g0022a0003c0004t0005g0086a0003c0004t0005g0095 | 3 | HG02257.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1707+2786A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300740 | ||||||
| chr16:31300791
|
A | G | 1 | a0001c0002t0002g0072 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1707+2837A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300791 | ||||||
| chr16:31300836
|
C | T | 21 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1707+2882C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300836 | ||||||
| chr16:31300861
|
G | A | 2 | a0001c0005t0004g0158a0001c0005t0004g0161 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1707+2907G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300861 | ||||||
| chr16:31300911
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+2957C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300911 | ||||||
| chr16:31300965
|
A | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0202others(4): Show | 7 | HG00673.hp2 HG01192.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+3011A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31300965 | ||||||
| chr16:31301180
|
T | G | 25 | a0001c0001t0002g0174a0001c0013t0008g0175a0003c0004t0005g0019others(22): Show | 25 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1707+3226T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31301180 | ||||||
| chr16:31301534
|
T | C | 11 | a0001c0002t0002g0035a0001c0002t0002g0043a0001c0002t0002g0045others(8): Show | 11 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+3580T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31301534 | ||||||
| chr16:31301564
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+3610T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31301564 | ||||||
| chr16:31301932
|
C | T | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1707+3978C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31301932 | ||||||
| chr16:31302039
|
A | C | 2 | a0001c0002t0002g0029a0002c0003t0003g0102 | 2 | HG00673.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1707+4085A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302039 | ||||||
| chr16:31302376
|
T | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+4422T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302376 | ||||||
| chr16:31302378
|
CTTTTCTT others(5): Show |
C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+4439_1707+445 others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302378 | |||||
| chr16:31302396
|
T | TTTCTTTC | 6 | a0003c0004t0005g0019a0003c0004t0005g0047a0003c0004t0005g0097others(3): Show | 6 | HG01256.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | |||||
| chr16:31302396
|
T | TTTCTTTC others(4): Show |
7 | a0003c0004t0005g0025a0003c0004t0005g0031a0003c0004t0005g0054others(4): Show | 7 | HG01109.hp2 HG01255.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | |||||
| chr16:31302396
|
T | TTTCTTTC others(8): Show |
1 | a0003c0004t0005g0077 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1707+4444_1707+444 others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | |||||
| chr16:31302396
|
T | TTTCTTTC others(23): Show |
3 | a0003c0004t0005g0036a0003c0004t0005g0051a0003c0004t0005g0079 | 3 | HG00099.hp1 HG03098.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(34): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | |||||
| chr16:31302396
|
T | TTTCTTTC others(27): Show |
1 | a0003c0004t0005g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1707+4444_1707+444 others(38): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | |||||
| chr16:31302396
|
T | TTTCTTTC others(39): Show |
2 | a0003c0004t0005g0027a0003c0004t0005g0095 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(50): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | |||||
| chr16:31302396
|
T | TTTCTTTC others(43): Show |
2 | a0003c0004t0005g0022a0003c0004t0005g0096 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1707+4444_1707+444 others(54): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | |||||
| chr16:31302396
|
T | TTTCTTTC others(43): Show |
1 | a0003c0004t0005g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1707+4444_1707+444 others(54): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302396 | |||||
| chr16:31302398
|
TTCTTTTC others(53): Show |
T | 2 | a0001c0005t0004g0162a0010c0012t0004g0164 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1707+4445_1707+450 others(64): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302398 | ||||||
| chr16:31302401
|
T | TTTC | 13 | a0003c0004t0005g0019a0003c0004t0005g0025a0003c0004t0005g0031others(10): Show | 13 | HG01109.hp2 HG01255.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1707+4449_1707+445 others(7): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302401 | |||||
| chr16:31302404
|
T | C | 9 | a0003c0004t0005g0022a0003c0004t0005g0027a0003c0004t0005g0036others(6): Show | 9 | HG00099.hp1 HG01175.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707+4450T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302404 | ||||||
| chr16:31302405
|
C | T | 9 | a0003c0004t0005g0022a0003c0004t0005g0027a0003c0004t0005g0036others(6): Show | 9 | HG00099.hp1 HG01175.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707+4451C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302405 | ||||||
| chr16:31302408
|
T | C | 18 | a0001c0002t0002g0090a0003c0004t0005g0022a0003c0004t0005g0025others(15): Show | 18 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1707+4454T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302408 | ||||||
| chr16:31302408
|
TTTTC | T | 14 | a0001c0007t0004g0024a0001c0007t0004g0148a0002c0003t0003g0060others(11): Show | 14 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1707+4473_1707+447 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302408 | |||||
| chr16:31302409
|
T | C | 6 | a0003c0004t0005g0019a0003c0004t0005g0047a0003c0004t0005g0097others(3): Show | 6 | HG01256.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+4455T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302409 | ||||||
| chr16:31302417
|
TTTCTTTC others(4): Show |
T | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1707+4477_1707+448 others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302417 | |||||
| chr16:31302424
|
CTTTCTTC others(1): Show |
C | 15 | a0001c0007t0004g0109a0001c0007t0004g0143a0001c0007t0004g0145others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1707+4473_1707+448 others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302424 | |||||
| chr16:31302424
|
CTTTCTTC others(5): Show |
C | 3 | a0001c0007t0004g0023a0001c0007t0004g0144a0001c0007t0004g0146 | 3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1707+4473_1707+448 others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302424 | |||||
| chr16:31302424
|
CTTTCTTC others(17): Show |
C | 1 | a0002c0003t0003g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1707+4473_1707+449 others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302424 | |||||
| chr16:31302424
|
CTTTCTTC others(55): Show |
C | 12 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(9): Show | 13 | HG02258.hp2 HG02622.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1707+4477_1707+453 others(66): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302424 | |||||
| chr16:31302426
|
TTCTTCTT others(21): Show |
T | 1 | a0002c0003t0003g0111 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1707+4473_1707+450 others(32): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302426 | ||||||
| chr16:31302426
|
TTCTTCTT others(25): Show |
T | 1 | a0004c0006t0003g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1707+4473_1707+450 others(36): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302426 | ||||||
| chr16:31302427
|
T | C | 7 | a0002c0003t0003g0088a0002c0003t0003g0123a0004c0006t0003g0002others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+4473T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302427 | ||||||
| chr16:31302428
|
C | CT | 17 | a0003c0004t0005g0019a0003c0004t0005g0025a0003c0004t0005g0027others(14): Show | 17 | HG00099.hp1 HG01175.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1707+4476dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302428 | |||||
| chr16:31302428
|
C | CTTCT | 11 | a0001c0001t0001g0028a0001c0001t0001g0195a0001c0001t0001g0208others(8): Show | 11 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1707+4496_1707+449 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302428 | |||||
| chr16:31302428
|
C | CTTTCTTT others(25): Show |
1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4476_1707+447 others(36): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302428 | |||||
| chr16:31302428
|
C | CTTTCTTT others(33): Show |
1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1707+4476_1707+447 others(44): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302428 | |||||
| chr16:31302428
|
C | T | 7 | a0002c0003t0003g0088a0002c0003t0003g0123a0004c0006t0003g0002others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+4474C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302428 | ||||||
| chr16:31302434
|
T | C | 3 | a0003c0004t0005g0022a0003c0004t0005g0051a0003c0004t0005g0095 | 3 | HG02486.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1707+4480T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302434 | ||||||
| chr16:31302438
|
T | C | 1 | a0003c0004t0005g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1707+4484T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302438 | ||||||
| chr16:31302442
|
