Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 341346 |
|---|---|
| ensemblid | ENSG00000165935.10 |
| hgncid | 34448 |
| symbol | SMCO2 |
| name | single-pass membrane protein with coiled-coil domains 2 |
| refseq_nuc | NM_001395208.2 |
| refseq_prot | NP_001382137.1 |
| ensembl_nuc | ENST00000535986.2 |
| ensembl_prot | ENSP00000441688.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 27446736 |
| end | 27502185 |
| strand | + |
| ver | v1.2 |
| region | chr12:27446736-27502185 |
| region5000 | chr12:27441736-27507185 |
| regionname0 | SMCO2_chr12_27446736_27502185 |
| regionname5000 | SMCO2_chr12_27441736_27507185 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 21 | 13 | 2 | 3 | 1 | 2 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001 | 1/1 | 343 | 177 | 31 | 40 | 69 | 12 | 23 | 52 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002 | 0/0 | 343 | 80 | 35 | 5 | 35 | 1 | 4 | 30 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003 | 0/0 | 343 | 72 | 6 | 4 | 49 | 0 | 13 | 40 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0004 | 0/0 | 343 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0005 | 0/0 | 343 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0006 | 0/0 | 343 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0007 | 0/0 | 343 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0008 | 0/0 | 343 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1032 | 144 | 25 | 27 | 66 | 6 | 19 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0002 | 0/0 | 1032 | 67 | 2 | 4 | 48 | 0 | 13 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0003 | 0/0 | 1032 | 47 | 5 | 2 | 35 | 1 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0004 | 0/0 | 1032 | 22 | 6 | 9 | 1 | 2 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0005 | 0/0 | 1032 | 18 | 16 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0006 | 0/0 | 657 | 13 | 10 | 2 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0007 | 0/0 | 1032 | 9 | 8 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0008 | 1/0 | 1032 | 9 | 0 | 4 | 0 | 4 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0009 | 0/0 | 1032 | 5 | 4 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0010 | 0/0 | 657 | 5 | 0 | 0 | 3 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0011 | 0/0 | 1032 | 4 | 1 | 1 | 0 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0012 | 0/0 | 1032 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0013 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0014 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0015 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0016 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0017 | 0/0 | 657 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0018 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0019 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0020 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0021 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| c0022 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 165 | 151 | 55 | 33 | 38 | 8 | 17 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| t0002 | 1/1 | 165 | 122 | 8 | 12 | 79 | 4 | 17 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| t0003 | 0/0 | 165 | 42 | 2 | 1 | 35 | 0 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| t0004 | 0/0 | 165 | 24 | 14 | 4 | 1 | 1 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| t0005 | 0/0 | 101 | 12 | 12 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| t0006 | 0/0 | 101 | 9 | 1 | 2 | 3 | 1 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0002 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0006 | 0/0 | 657 | 13 | 10 | 2 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0000c0010 | 0/0 | 657 | 5 | 0 | 0 | 3 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0000c0017 | 0/0 | 657 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0000c0022 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0001 | 0/1 | 1032 | 144 | 25 | 27 | 66 | 6 | 19 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0004 | 0/0 | 1032 | 22 | 6 | 9 | 1 | 2 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0008 | 1/0 | 1032 | 9 | 0 | 4 | 0 | 4 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0012 | 0/0 | 1032 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0003 | 0/0 | 1032 | 47 | 5 | 2 | 35 | 1 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0005 | 0/0 | 1032 | 18 | 16 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0007 | 0/0 | 1032 | 9 | 8 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0015 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0016 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0019 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0021 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003c0002 | 0/0 | 1032 | 67 | 2 | 4 | 48 | 0 | 13 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003c0009 | 0/0 | 1032 | 5 | 4 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0004c0011 | 0/0 | 1032 | 4 | 1 | 1 | 0 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0005c0014 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0006c0013 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0007c0020 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0008c0018 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0006t0005 | 0/0 | 757 | 10 | 10 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0000c0006t0006 | 0/0 | 757 | 3 | 0 | 2 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0000c0010t0006 | 0/0 | 757 | 5 | 0 | 0 | 3 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0000c0017t0005 | 0/0 | 757 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0000c0022t0006 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0001t0001 | 0/0 | 1196 | 101 | 22 | 24 | 35 | 6 | 14 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0001t0002 | 0/1 | 1196 | 42 | 3 | 3 | 31 | 0 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0001t0004 | 0/0 | 1196 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0004t0001 | 0/0 | 1196 | 17 | 6 | 6 | 0 | 2 | 3 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0004t0002 | 0/0 | 1196 | 3 | 0 | 1 | 1 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0004t0004 | 0/0 | 1196 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0008t0002 | 1/0 | 1196 | 9 | 0 | 4 | 0 | 4 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0001c0012t0001 | 0/0 | 1196 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0003t0001 | 0/0 | 1196 | 6 | 5 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0003t0003 | 0/0 | 1196 | 39 | 0 | 1 | 34 | 0 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0003t0004 | 0/0 | 1196 | 2 | 0 | 0 | 1 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0005t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0005t0002 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0005t0003 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0005t0004 | 0/0 | 1196 | 14 | 12 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0007t0001 | 0/0 | 1196 | 9 | 8 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0015t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0016t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0019t0004 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0002c0021t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003c0002t0001 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003c0002t0002 | 0/0 | 1196 | 63 | 2 | 4 | 47 | 0 | 10 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003c0002t0004 | 0/0 | 1196 | 3 | 0 | 0 | 0 | 0 | 3 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003c0009t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003c0009t0003 | 0/0 | 1196 | 2 | 1 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0003c0009t0004 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0004c0011t0001 | 0/0 | 1196 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0004c0011t0002 | 0/0 | 1196 | 3 | 1 | 0 | 0 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0005c0014t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0006c0013t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0006c0013t0002 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0007c0020t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| a0008c0018t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | copy fasta | chr12 | 27441736 | 27507185 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0006t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0006g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0006t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0010t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0010t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0010t0006g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0010t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0010t0006g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0017t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0017t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0000c0022t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0004t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0008t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0012t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0012t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0005t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0015t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0015t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0016t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0016t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0019t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0021t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0009t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0009t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0009t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0009t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0009t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0004c0011t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0004c0011t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0004c0011t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0005c0014t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0005c0014t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0006c0013t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0006c0013t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0007c0020t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0008c0018t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0162 | EUR | GBR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00099 | hp2 | a0000 | c0006 | t0006 | g0033 | EUR | GBR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00140 | hp2 | a0001 | c0008 | t0002 | g0051 | EUR | GBR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00280 | hp1 | a0001 | c0008 | t0002 | g0047 | EUR | FIN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | FIN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00323 | hp1 | a0001 | c0008 | t0002 | g0049 | EUR | FIN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00323 | hp2 | a0001 | c0004 | t0001 | g0213 | EUR | FIN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00438 | hp2 | a0002 | c0003 | t0003 | g0148 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00544 | hp1 | a0003 | c0002 | t0002 | g0123 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00558 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00558 | hp2 | a0003 | c0002 | t0002 | g0124 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00609 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0233 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00673 | hp2 | a0001 | c0004 | t0002 | g0322 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00733 | hp2 | a0003 | c0002 | t0002 | g0053 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00741 | hp2 | a0002 | c0007 | t0001 | g0029 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01069 | hp1 | a0001 | c0008 | t0002 | g0046 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01069 | hp2 | a0000 | c0006 | t0006 | g0006 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01070 | hp1 | a0001 | c0008 | t0002 | g0050 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01071 | hp2 | a0000 | c0006 | t0006 | g0006 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0215 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0242 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01167 | hp2 | a0002 | c0005 | t0004 | g0304 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01168 | hp1 | a0003 | c0002 | t0002 | g0009 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01169 | hp1 | a0003 | c0002 | t0002 | g0009 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01169 | hp2 | a0002 | c0005 | t0004 | g0305 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0189 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0214 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01243 | hp2 | a0001 | c0004 | t0004 | g0269 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0324 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01258 | hp1 | a0001 | c0004 | t0001 | g0208 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01361 | hp2 | a0001 | c0008 | t0002 | g0048 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01433 | hp1 | a0001 | c0004 | t0004 | g0278 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01496 | hp2 | a0001 | c0008 | t0002 | g0044 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | IBS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01517 | hp2 | a0001 | c0008 | t0002 | g0045 | EUR | IBS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01884 | hp1 | a0002 | c0016 | t0001 | g0239 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01884 | hp2 | a0002 | c0019 | t0004 | g0295 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01891 | hp1 | a0002 | c0005 | t0004 | g0310 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0228 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0279 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01981 | hp1 | a0003 | c0002 | t0002 | g0065 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01981 | hp2 | a0001 | c0004 | t0002 | g0052 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02004 | hp1 | a0002 | c0003 | t0003 | g0143 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02015 | hp2 | a0000 | c0010 | t0006 | g0334 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02027 | hp2 | a0003 | c0009 | t0003 | g0144 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02040 | hp1 | a0003 | c0002 | t0002 | g0119 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02055 | hp1 | a0000 | c0006 | t0005 | g0166 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02055 | hp2 | a0002 | c0007 | t0001 | g0032 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02071 | hp2 | a0003 | c0002 | t0002 | g0060 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02074 | hp1 | a0003 | c0002 | t0002 | g0059 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0131 