T | C | 1 | a0003c0004t0005g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1707+4488T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302442 | ||||||
| chr16:31302443
|
CTTTCTTT others(36): Show |
C | 19 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(16): Show | 19 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1707+4498_1707+454 others(47): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302443 | |||||
| chr16:31302446
|
T | C | 4 | a0003c0004t0005g0027a0003c0004t0005g0031a0003c0004t0005g0036others(1): Show | 4 | HG01175.hp1 HG02735.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+4492T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302446 | ||||||
| chr16:31302450
|
TCTTCCTT others(1): Show |
T | 16 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0144others(13): Show | 16 | HG01256.hp1 HG01258.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1707+4500_1707+450 others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302450 | |||||
| chr16:31302454
|
C | CCTTT | 4 | a0003c0004t0005g0019a0003c0004t0005g0025a0003c0004t0005g0047others(1): Show | 4 | HG01109.hp2 HG01256.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+4503_1707+450 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302454 | |||||
| chr16:31302454
|
C | T | 165 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.1707+4500C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302454 | ||||||
| chr16:31302458
|
C | T | 53 | a0001c0001t0004g0147a0001c0007t0004g0109a0001c0007t0004g0143others(50): Show | 53 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1707+4504C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302458 | ||||||
| chr16:31302458
|
CCTTT | C | 7 | a0001c0001t0001g0100a0001c0001t0001g0173a0001c0001t0001g0177others(4): Show | 7 | HG01358.hp2 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+4529_1707+453 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302458 | |||||
| chr16:31302462
|
T | C | 126 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(123): Show | 126 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1707+4508T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302462 | ||||||
| chr16:31302466
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1707+4512T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302466 | ||||||
| chr16:31302466
|
T | TCTTC | 8 | a0003c0004t0005g0054a0003c0004t0005g0077a0003c0004t0005g0097others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+4515_1707+451 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302466 | |||||
| chr16:31302483
|
CT | C | 43 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(40): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1707+4535delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302483 | |||||
| chr16:31302487
|
T | C | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4533T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302487 | ||||||
| chr16:31302490
|
C | T | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4536C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302490 | ||||||
| chr16:31302495
|
C | T | 2 | a0001c0001t0004g0147a0001c0013t0008g0175 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1707+4541C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302495 | ||||||
| chr16:31302499
|
T | C | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4545T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302499 | ||||||
| chr16:31302503
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+4549T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302503 | ||||||
| chr16:31302691
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1707+4737C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302691 | ||||||
| chr16:31302707
|
TTC | T | 4 | a0003c0004t0005g0036a0003c0004t0005g0037a0003c0004t0005g0078others(1): Show | 4 | HG00099.hp1 HG01175.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+4757_1707+475 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302707 | |||||
| chr16:31302714
|
T | C | 1 | a0001c0002t0002g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1707+4760T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302714 | ||||||
| chr16:31302749
|
C | G | 1 | a0001c0002t0002g0101 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1707+4795C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302749 | ||||||
| chr16:31302872
|
C | T | 3 | a0001c0002t0002g0063a0001c0002t0002g0065a0001c0002t0002g0066 | 3 | HG01257.hp1 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1707+4918C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302872 | ||||||
| chr16:31302884
|
CTCTTTCT others(39): Show |
C | 1 | a0008c0015t0001g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1707+4946_1707+499 others(50): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302884 | |||||
| chr16:31302918
|
C | CTCTT | 11 | a0001c0001t0001g0100a0001c0001t0001g0166a0001c0001t0001g0219others(8): Show | 11 | HG01891.hp1 HG02129.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+5042_1707+504 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
C | CTCTTTCT others(1): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0002t0002g0108others(1): Show | 4 | HG01192.hp1 HG02647.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+5038_1707+504 others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
C | CTCTTTCT others(5): Show |
3 | a0001c0001t0001g0202a0001c0001t0001g0204a0004c0006t0003g0007 | 3 | HG00558.hp2 HG00673.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1707+5034_1707+504 others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
C | CTCTTTCT others(29): Show |
1 | a0001c0002t0002g0045 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1707+5010_1707+504 others(40): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
C | T | 1 | a0001c0007t0004g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1707+4964C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302918 | ||||||
| chr16:31302918
|
CTCTT | C | 42 | a0001c0001t0001g0084a0001c0001t0001g0171a0001c0001t0001g0182others(39): Show | 42 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1707+5042_1707+504 others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(1): Show |
C | 33 | a0001c0001t0001g0118a0001c0001t0001g0170a0001c0001t0001g0195others(30): Show | 33 | HG00609.hp2 HG00642.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1707+5038_1707+504 others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(5): Show |
C | 24 | a0001c0001t0001g0028a0001c0001t0001g0081a0001c0001t0001g0177others(21): Show | 24 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1707+5034_1707+504 others(16): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(9): Show |
C | 35 | a0001c0001t0001g0103a0001c0001t0001g0169a0001c0001t0001g0181others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1707+5030_1707+504 others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(13): Show |
C | 20 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0216others(17): Show | 21 | HG00099.hp1 HG00733.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1707+5026_1707+504 others(24): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(17): Show |
C | 7 | a0001c0001t0001g0167a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG00323.hp2 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+5022_1707+504 others(28): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(21): Show |
C | 9 | a0001c0001t0001g0208a0001c0001t0002g0135a0001c0001t0002g0139others(6): Show | 9 | HG00642.hp1 HG00673.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707+5018_1707+504 others(32): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(25): Show |
C | 7 | a0001c0001t0001g0075a0001c0001t0001g0178a0001c0001t0001g0220others(4): Show | 7 | HG01123.hp2 HG01255.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+5014_1707+504 others(36): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(29): Show |
C | 2 | a0001c0002t0002g0042a0001c0002t0002g0087 | 2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1707+5010_1707+504 others(40): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(33): Show |
C | 1 | a0001c0002t0002g0073 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1707+5006_1707+504 others(44): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302918
|
CTCTTTCT others(53): Show |
C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+4986_1707+504 others(64): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302918 | |||||
| chr16:31302925
|
T | TTTCTTTC others(3): Show |
1 | a0001c0002t0002g0215 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1707+4980_1707+498 others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302925 | |||||
| chr16:31302926
|
T | TTCTTTCT others(19): Show |
1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+4979_1707+498 others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302926 | |||||
| chr16:31302933
|
T | TCTCTCTC others(11): Show |
1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1707+4979_1707+498 others(22): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302933 | ||||||
| chr16:31302934
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1707+4980T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302934 | ||||||
| chr16:31302972
|
CTTTCTTT others(19): Show |
C | 1 | a0003c0004t0005g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+5028_1707+505 others(30): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302972 | |||||
| chr16:31302984
|
CTTTCTTT others(6): Show |
C | 1 | a0004c0006t0003g0002 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1707+5034_1707+504 others(17): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302984 | |||||