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02132 | hp1 | a0003 | c0002 | t0002 | g0117 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02145 | hp1 | a0002 | c0005 | t0004 | g0302 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02145 | hp2 | a0002 | c0007 | t0001 | g0031 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02155 | hp1 | a0003 | c0002 | t0002 | g0095 | EAS | CDX | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CDX | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02165 | hp2 | a0003 | c0002 | t0002 | g0136 | EAS | CDX | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02257 | hp1 | a0002 | c0015 | t0001 | g0313 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02257 | hp2 | a0002 | c0005 | t0004 | g0312 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02258 | hp2 | a0000 | c0006 | t0005 | g0015 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02280 | hp1 | a0003 | c0009 | t0003 | g0134 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02300 | hp2 | a0004 | c0011 | t0001 | g0274 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02572 | hp1 | a0002 | c0005 | t0004 | g0303 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02572 | hp2 | a0007 | c0020 | t0001 | g0318 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0185 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02602 | hp2 | a0003 | c0002 | t0004 | g0202 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0197 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02622 | hp1 | a0008 | c0018 | t0001 | g0267 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02622 | hp2 | a0003 | c0009 | t0001 | g0207 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02647 | hp1 | a0003 | c0009 | t0001 | g0253 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02683 | hp2 | a0003 | c0002 | t0002 | g0128 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02717 | hp2 | a0000 | c0006 | t0005 | g0289 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02723 | hp1 | a0005 | c0014 | t0001 | g0320 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02735 | hp2 | a0000 | c0010 | t0006 | g0333 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02809 | hp1 | a0002 | c0005 | t0001 | g0027 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0210 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02818 | hp1 | a0000 | c0006 | t0005 | g0294 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02818 | hp2 | a0002 | c0005 | t0004 | g0307 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02886 | hp1 | a0003 | c0002 | t0002 | g0096 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02886 | hp2 | a0002 | c0007 | t0001 | g0023 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02895 | hp1 | a0000 | c0006 | t0005 | g0293 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02896 | hp2 | a0002 | c0005 | t0004 | g0308 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02897 | hp1 | a0002 | c0005 | t0004 | g0309 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02922 | hp1 | a0002 | c0007 | t0001 | g0025 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0235 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02965 | hp1 | a0000 | c0006 | t0005 | g0167 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02965 | hp2 | a0002 | c0005 | t0004 | g0300 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02970 | hp1 | a0002 | c0007 | t0001 | g0022 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02976 | hp1 | a0002 | c0007 | t0001 | g0028 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02976 | hp2 | a0000 | c0017 | t0005 | g0020 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03017 | hp2 | a0000 | c0010 | t0006 | g0335 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03041 | hp1 | a0001 | c0004 | t0001 | g0240 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03041 | hp2 | a0005 | c0014 | t0001 | g0321 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03098 | hp1 | a0002 | c0005 | t0004 | g0280 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03098 | hp2 | a0002 | c0005 | t0001 | g0018 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03139 | hp1 | a0002 | c0015 | t0001 | g0314 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03195 | hp1 | a0002 | c0016 | t0001 | g0315 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03195 | hp2 | a0002 | c0021 | t0001 | g0019 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03209 | hp1 | a0006 | c0013 | t0002 | g0330 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03209 | hp2 | a0000 | c0017 | t0005 | g0024 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03225 | hp1 | a0002 | c0007 | t0001 | g0021 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03225 | hp2 | a0006 | c0013 | t0001 | g0323 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03239 | hp1 | a0003 | c0002 | t0002 | g0098 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03239 | hp2 | a0002 | c0003 | t0003 | g0153 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03453 | hp1 | a0002 | c0005 | t0004 | g0306 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03491 | hp2 | a0004 | c0011 | t0002 | g0017 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03492 | hp1 | a0003 | c0002 | t0002 | g0104 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03492 | hp2 | a0004 | c0011 | t0002 | g0017 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03516 | hp1 | a0000 | c0006 | t0005 | g0291 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03516 | hp2 | a0002 | c0005 | t0004 | g0311 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0234 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03654 | hp2 | a0003 | c0002 | t0002 | g0127 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03688 | hp2 | a0002 | c0003 | t0003 | g0154 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03704 | hp1 | a0003 | c0002 | t0004 | g0203 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03831 | hp1 | a0002 | c0003 | t0003 | g0155 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03831 | hp2 | a0003 | c0002 | t0002 | g0101 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03834 | hp1 | a0002 | c0003 | t0003 | g0161 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03927 | hp2 | a0003 | c0002 | t0002 | g0103 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03942 | hp2 | a0003 | c0002 | t0002 | g0099 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04115 | hp1 | a0003 | c0002 | t0004 | g0195 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0264 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04184 | hp1 | a0001 | c0004 | t0002 | g0087 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0270 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04204 | hp2 | a0003 | c0002 | t0002 | g0106 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04228 | hp2 | a0003 | c0002 | t0002 | g0115 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0209 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CHB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0084 | EAS | CHB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18747 | hp2 | a0001 | c0012 | t0001 | g0034 | EAS | CHB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18906 | hp2 | a0002 | c0007 | t0001 | g0026 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18939 | hp1 | a0002 | c0003 | t0003 | g0151 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18940 | hp1 | a0003 | c0002 | t0002 | g0066 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18940 | hp2 | a0002 | c0003 | t0003 | g0317 