| chr16:31302984
|
CTTTCTTT others(7): Show |
C | 1 | a0001c0002t0002g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1707+5040_1707+505 others(18): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302984 | |||||
| chr16:31302984
|
CTTTCTTT others(8): Show |
C | 1 | a0003c0004t0005g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1707+5033_1707+504 others(19): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302984 | |||||
| chr16:31302988
|
CTTTCTTT others(4): Show |
C | 1 | a0003c0004t0005g0019 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1707+5037_1707+504 others(15): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302988 | |||||
| chr16:31302998
|
T | C | 1 | a0002c0003t0003g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1707+5044T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31302998 | ||||||
| chr16:31302998
|
TTTTCTTT others(9): Show |
T | 1 | a0001c0001t0001g0064 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1707+5050_1707+506 others(20): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31302998 | |||||
| chr16:31303016
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1707+5062T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303016 | ||||||
| chr16:31303016
|
TTC | T | 33 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(30): Show | 34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+5068_1707+506 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31303016 | |||||
| chr16:31303180
|
G | A | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+5226G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303180 | ||||||
| chr16:31303216
|
A | G | 1 | a0001c0002t0002g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1707+5262A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303216 | ||||||
| chr16:31303278
|
T | C | 104 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(101): Show | 105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+5324T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303278 | ||||||
| chr16:31303775
|
G | C | 1 | a0004c0006t0003g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1707+5821G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303775 | ||||||
| chr16:31303800
|
T | C | 2 | a0001c0002t0002g0101a0001c0002t0002g0117 | 2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1707+5846T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31303800 | ||||||
| chr16:31304089
|
A | T | 1 | a0002c0003t0003g0121 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+6135A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304089 | ||||||
| chr16:31304173
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1707+6219G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304173 | ||||||
| chr16:31304260
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+6306C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304260 | ||||||
| chr16:31304363
|
T | C | 1 | a0001c0002t0002g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1707+6409T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304363 | ||||||
| chr16:31304693
|
C | T | 2 | a0001c0007t0009g0142a0007c0011t0004g0017 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1707+6739C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304693 | ||||||
| chr16:31304714
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1707+6760G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31304714 | ||||||
| chr16:31305313
|
C | A | 1 | a0001c0002t0002g0197 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1707+7359C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305313 | ||||||
| chr16:31305489
|
C | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+7535C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305489 | ||||||
| chr16:31305574
|
T | C | 1 | a0001c0002t0002g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1707+7620T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305574 | ||||||
| chr16:31305679
|
C | T | 1 | a0001c0007t0004g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1707+7725C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305679 | ||||||
| chr16:31305704
|
G | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+7750G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305704 | ||||||
| chr16:31305751
|
G | A | 34 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(31): Show | 35 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1707+7797G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305751 | ||||||
| chr16:31305797
|
G | A | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1707+7843G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305797 | ||||||
| chr16:31305917
|
T | C | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+7963T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305917 | ||||||
| chr16:31305941
|
C | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+7987C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31305941 | ||||||
| chr16:31306106
|
T | C | 104 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(101): Show | 105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+8152T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306106 | ||||||
| chr16:31306184
|
G | A | 104 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(101): Show | 105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+8230G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306184 | ||||||
| chr16:31306376
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1707+8422A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306376 | ||||||
| chr16:31306508
|
CT | C | 17 | a0001c0001t0001g0100a0001c0001t0001g0171a0001c0007t0009g0142others(14): Show | 17 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1707+8569delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31306508 | |||||
| chr16:31306569
|
A | G | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+8615A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306569 | ||||||
| chr16:31306631
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1707+8677C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306631 | ||||||
| chr16:31306656
|
A | C | 104 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(101): Show | 105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+8702A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306656 | ||||||
| chr16:31306660
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1707+8706C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306660 | ||||||
| chr16:31306703
|
G | A | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1707+8749G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306703 | ||||||
| chr16:31306757
|
G | A | 1 | a0001c0002t0002g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1707+8803G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306757 | ||||||
| chr16:31306936
|
A | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+8982A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306936 | ||||||
| chr16:31306969
|
CAT | C | 6 | a0001c0002t0002g0035a0001c0002t0002g0043a0001c0002t0002g0055others(3): Show | 6 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+9017_1707+901 others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31306969 | |||||
| chr16:31306976
|
G | C | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+9022G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306976 | ||||||
| chr16:31306993
|
T | C | 104 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(101): Show | 105 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1707+9039T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31306993 | ||||||
| chr16:31307027
|
C | T | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+9073C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307027 | ||||||
| chr16:31307078
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1707+9124C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307078 | ||||||
| chr16:31307127
|
C | T | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+9173C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307127 | ||||||
| chr16:31307128
|
G | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0001g0217others(1): Show | 4 | HG00673.hp2 HG02132.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707+9174G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307128 | ||||||
| chr16:31307502
|
C | G | 3 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0147 | 3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+9548C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307502 | ||||||
| chr16:31307555
|
G | A | 1 | a0001c0002t0002g0021 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1707+9601G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307555 | ||||||
| chr16:31307712
|
C | T | 33 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(30): Show | 34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1707+9758C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307712 | ||||||
| chr16:31307790
|
T | C | 7 | a0001c0007t0004g0023a0001c0007t0004g0109a0001c0007t0004g0143others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1707+9836T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307790 | ||||||
| chr16:31307917
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1707+9963C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307917 | ||||||
| chr16:31307962
|
G | A | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+10008G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31307962 | ||||||
| chr16:31308042
|
C | T | 1 | a0007c0011t0004g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1707+10088C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308042 | ||||||