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18941 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18942 | hp1 | a0002 | c0003 | t0003 | g0138 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18942 | hp2 | a0003 | c0002 | t0002 | g0129 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18944 | hp1 | a0002 | c0003 | t0003 | g0135 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18945 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18948 | hp2 | a0003 | c0002 | t0002 | g0008 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18949 | hp1 | a0003 | c0002 | t0002 | g0056 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18951 | hp2 | a0003 | c0002 | t0002 | g0091 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18952 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18959 | hp1 | a0003 | c0002 | t0002 | g0094 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18959 | hp2 | a0002 | c0003 | t0003 | g0140 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0146 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18961 | hp2 | a0002 | c0003 | t0003 | g0130 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18962 | hp1 | a0002 | c0003 | t0004 | g0176 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18962 | hp2 | a0002 | c0003 | t0003 | g0137 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18966 | hp2 | a0003 | c0002 | t0002 | g0092 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18968 | hp1 | a0003 | c0002 | t0002 | g0093 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18968 | hp2 | a0002 | c0003 | t0003 | g0152 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18969 | hp1 | a0003 | c0002 | t0002 | g0102 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18970 | hp1 | a0002 | c0003 | t0003 | g0316 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18971 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18973 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18975 | hp2 | a0003 | c0002 | t0002 | g0067 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18977 | hp2 | a0003 | c0002 | t0002 | g0105 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18978 | hp1 | a0003 | c0002 | t0002 | g0109 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18979 | hp2 | a0003 | c0002 | t0002 | g0126 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18980 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18981 | hp1 | a0003 | c0002 | t0002 | g0008 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18983 | hp2 | a0002 | c0003 | t0003 | g0142 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18985 | hp2 | a0003 | c0002 | t0002 | g0111 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0157 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18986 | hp2 | a0000 | c0010 | t0006 | g0332 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18988 | hp1 | a0002 | c0003 | t0003 | g0133 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18988 | hp2 | a0003 | c0002 | t0002 | g0114 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18989 | hp1 | a0003 | c0002 | t0002 | g0068 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18989 | hp2 | a0002 | c0003 | t0003 | g0145 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18990 | hp1 | a0003 | c0002 | t0002 | g0090 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18990 | hp2 | a0002 | c0003 | t0003 | g0149 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18991 | hp1 | a0003 | c0002 | t0002 | g0107 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18992 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18995 | hp2 | a0003 | c0002 | t0002 | g0089 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18998 | hp1 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19002 | hp2 | a0002 | c0003 | t0003 | g0159 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19003 | hp1 | a0003 | c0002 | t0002 | g0125 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0150 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19005 | hp1 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19005 | hp2 | a0002 | c0003 | t0003 | g0132 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19007 | hp1 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19007 | hp2 | a0003 | c0002 | t0002 | g0113 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19010 | hp2 | a0003 | c0002 | t0002 | g0088 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19011 | hp1 | a0000 | c0010 | t0006 | g0238 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19012 | hp1 | a0003 | c0002 | t0002 | g0010 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19012 | hp2 | a0001 | c0012 | t0001 | g0211 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19030 | hp1 | a0003 | c0002 | t0002 | g0097 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19043 | hp2 | a0002 | c0005 | t0002 | g0120 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19054 | hp2 | a0003 | c0002 | t0002 | g0010 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19055 | hp2 | a0002 | c0003 | t0003 | g0158 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19058 | hp2 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19063 | hp2 | a0002 | c0003 | t0003 | g0139 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19066 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19072 | hp2 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19078 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19080 | hp1 | a0003 | c0002 | t0002 | g0108 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19081 | hp2 | a0003 | c0002 | t0002 | g0112 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19082 | hp1 | a0003 | c0002 | t0002 | g0141 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19084 | hp1 | a0003 | c0002 | t0002 | g0078 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19085 | hp2 | a0002 | c0003 | t0003 | g0156 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19086 | hp2 | a0003 | c0002 | t0001 | g0249 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19087 | hp1 | a0002 | c0003 | t0003 | g0160 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19090 | hp1 | a0003 | c0002 | t0002 | g0118 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19091 | hp1 | a0003 | c0002 | t0002 | g0057 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19091 | hp2 | a0002 | c0003 | t0003 | g0147 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19240 | hp1 | a0000 | c0006 | t0005 | g0292 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0190 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20129 | hp1 | a0000 | c0022 | t0006 | g0030 | AFR | ASW | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20129 | hp2 | a0002 | c0005 | t0004 | g0301 | AFR | ASW | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20752 | hp1 | a0002 | c0003 | t0004 | g0268 | EUR | TSI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | TSI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0212 | SAS | GIH | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20905 | hp2 | a0003 | c0002 | t0002 | g0116 | SAS | GIH | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0204 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02486 | hp1 | a0004 | c0011 | t0002 | g0328 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03471 | hp1 | a0002 | c0005 | t0003 | g0329 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03471 | hp2 | a0000 | c0006 | t0005 | g0290 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | USA | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | USA | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0191 | AFR | USA | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20300 | hp2 | a0000 | c0006 | t0005 | g0015 | AFR | USA | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA21309 | hp1 | a0003 | c0009 | t0004 | g0172 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0288 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0250 | REF | REF | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| homoSapiens_grch38 | hp1 | a0001 | c0008 | t0002 | g0035 | REF | REF | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27472846
|
G | A | 1 | a0008 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.205G>A | p.Glu69Lys | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/9 | 305/1196 | 205/1032 | 69/343 | chr12 | 27472846 | ||
| chr12:27475674
|
C | T | 2 | a0000a0007 | 6 | HG02015.hp2 HG02572.hp2 HG02735.hp2 others(3): Show |
missense_variant | MODERATE | c.455C>T | p.Thr152Met | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/9 | 555/1196 | 455/1032 | 152/343 | chr12 | 27475674 | ||
| chr12:27475679
|
A | G | 1 | a0005 | 2 | HG02723.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.460A>G | p.Lys154Glu | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/9 | 560/1196 | 460/1032 | 154/343 | chr12 | 27475679 | ||
| chr12:27488540
|
G | A | 4 | a0000a0002a0003others(1): Show | 175 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
missense_variant | MODERATE | c.593G>A | p.Ser198Asn | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/9 | 693/1196 | 593/1032 | 198/343 | chr12 | 27488540 | ||
| chr12:27495209
|
GTTTTCTC others(7014): Show |
G | 1 | a0000 | 21 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
exon_loss_variant | HIGH | c.658-470_*109del | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | chr12 | 27495209 | ||||||
| chr12:27495777
|
C | T | 3 | a0003a0004a0006 | 78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
missense_variant | MODERATE | c.755C>T | p.Thr252Met | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | 855/1196 | 755/1032 | 252/343 | chr12 | 27495777 | ||
| chr12:27502065
|
C | T | 1 | a0006 | 2 | HG03209.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.976C>T | p.Arg326Trp | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 9/9 | 1076/1196 | 976/1032 | 326/343 | chr12 | 27502065 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27474822
|
C | T | 1 | a0000c0022 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.271C>T | p.Leu91Leu | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/9 | 371/1196 | 271/1032 | 91/343 | chr12 | 27474822 | ||
| chr12:27474872
|
G | A | 14 | a0000c0006a0001c0001a0001c0004others(11): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
synonymous_variant | LOW | c.321G>A | p.Ala107Ala | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/9 | 421/1196 | 321/1032 | 107/343 | chr12 | 27474872 | ||
| chr12:27475588
|
G | C | 2 | a0000c0017a0002c0021 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.369G>C | p.Leu123Leu | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/9 | 469/1196 | 369/1032 | 123/343 | chr12 | 27475588 | ||
| chr12:27475594
|
C | T | 2 | a0002c0015a0002c0016 | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.375C>T | p.Gly125Gly | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/9 | 475/1196 | 375/1032 | 125/343 | chr12 | 27475594 | ||
| chr12:27488532
|
A | G | 2 | a0000c0017a0002c0021 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.585A>G | p.Gln195Gln | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/9 | 685/1196 | 585/1032 | 195/343 | chr12 | 27488532 | ||
| chr12:27495727
|
T | C | 1 | a0002c0019 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.705T>C | p.Tyr235Tyr | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | 805/1196 | 705/1032 | 235/343 | chr12 | 27495727 | ||
| chr12:27495844
|
C | T | 3 | a0001c0012a0002c0003a0002c0016 | 51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
synonymous_variant | LOW | c.822C>T | p.Arg274Arg | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | 922/1196 | 822/1032 | 274/343 | chr12 | 27495844 | ||
| chr12:27495853
|
A | G | 10 | a0001c0012a0002c0003a0002c0005others(7): Show | 150 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(147): Show |
splice_region_variant&synonymous_variant | LOW | c.831A>G | p.Ala277Ala | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | 931/1196 | 831/1032 | 277/343 | chr12 | 27495853 | ||
| chr12:27501965
|
C | T | 1 | a0001c0004 | 22 | HG00099.hp1 HG00323.hp2 HG00673.hp2 others(19): Show |
synonymous_variant | LOW | c.876C>T | p.Thr292Thr | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 9/9 | 976/1196 | 876/1032 | 292/343 | chr12 | 27501965 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27446766
|
G | T | 28 | a0000c0006t0005a0000c0006t0006a0000c0010t0006others(25): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/9 | 23866 | chr12 | 27446766 | |||||
| chr12:27446770
|
T | C | 28 | a0000c0006t0005a0000c0006t0006a0000c0010t0006others(25): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/9 | chr12 | 27446770 | ||||||
| chr12:27470625
|
C | T | 13 | a0000c0006t0006a0000c0010t0006a0000c0022t0006others(10): Show | 75 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/9 | chr12 | 27470625 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27446836
|
G | T | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+11G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27446836 | ||||||
| chr12:27447001
|
G | A | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11+176G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447001 | ||||||
| chr12:27447035
|
G | T | 1 | a0001c0001t0002g0331 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+210G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447035 | ||||||
| chr12:27447043
|
G | T | 9 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0001t0002g0326others(6): Show | 10 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+218G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447043 | ||||||
| chr12:27447084
|
A | T | 1 | a0001c0004t0002g0322 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-11+259A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447084 | ||||||
| chr12:27447227
|
G | C | 21 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0010t0006g0332others(18): Show | 22 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11+402G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447227 | ||||||
| chr12:27447349
|
C | A | 1 | a0001c0012t0001g0034 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-11+524C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447349 | ||||||
| chr12:27447384
|
C | T | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+559C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447384 | ||||||
| chr12:27447398
|
C | T | 281 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(278): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-11+573C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447398 | ||||||
| chr12:27447418
|
G | T | 334 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(331): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-11+593G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447418 | ||||||
| chr12:27447437
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-11+612G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447437 | ||||||
| chr12:27447450
|
C | T | 2 | a0001c0001t0001g0319a0007c0020t0001g0318 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-11+625C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447450 | ||||||