| chr16:31308044
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1707+10090G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308044 | ||||||
| chr16:31308076
|
A | C | 81 | a0001c0001t0001g0177a0001c0001t0001g0216a0001c0001t0002g0076others(78): Show | 82 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1707+10122A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308076 | ||||||
| chr16:31308115
|
T | C | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707+10161T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308115 | ||||||
| chr16:31308181
|
T | G | 3 | a0002c0003t0003g0119a0002c0003t0003g0120a0002c0003t0003g0121 | 3 | HG00741.hp2 HG01106.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1707+10227T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308181 | ||||||
| chr16:31308200
|
T | C | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+10246T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308200 | ||||||
| chr16:31308300
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+10346G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308300 | ||||||
| chr16:31308420
|
T | G | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1707+10466T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308420 | ||||||
| chr16:31308435
|
G | A | 7 | a0003c0004t0005g0019a0003c0004t0005g0031a0003c0004t0005g0036others(4): Show | 7 | HG00099.hp1 HG01175.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1707+10481G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308435 | ||||||
| chr16:31308447
|
G | A | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1707+10493G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308447 | ||||||
| chr16:31308454
|
C | T | 1 | a0001c0007t0004g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1707+10500C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308454 | ||||||
| chr16:31308459
|
G | C | 2 | a0002c0003t0003g0110a0002c0003t0003g0113 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1707+10505G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308459 | ||||||
| chr16:31308591
|
C | CA | 21 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1707+10644dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31308591 | |||||
| chr16:31308687
|
C | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+10733C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308687 | ||||||
| chr16:31308711
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+10757T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308711 | ||||||
| chr16:31308737
|
C | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+10783C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308737 | ||||||
| chr16:31308738
|
G | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0210 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1707+10784G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308738 | ||||||
| chr16:31308920
|
C | A | 2 | a0004c0006t0003g0005a0004c0006t0003g0006 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1707+10966C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308920 | ||||||
| chr16:31308977
|
C | A | 81 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.1707+11023C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308977 | ||||||
| chr16:31308979
|
C | A | 1 | a0003c0004t0005g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+11025C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31308979 | ||||||
| chr16:31309083
|
G | A | 1 | a0001c0002t0002g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1707+11129G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309083 | ||||||
| chr16:31309100
|
G | T | 1 | a0003c0004t0005g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+11146G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309100 | ||||||
| chr16:31309101
|
T | G | 1 | a0003c0004t0005g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+11147T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309101 | ||||||
| chr16:31309102
|
G | T | 1 | a0003c0004t0005g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1707+11148G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309102 | ||||||
| chr16:31309169
|
C | T | 3 | a0001c0007t0009g0142a0006c0010t0004g0018a0007c0011t0004g0017 | 3 | HG02896.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1707+11215C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309169 | ||||||
| chr16:31309455
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707+11501C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309455 | ||||||
| chr16:31309554
|
T | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0177a0001c0001t0001g0237 | 3 | HG01516.hp2 HG01517.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1707+11600T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309554 | ||||||
| chr16:31309580
|
C | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1707+11626C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309580 | ||||||
| chr16:31309605
|
C | G | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1708-11636C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309605 | ||||||
| chr16:31309616
|
T | G | 1 | a0001c0002t0002g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1708-11625T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309616 | ||||||
| chr16:31309668
|
T | G | 5 | a0001c0007t0004g0143a0001c0007t0004g0144a0001c0007t0004g0145others(2): Show | 5 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-11573T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309668 | ||||||
| chr16:31309784
|
C | G | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1708-11457C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309784 | ||||||
| chr16:31309793
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-11448G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309793 | ||||||
| chr16:31309794
|
C | T | 1 | a0001c0002t0002g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1708-11447C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309794 | ||||||
| chr16:31309874
|
T | C | 1 | a0001c0007t0004g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1708-11367T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309874 | ||||||
| chr16:31309935
|
A | G | 2 | a0005c0009t0002g0050a0005c0009t0002g0093 | 2 | HG02040.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1708-11306A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31309935 | ||||||
| chr16:31310100
|
C | G | 3 | a0002c0003t0003g0110a0002c0003t0003g0111a0002c0003t0003g0113 | 3 | HG02630.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1708-11141C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310100 | ||||||
| chr16:31310156
|
T | C | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-11085T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310156 | ||||||
| chr16:31310567
|
C | T | 1 | a0001c0007t0004g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1708-10674C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310567 | ||||||
| chr16:31310711
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1708-10530C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310711 | ||||||
| chr16:31310712
|
G | A | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-10529G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310712 | ||||||
| chr16:31310727
|
G | A | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-10514G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310727 | ||||||
| chr16:31310788
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-10453C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310788 | ||||||
| chr16:31310897
|
A | G | 23 | a0003c0004t0005g0019a0003c0004t0005g0022a0003c0004t0005g0025others(20): Show | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-10344A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310897 | ||||||
| chr16:31310926
|
G | C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-10315G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31310926 | ||||||
| chr16:31311013
|
G | A | 25 | a0001c0001t0002g0174a0001c0013t0008g0175a0003c0004t0005g0019others(22): Show | 25 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1708-10228G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311013 | ||||||
| chr16:31311183
|
A | G | 1 | a0004c0006t0003g0002 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1708-10058A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311183 | ||||||
| chr16:31311204
|
C | T | 2 | a0001c0007t0009g0142a0007c0011t0004g0017 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1708-10037C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311204 | ||||||
| chr16:31311212
|
A | G | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1708-10029A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311212 | ||||||
| chr16:31311225
|
C | T | 1 | a0002c0003t0003g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1708-10016C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311225 | ||||||
| chr16:31311531
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-9710A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311531 | ||||||
| chr16:31311892
|
T | C | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1708-9349T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311892 | ||||||
| chr16:31311895
|
A | T | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1708-9346A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311895 | ||||||
| chr16:31311899
|
T | C | 1 | a0001c0013t0008g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1708-9342T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311899 | ||||||
| chr16:31311948
|
C | T | 1 | a0003c0004t0005g0106 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1708-9293C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31311948 | ||||||
| chr16:31312029
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1708-9212G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312029 | ||||||
| chr16:31312251
|
G | A | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-8990G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312251 | ||||||
| chr16:31312260
|
G | T | 1 | a0001c0007t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1708-8981G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312260 | ||||||
| chr16:31312325
|
A | G | 1 | a0001c0002t0002g0104 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1708-8916A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312325 | ||||||
| chr16:31312332
|
C | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-8909C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312332 | ||||||
| chr16:31312355
|
A | G | 23 | a0003c0004t0005g0019a0003c0004t0005g0022a0003c0004t0005g0025others(20): Show | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-8886A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312355 | ||||||
| chr16:31312391
|
A | T | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1708-8850A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312391 | ||||||
| chr16:31312434
|
T | C | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1708-8807T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312434 | ||||||
| chr16:31312463
|
G | A | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1708-8778G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312463 | ||||||
| chr16:31312464
|
T | C | 1 | a0001c0007t0004g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1708-8777T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312464 | ||||||
| chr16:31312595
|
A | T | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-8646A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312595 | ||||||
| chr16:31312629
|
A | G | 2 | a0002c0003t0003g0110a0002c0003t0003g0113 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1708-8612A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312629 | ||||||
| chr16:31312873
|
C | CT | 16 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(13): Show | 16 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.1708-8351dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31312873 | |||||
| chr16:31312873
|
CT | C | 153 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1708-8351delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31312873 | |||||
| chr16:31312974
|
C | T | 7 | a0001c0007t0004g0023a0001c0007t0004g0109a0001c0007t0004g0143others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1708-8267C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312974 | ||||||
| chr16:31312995
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-8246G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31312995 | ||||||
| chr16:31313650
|
C | G | 33 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(30): Show | 34 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-7591C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31313650 | ||||||
| chr16:31313665
|
T | C | 42 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(39): Show | 42 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1708-7576T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31313665 | ||||||
| chr16:31313962
|
C | G | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-7279C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31313962 | ||||||
| chr16:31314112
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1708-7129G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314112 | ||||||
| chr16:31314163
|
C | A | 2 | a0001c0005t0004g0162a0010c0012t0004g0164 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1708-7078C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314163 | ||||||
| chr16:31314268
|
A | C | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1708-6973A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314268 | ||||||
| chr16:31314743
|
T | A | 1 | a0001c0007t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1708-6498T>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314743 | ||||||
| chr16:31314760
|
G | A | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-6481G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314760 | ||||||
| chr16:31314821
|
G | GT | 42 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0193others(39): Show | 42 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1708-6401dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31314821 | |||||
| chr16:31314821
|
GT | G | 29 | a0001c0001t0001g0028a0001c0002t0002g0069a0001c0005t0004g0001others(26): Show | 30 | HG01192.hp2 HG01496.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1708-6401delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31314821 | |||||
| chr16:31314844
|
A | G | 5 | a0003c0004t0005g0022a0003c0004t0005g0051a0003c0004t0005g0086others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-6397A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314844 | ||||||
| chr16:31314883
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1708-6358C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31314883 | ||||||
| chr16:31315035
|
A | T | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1708-6206A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315035 | ||||||
| chr16:31315102
|
C | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-6139C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315102 | ||||||
| chr16:31315103
|
G | A | 1 | a0002c0003t0003g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1708-6138G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315103 | ||||||
| chr16:31315108
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-6133C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315108 | ||||||
| chr16:31315266
|
T | G | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-5975T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315266 | ||||||
| chr16:31315308
|
T | C | 3 | a0001c0002t0002g0063a0001c0002t0002g0065a0001c0002t0002g0066 | 3 | HG01257.hp1 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1708-5933T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315308 | ||||||
| chr16:31315385
|
C | T | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-5856C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315385 | ||||||
| chr16:31315446
|
A | AT | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-5788dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31315446 | |||||
| chr16:31315605
|
C | T | 1 | a0004c0006t0003g0004 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1708-5636C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315605 | ||||||
| chr16:31315607
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-5634G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315607 | ||||||
| chr16:31315724
|
G | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG01175.hp2 HG01952.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1708-5517G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315724 | ||||||
| chr16:31315727
|
G | A | 21 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1708-5514G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315727 | ||||||
| chr16:31315754
|
C | T | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1708-5487C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315754 | ||||||
| chr16:31315858
|
T | C | 23 | a0003c0004t0005g0019a0003c0004t0005g0022a0003c0004t0005g0025others(20): Show | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-5383T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315858 | ||||||
| chr16:31315920
|
C | T | 1 | a0001c0007t0004g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1708-5321C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315920 | ||||||
| chr16:31315922
|
C | T | 1 | a0001c0002t0002g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1708-5319C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315922 | ||||||
| chr16:31315959
|
C | T | 3 | a0001c0007t0009g0142a0006c0010t0004g0018a0007c0011t0004g0017 | 3 | HG02896.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1708-5282C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31315959 | ||||||
| chr16:31316010
|
A | T | 232 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1708-5231A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316010 | ||||||
| chr16:31316016
|
A | G | 232 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1708-5225A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316016 | ||||||
| chr16:31316021
|
C | T | 3 | a0003c0004t0005g0022a0003c0004t0005g0086a0003c0004t0005g0095 | 3 | HG02257.hp2 HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1708-5220C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316021 | ||||||
| chr16:31316038
|
CAAAAAAT others(185): Show |
C | 232 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1708-5196_1708-500 others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31316038 | |||||
| chr16:31316278
|
C | T | 19 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(16): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1708-4963C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316278 | ||||||
| chr16:31316339
|
A | G | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1708-4902A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316339 | ||||||
| chr16:31316387
|