| chr12:27447547
|
C | T | 2 | a0002c0003t0003g0316a0002c0003t0003g0317 | 2 | NA18940.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-11+722C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447547 | ||||||
| chr12:27447554
|
C | T | 187 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(184): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.-11+729C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447554 | ||||||
| chr12:27447614
|
T | C | 172 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(169): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-11+789T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447614 | ||||||
| chr12:27447728
|
CA | C | 217 | a0000c0006t0005g0015a0000c0006t0005g0289a0000c0006t0005g0290others(214): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.-11+920delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27447728 | |||||
| chr12:27447760
|
C | G | 7 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(4): Show | 7 | HG00544.hp2 NA18747.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+935C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447760 | ||||||
| chr12:27447776
|
T | TG | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+952dupG | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27447776 | |||||
| chr12:27447896
|
G | C | 166 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(163): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-11+1071G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447896 | ||||||
| chr12:27447906
|
C | T | 170 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(167): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-11+1081C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447906 | ||||||
| chr12:27448132
|
G | A | 3 | a0000c0022t0006g0030a0002c0007t0001g0031a0002c0007t0001g0032 | 3 | HG02055.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-11+1307G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448132 | ||||||
| chr12:27448350
|
G | A | 8 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(5): Show | 8 | HG01975.hp2 HG02155.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+1525G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448350 | ||||||
| chr12:27448460
|
C | T | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1635C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448460 | ||||||
| chr12:27448488
|
A | G | 12 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0001t0002g0326others(9): Show | 13 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+1663A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448488 | ||||||
| chr12:27448503
|
T | C | 12 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+1678T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448503 | ||||||
| chr12:27448538
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-11+1713C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448538 | ||||||
| chr12:27448903
|
G | T | 1 | a0001c0001t0001g0016 | 2 | HG01192.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-11+2078G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448903 | ||||||
| chr12:27448992
|
C | T | 12 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+2167C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448992 | ||||||
| chr12:27449024
|
A | C | 10 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+2199A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449024 | ||||||
| chr12:27449190
|
A | G | 234 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(231): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-11+2365A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449190 | ||||||
| chr12:27449207
|
G | A | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+2382G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449207 | ||||||
| chr12:27449252
|
G | A | 182 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(179): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-11+2427G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449252 | ||||||
| chr12:27449315
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-11+2490T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449315 | ||||||
| chr12:27449341
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-11+2516G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449341 | ||||||
| chr12:27449880
|
G | A | 9 | a0000c0017t0005g0024a0002c0005t0001g0027a0002c0007t0001g0021others(6): Show | 9 | HG00741.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+3055G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449880 | ||||||
| chr12:27449930
|
C | T | 1 | a0003c0002t0002g0078 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-11+3105C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449930 | ||||||
| chr12:27449954
|
G | T | 43 | a0001c0001t0002g0007a0001c0001t0002g0036a0001c0001t0002g0037others(40): Show | 45 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11+3129G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449954 | ||||||
| chr12:27449991
|
G | A | 1 | a0002c0003t0003g0130 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-11+3166G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449991 | ||||||
| chr12:27450307
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-11+3482C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450307 | ||||||
| chr12:27450308
|
A | G | 234 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(231): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-11+3483A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450308 | ||||||
| chr12:27450421
|
A | C | 1 | a0001c0001t0001g0297 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-11+3596A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450421 | ||||||
| chr12:27450521
|
G | A | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11+3696G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450521 | ||||||
| chr12:27450566
|
C | G | 1 | a0001c0001t0001g0296 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-11+3741C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450566 | ||||||
| chr12:27450608
|
G | C | 16 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11+3783G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450608 | ||||||
| chr12:27450684
|
G | A | 8 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+3859G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450684 | ||||||
| chr12:27450774
|
A | G | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+3949A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450774 | ||||||
| chr12:27451027
|
C | T | 11 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0001t0002g0326others(8): Show | 12 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+4202C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451027 | ||||||
| chr12:27451043
|
C | A | 1 | a0002c0007t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11+4218C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451043 | ||||||
| chr12:27451274
|
A | G | 1 | a0001c0004t0002g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-11+4449A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451274 | ||||||
| chr12:27451330
|
G | A | 197 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(194): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-11+4505G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451330 | ||||||
| chr12:27451332
|
A | G | 1 | a0002c0003t0003g0161 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-11+4507A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451332 | ||||||
| chr12:27451502
|
A | G | 158 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(155): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-11+4677A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451502 | ||||||
| chr12:27451693
|
C | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+4868C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451693 | ||||||
| chr12:27451703
|
C | A | 2 | a0001c0001t0002g0324a0001c0001t0002g0325 | 2 | HG01255.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+4878C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451703 | ||||||
| chr12:27451778
|
A | C | 12 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0001t0002g0326others(9): Show | 13 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+4953A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451778 | ||||||
| chr12:27451818
|
G | A | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+4993G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451818 | ||||||
| chr12:27451842
|
T | A | 168 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(165): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.-11+5017T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451842 | ||||||
| chr12:27451889
|
C | T | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+5064C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451889 | ||||||
| chr12:27452017
|
G | A | 21 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(18): Show | 24 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11+5192G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452017 | ||||||
| chr12:27452129
|
G | A | 2 | a0002c0015t0001g0313a0002c0015t0001g0314 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11+5304G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452129 | ||||||
| chr12:27452331
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-11+5506C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452331 | ||||||
| chr12:27452505
|
G | A | 11 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0001t0002g0326others(8): Show | 12 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+5680G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452505 | ||||||
| chr12:27452565
|
C | G | 10 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(7): Show | 12 | HG01192.hp1 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+5740C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452565 | ||||||
| chr12:27452572
|
C | G | 4 | a0002c0005t0004g0307a0002c0005t0004g0308a0002c0005t0004g0309others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+5747C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452572 | ||||||
| chr12:27452693
|
C | T | 13 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+5868C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452693 | ||||||
| chr12:27452853
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0281others(7): Show | 12 | HG02109.hp1 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+6028A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452853 | ||||||
| chr12:27452921
|
G | A | 13 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+6096G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452921 | ||||||
| chr12:27452925
|
C | T | 13 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+6100C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452925 | ||||||
| chr12:27453028
|
C | T | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11+6203C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453028 | ||||||
| chr12:27453055
|
A | G | 37 | a0002c0003t0003g0004a0002c0003t0003g0005a0002c0003t0003g0011others(34): Show | 42 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-11+6230A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453055 | ||||||
| chr12:27453106
|
C | T | 37 | a0002c0003t0003g0004a0002c0003t0003g0005a0002c0003t0003g0011others(34): Show | 42 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-11+6281C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453106 | ||||||
| chr12:27453136
|
T | C | 210 | a0000c0010t0006g0238a0000c0017t0005g0024a0001c0001t0001g0002others(207): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-11+6311T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453136 | ||||||
| chr12:27453357
|
G | A | 9 | a0000c0017t0005g0024a0002c0005t0001g0027a0002c0007t0001g0021others(6): Show | 9 | HG00741.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+6532G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453357 | ||||||
| chr12:27453537
|
A | G | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+6712A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453537 | ||||||
| chr12:27453626
|
C | G | 1 | a0001c0004t0001g0279 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-11+6801C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453626 | ||||||
| chr12:27453749
|
G | A | 9 | a0000c0017t0005g0024a0002c0005t0001g0027a0002c0007t0001g0021others(6): Show | 9 | HG00741.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+6924G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453749 | ||||||
| chr12:27453751
|
G | T | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+6926G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453751 | ||||||
| chr12:27453853
|
A | G | 6 | a0001c0001t0001g0165a0001c0001t0001g0275a0001c0001t0001g0276others(3): Show | 6 | HG00280.hp2 HG00738.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+7028A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453853 | ||||||
| chr12:27453868
|
T | G | 1 | a0003c0002t0002g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-11+7043T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453868 | ||||||
| chr12:27453899
|
C | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+7074C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453899 | ||||||
| chr12:27453931
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11+7106C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453931 | ||||||
| chr12:27454024
|
A | G | 224 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(221): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-11+7199A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454024 | ||||||
| chr12:27454173
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG01192.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-11+7348C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454173 | ||||||
| chr12:27454258
|
A | G | 199 | a0000c0010t0006g0238a0001c0001t0001g0002a0001c0001t0001g0012others(196): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.-11+7433A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454258 | ||||||
| chr12:27454332
|
G | A | 1 | a0002c0007t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11+7507G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454332 | ||||||
| chr12:27454389
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11+7564C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454389 | ||||||
| chr12:27454396
|
G | A | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+7571G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454396 | ||||||
| chr12:27454455
|
T | C | 210 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(207): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-11+7630T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454455 | ||||||
| chr12:27454517
|
T | C | 1 | a0003c0009t0004g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+7692T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454517 | ||||||
| chr12:27454548
|