G | GA | 68 | a0001c0001t0001g0020a0001c0001t0001g0194a0001c0001t0001g0239others(65): Show | 68 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1708-4840dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31316387 | |||||
| chr16:31316434
|
G | T | 1 | a0001c0007t0004g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1708-4807G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316434 | ||||||
| chr16:31316691
|
C | T | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-4550C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316691 | ||||||
| chr16:31316939
|
T | C | 5 | a0001c0007t0004g0143a0001c0007t0004g0144a0001c0007t0004g0145others(2): Show | 5 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-4302T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316939 | ||||||
| chr16:31316951
|
T | C | 242 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.1708-4290T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316951 | ||||||
| chr16:31316992
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1708-4249G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31316992 | ||||||
| chr16:31317163
|
C | T | 7 | a0003c0004t0005g0054a0003c0004t0005g0077a0003c0004t0005g0097others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1708-4078C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317163 | ||||||
| chr16:31317341
|
C | T | 1 | a0002c0003t0003g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1708-3900C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317341 | ||||||
| chr16:31317379
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1708-3862G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317379 | ||||||
| chr16:31317559
|
T | G | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-3682T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317559 | ||||||
| chr16:31317670
|
A | T | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-3571A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317670 | ||||||
| chr16:31317949
|
C | G | 2 | a0001c0007t0009g0142a0007c0011t0004g0017 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1708-3292C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317949 | ||||||
| chr16:31317959
|
G | A | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-3282G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31317959 | ||||||
| chr16:31318344
|
C | CT | 18 | a0001c0001t0001g0167a0001c0001t0001g0178a0001c0001t0001g0181others(15): Show | 18 | HG00099.hp2 HG00642.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1708-2880dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31318344 | |||||
| chr16:31318344
|
CT | C | 23 | a0001c0002t0002g0191a0003c0004t0005g0019a0003c0004t0005g0022others(20): Show | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-2880delT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31318344 | |||||
| chr16:31318464
|
C | T | 8 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(5): Show | 8 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1708-2777C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318464 | ||||||
| chr16:31318490
|
C | T | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1708-2751C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318490 | ||||||
| chr16:31318633
|
T | C | 78 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(75): Show | 79 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.1708-2608T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318633 | ||||||
| chr16:31318806
|
A | G | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-2435A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318806 | ||||||
| chr16:31318811
|
TTGTAATT others(3): Show |
T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-2429_1708-242 others(14): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318811 | ||||||
| chr16:31318840
|
A | G | 87 | a0001c0001t0002g0174a0001c0002t0002g0021a0001c0002t0002g0026others(84): Show | 87 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1708-2401A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318840 | ||||||
| chr16:31318857
|
C | T | 23 | a0003c0004t0005g0019a0003c0004t0005g0022a0003c0004t0005g0025others(20): Show | 23 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1708-2384C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318857 | ||||||
| chr16:31318949
|
A | C | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-2292A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31318949 | ||||||
| chr16:31319003
|
TG | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-2237delG | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319003 | ||||||
| chr16:31319214
|
G | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-2027G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319214 | ||||||
| chr16:31319239
|
G | GT | 50 | a0001c0005t0004g0156a0001c0005t0004g0160a0001c0005t0004g0163others(47): Show | 50 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1708-1992dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31319239 | |||||
| chr16:31319405
|
A | G | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-1836A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319405 | ||||||
| chr16:31319686
|
G | C | 62 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(59): Show | 62 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1708-1555G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319686 | ||||||
| chr16:31319816
|
T | C | 45 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1708-1425T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319816 | ||||||
| chr16:31319818
|
C | CT | 22 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(19): Show | 23 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1708-1411dupT | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr16 | 31319818 | |||||
| chr16:31319836
|
G | A | 14 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(11): Show | 15 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1708-1405G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319836 | ||||||
| chr16:31319839
|
A | G | 166 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(163): Show | 167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1708-1402A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319839 | ||||||
| chr16:31319881
|
C | T | 34 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(31): Show | 34 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1708-1360C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319881 | ||||||
| chr16:31319898
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1708-1343C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319898 | ||||||
| chr16:31319923
|
C | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-1318C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31319923 | ||||||
| chr16:31320002
|
T | C | 79 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(76): Show | 80 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1708-1239T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31320002 | ||||||
| chr16:31320054
|
C | T | 1 | a0001c0007t0004g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1708-1187C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31320054 | ||||||
| chr16:31320189
|
A | G | 1 | a0002c0003t0003g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1708-1052A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31320189 | ||||||
| chr16:31320637
|
C | T | 62 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(59): Show | 62 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1708-604C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31320637 | ||||||
| chr16:31321019
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-222T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31321019 | ||||||
| chr16:31321024
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1708-217T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31321024 | ||||||
| chr16:31321038
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1708-203G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31321038 | ||||||
| chr16:31321123
|
G | C | 1 | a0001c0002t0002g0021 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1708-118G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 14/29 | chr16 | 31321123 | ||||||
| chr16:31321677
|
A | G | 3 | a0003c0004t0005g0025a0003c0004t0005g0027a0003c0004t0006g0034 | 3 | HG01109.hp2 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2002+50A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31321677 | ||||||
| chr16:31321769
|
G | C | 5 | a0001c0007t0004g0143a0001c0007t0004g0144a0001c0007t0004g0145others(2): Show | 5 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2002+142G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31321769 | ||||||
| chr16:31321822
|
G | A | 1 | a0009c0014t0001g0225 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2002+195G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31321822 | ||||||
| chr16:31322311
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2002+684G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322311 | ||||||
| chr16:31322402
|
G | A | 6 | a0002c0003t0003g0122a0002c0003t0003g0123a0002c0003t0003g0124others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2002+775G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322402 | ||||||
| chr16:31322440
|
C | T | 1 | a0001c0002t0002g0035 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2002+813C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322440 | ||||||
| chr16:31322819
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2002+1192G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322819 | ||||||
| chr16:31322872
|
G | A | 1 | a0004c0006t0003g0004 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2002+1245G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322872 | ||||||
| chr16:31322915
|
C | A | 61 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(58): Show | 61 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2002+1288C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31322915 | ||||||
| chr16:31323244
|
C | A | 1 | a0004c0006t0003g0012 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2003-1155C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323244 | ||||||
| chr16:31323300
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2003-1099T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323300 | ||||||
| chr16:31323361
|
T | G | 166 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(163): Show | 167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2003-1038T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323361 | ||||||
| chr16:31323426
|
C | CA | 15 | a0001c0001t0001g0236a0001c0001t0004g0147a0001c0005t0004g0001others(12): Show | 16 | HG01175.hp1 HG02258.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2003-956dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31323426 | |||||
| chr16:31323426
|
CA | C | 10 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(7): Show | 10 | HG00099.hp2 HG00642.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2003-956delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31323426 | |||||
| chr16:31323524
|
G | A | 1 | a0001c0002t0002g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2003-875G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323524 | ||||||
| chr16:31323544
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2003-855G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323544 | ||||||
| chr16:31323681
|
T | G | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2003-718T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323681 | ||||||
| chr16:31323691
|
T | G | 2 | a0002c0003t0003g0074a0002c0003t0003g0088 | 2 | HG02071.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2003-708T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323691 | ||||||
| chr16:31323702
|
G | A | 6 | a0002c0003t0003g0122a0002c0003t0003g0123a0002c0003t0003g0124others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003-697G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323702 | ||||||
| chr16:31323873
|
C | T | 1 | a0003c0004t0005g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2003-526C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323873 | ||||||
| chr16:31323896
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2003-503C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323896 | ||||||
| chr16:31323938
|
G | C | 1 | a0006c0010t0004g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2003-461G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323938 | ||||||
| chr16:31323939
|
G | A | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2003-460G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31323939 | ||||||
| chr16:31324013
|
A | G | 1 | a0001c0002t0002g0090 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2003-386A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31324013 | ||||||
| chr16:31324148
|
A | G | 1 | a0003c0004t0005g0019 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2003-251A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | chr16 | 31324148 | ||||||
| chr16:31324192
|
AAAGG | A | 7 | a0001c0001t0001g0217a0001c0001t0001g0236a0001c0007t0004g0143others(4): Show | 7 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003-192_2003-189d others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr16 | 31324192 | |||||
| chr16:31324585
|
T | C | 83 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(80): Show | 84 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.2157+32T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 17/29 | chr16 | 31324585 | ||||||
| chr16:31325067
|
GGACCCGT others(5): Show |
G | 21 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0005t0004g0001others(18): Show | 22 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2363+43_2363+54del others(12): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr16 | 31325067 | |||||
| chr16:31325116
|
C | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0223a0008c0015t0001g0172 | 3 | HG03669.hp2 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2363+85C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | chr16 | 31325116 | ||||||
| chr16:31325180
|
T | C | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2364-83T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | chr16 | 31325180 | ||||||
| chr16:31325198
|
T | C | 167 | a0001c0001t0001g0193a0001c0001t0002g0076a0001c0001t0002g0131others(164): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.2364-65T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | chr16 | 31325198 | ||||||
| chr16:31325202
|
G | A | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2364-61G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 19/29 | chr16 | 31325202 | ||||||
| chr16:31325697
|
T | C | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2628+75T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31325697 | ||||||
| chr16:31325834
|
G | A | 38 | a0002c0003t0003g0016a0002c0003t0003g0060a0002c0003t0003g0061others(35): Show | 38 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.2628+212G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31325834 | ||||||
| chr16:31325846
|
G | A | 1 | a0001c0002t0002g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2628+224G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31325846 | ||||||
| chr16:31325927
|
G | A | 32 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(29): Show | 33 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.2628+305G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31325927 | ||||||
| chr16:31326016
|
T | G | 9 | a0002c0003t0003g0016a0002c0003t0003g0122a0002c0003t0003g0123others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2628+394T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326016 | ||||||
| chr16:31326093
|
AAT | A | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2628+473_2628+474d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr16 | 31326093 | |||||
| chr16:31326207
|
C | T | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2628+585C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326207 | ||||||
| chr16:31326210
|
C | G | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2628+588C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326210 | ||||||
| chr16:31326356
|
A | G | 59 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(56): Show | 59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2629-500A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326356 | ||||||
| chr16:31326707
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2629-149G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 21/29 | chr16 | 31326707 | ||||||
| chr16:31327106
|
T | G | 1 | a0004c0006t0003g0015 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2708+171T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327106 | ||||||
| chr16:31327326
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2708+391C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327326 | ||||||
| chr16:31327370
|
C | G | 8 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(5): Show | 8 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2708+435C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327370 | ||||||
| chr16:31327423
|
C | CA | 58 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0064others(55): Show | 58 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.2708+501dupA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327423 | |||||
| chr16:31327423
|
C | CAA | 40 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0118others(37): Show | 40 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.2708+500_2708+501d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327423 | |||||
| chr16:31327423
|
C | CAAA | 6 | a0002c0003t0003g0016a0002c0003t0003g0110a0002c0003t0003g0113others(3): Show | 6 | HG00741.hp2 HG01106.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2708+499_2708+501d others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327423 | |||||
| chr16:31327423
|
CA | C | 14 | a0001c0001t0002g0174a0001c0007t0004g0023a0001c0007t0004g0024others(11): Show | 14 | HG01496.hp2 HG01891.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.2708+501delA | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327423 | |||||
| chr16:31327617
|
A | G | 135 | a0001c0001t0002g0174a0001c0002t0002g0021a0001c0002t0002g0026others(132): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.2709-530A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327617 | ||||||
| chr16:31327619
|
T | TAATAAA | 14 | a0001c0005t0004g0001a0001c0005t0004g0149a0001c0005t0004g0150others(11): Show | 15 | HG02109.hp1 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2709-526_2709-525i others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327619 | |||||
| chr16:31327619
|
T | TAATAATA others(2): Show |
5 | a0001c0005t0004g0156a0001c0005t0004g0157a0001c0005t0004g0158others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2709-526_2709-525i others(11): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr16 | 31327619 | |||||
| chr16:31327622
|
A | T | 1 | a0001c0001t0004g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2709-525A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327622 | ||||||
| chr16:31327729
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2709-418A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327729 | ||||||
| chr16:31327793
|
A | G | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2709-354A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327793 | ||||||
| chr16:31327952
|
A | T | 1 | a0001c0007t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2709-195A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 22/29 | chr16 | 31327952 | ||||||
| chr16:31328304
|
G | A | 59 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(56): Show | 59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2792+74G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328304 | ||||||
| chr16:31328383
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2792+153G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328383 | ||||||
| chr16:31328440
|
A | C | 2 | a0001c0001t0002g0174a0001c0013t0008g0175 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2792+210A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328440 | ||||||
| chr16:31328549
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0235 | 2 | NA18945.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2792+319G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328549 | ||||||
| chr16:31328582
|
T | C | 65 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(62): Show | 65 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2792+352T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328582 | ||||||
| chr16:31328589
|
A | ATG | 11 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(8): Show | 11 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2792+368_2792+369d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31328589 | |||||
| chr16:31328704
|
G | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2792+474G>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328704 | ||||||
| chr16:31328756
|
A | G | 2 | a0001c0005t0004g0157a0001c0005t0004g0159 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2793-472A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328756 | ||||||
| chr16:31328765
|
C | T | 49 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(46): Show | 49 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2793-463C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328765 | ||||||
| chr16:31328766
|
G | A | 1 | a0001c0002t0002g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2793-462G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328766 | ||||||
| chr16:31328772
|
G | A | 20 | a0001c0001t0004g0147a0001c0005t0004g0001a0001c0005t0004g0149others(17): Show | 21 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2793-456G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328772 | ||||||
| chr16:31328792
|
ATG | A | 153 | a0001c0001t0002g0174a0001c0002t0002g0021a0001c0002t0002g0026others(150): Show | 154 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.2793-425_2793-424d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr16 | 31328792 | |||||
| chr16:31328895
|
C | T | 86 | a0001c0001t0002g0174a0001c0002t0002g0021a0001c0002t0002g0026others(83): Show | 86 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2793-333C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328895 | ||||||
| chr16:31328896
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2793-332G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328896 | ||||||
| chr16:31328957
|
C | T | 2 | a0001c0001t0004g0114a0001c0001t0004g0115 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2793-271C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31328957 | ||||||
| chr16:31329047
|
G | A | 84 | a0001c0001t0002g0174a0001c0002t0002g0021a0001c0002t0002g0026others(81): Show | 84 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.2793-181G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31329047 | ||||||
| chr16:31329189
|
C | T | 2 | a0001c0008t0004g0140a0001c0008t0004g0141 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2793-39C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31329189 | ||||||
| chr16:31329199
|
C | T | 4 | a0001c0002t0002g0040a0001c0002t0002g0083a0001c0002t0002g0197others(1): Show | 4 | HG00544.hp2 HG01934.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2793-29C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 23/29 | chr16 | 31329199 | ||||||
| chr16:31329392
|
C | T | 11 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(8): Show | 11 | HG01496.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2868+89C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 24/29 | chr16 | 31329392 | ||||||
| chr16:31329511
|
C | T | 2 | a0001c0007t0009g0142a0007c0011t0004g0017 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2868+208C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 24/29 | chr16 | 31329511 | ||||||
| chr16:31329588
|
T | C | 167 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(164): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.2869-210T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 24/29 | chr16 | 31329588 | ||||||
| chr16:31329676
|
C | T | 51 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(48): Show | 51 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2869-122C>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 24/29 | chr16 | 31329676 | ||||||
| chr16:31330206
|
A | T | 1 | a0001c0002t0002g0168 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3060+42A>T | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 26/29 | chr16 | 31330206 | ||||||
| chr16:31330613
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | splice_region_variant&intron_variant | LOW | c.3276+8T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330613 | ||||||
| chr16:31330645
|
G | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0177a0001c0001t0001g0237 | 3 | HG01516.hp2 HG01517.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3276+40G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330645 | ||||||
| chr16:31330772
|
A | G | 2 | a0002c0003t0003g0110a0002c0003t0003g0113 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3276+167A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330772 | ||||||
| chr16:31330799
|
C | G | 59 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(56): Show | 59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3276+194C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330799 | ||||||
| chr16:31330803
|
G | C | 59 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(56): Show | 59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3276+198G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330803 | ||||||
| chr16:31330805
|
C | G | 59 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(56): Show | 59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3276+200C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330805 | ||||||
| chr16:31330807
|
G | C | 59 | a0001c0002t0002g0021a0001c0002t0002g0026a0001c0002t0002g0029others(56): Show | 59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3276+202G>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330807 | ||||||
| chr16:31330807
|
G | GAC | 86 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(83): Show | 86 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.3276+204_3276+205d others(4): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr16 | 31330807 | |||||
| chr16:31330824
|
T | G | 1 | a0009c0014t0001g0225 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3276+219T>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31330824 | ||||||
| chr16:31330874
|
T | TAGAG | 164 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(161): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3276+272_3276+273i others(6): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr16 | 31330874 | |||||
| chr16:31330925
|
AGACAGT | A | 51 | a0001c0007t0004g0023a0001c0007t0004g0024a0001c0007t0004g0109others(48): Show | 51 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.3277-237_3277-232d others(8): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr16 | 31330925 | |||||
| chr16:31331017
|
G | A | 1 | a0001c0002t0007g0030 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3277-148G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31331017 | ||||||
| chr16:31331096
|
C | A | 1 | a0001c0002t0002g0041 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3277-69C>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 28/29 | chr16 | 31331096 | ||||||
| chr16:31331287
|
T | C | 233 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.3387+12T>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331287 | ||||||
| chr16:31331295
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3387+20C>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331295 | ||||||
| chr16:31331407
|
A | C | 1 | a0001c0007t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3387+132A>C | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331407 | ||||||
| chr16:31331467
|
C | CTTG | 94 | a0001c0001t0002g0076a0001c0001t0002g0131a0001c0001t0002g0132others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.3388-167_3388-165d others(5): Show |
ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr16 | 31331467 | |||||
| chr16:31331584
|
G | A | 1 | a0004c0006t0003g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3388-52G>A | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331584 | ||||||
| chr16:31331634
|
A | G | 1 | a0002c0003t0003g0085 | 1 | HG03491.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.3388-2A>G | ITGAM | ENSG00000169896.18 | transcript | ENST00000544665.9 | protein_coding | 29/29 | chr16 | 31331634 |