C | T | 2 | a0002c0003t0003g0159a0002c0003t0003g0160 | 2 | NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-11+7723C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454548 | ||||||
| chr12:27454710
|
T | A | 199 | a0000c0010t0006g0238a0001c0001t0001g0002a0001c0001t0001g0012others(196): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.-11+7885T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454710 | ||||||
| chr12:27454743
|
G | A | 11 | a0001c0001t0002g0324a0001c0001t0002g0325a0001c0001t0002g0326others(8): Show | 12 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+7918G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454743 | ||||||
| chr12:27454910
|
C | CT | 203 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(200): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-11+8091dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27454910 | |||||
| chr12:27454998
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-11+8173C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454998 | ||||||
| chr12:27455190
|
A | G | 203 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(200): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-11+8365A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455190 | ||||||
| chr12:27455228
|
C | G | 1 | a0002c0003t0001g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11+8403C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455228 | ||||||
| chr12:27455339
|
A | G | 1 | a0001c0001t0002g0076 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-11+8514A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455339 | ||||||
| chr12:27455385
|
A | G | 2 | a0001c0001t0002g0324a0001c0001t0002g0325 | 2 | HG01255.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+8560A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455385 | ||||||
| chr12:27455487
|
A | C | 1 | a0001c0001t0001g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-11+8662A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455487 | ||||||
| chr12:27455624
|
A | G | 209 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(206): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-11+8799A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455624 | ||||||
| chr12:27455670
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11+8845T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455670 | ||||||
| chr12:27455691
|
G | A | 209 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(206): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-11+8866G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455691 | ||||||
| chr12:27455730
|
T | C | 1 | a0001c0001t0002g0007 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.-11+8905T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455730 | ||||||
| chr12:27455783
|
G | A | 29 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(26): Show | 32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+8958G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455783 | ||||||
| chr12:27455826
|
G | A | 29 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(26): Show | 32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+9001G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455826 | ||||||
| chr12:27455838
|
G | C | 1 | a0002c0007t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-11+9013G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455838 | ||||||
| chr12:27455976
|
G | A | 5 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(2): Show | 5 | NA18962.hp1 NA18978.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+9151G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455976 | ||||||
| chr12:27455978
|
G | A | 2 | a0000c0006t0005g0289a0000c0006t0005g0290 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-11+9153G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455978 | ||||||
| chr12:27456000
|
G | A | 1 | a0003c0002t0002g0095 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-11+9175G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456000 | ||||||
| chr12:27456063
|
G | A | 169 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(166): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-11+9238G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456063 | ||||||
| chr12:27456086
|
A | T | 3 | a0002c0019t0004g0295a0005c0014t0001g0320a0005c0014t0001g0321 | 3 | HG01884.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+9261A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456086 | ||||||
| chr12:27456107
|
C | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+9282C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456107 | ||||||
| chr12:27456140
|
G | A | 141 | a0000c0010t0006g0238a0001c0001t0001g0002a0001c0001t0001g0012others(138): Show | 147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-11+9315G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456140 | ||||||
| chr12:27456163
|
C | T | 25 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(22): Show | 28 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-11+9338C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456163 | ||||||
| chr12:27456185
|
A | G | 1 | a0002c0007t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11+9360A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456185 | ||||||
| chr12:27456202
|
T | G | 168 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(165): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-11+9377T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456202 | ||||||
| chr12:27456247
|
T | G | 168 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(165): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-11+9422T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456247 | ||||||
| chr12:27456323
|
T | G | 169 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(166): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-11+9498T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456323 | ||||||
| chr12:27456343
|
G | A | 11 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(8): Show | 13 | HG01192.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+9518G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456343 | ||||||
| chr12:27456365
|
G | A | 5 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00544.hp2 NA18975.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+9540G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456365 | ||||||
| chr12:27456384
|
T | G | 4 | a0000c0022t0006g0030a0002c0019t0004g0295a0005c0014t0001g0320others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+9559T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456384 | ||||||
| chr12:27456461
|
G | T | 1 | a0006c0013t0002g0330 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+9636G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456461 | ||||||
| chr12:27456476
|
G | A | 11 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(8): Show | 13 | HG01192.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+9651G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456476 | ||||||
| chr12:27456499
|
G | T | 1 | a0008c0018t0001g0267 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+9674G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456499 | ||||||
| chr12:27456513
|
G | C | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-11+9688G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456513 | ||||||
| chr12:27456525
|
C | A | 1 | a0000c0006t0006g0033 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-11+9700C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456525 | ||||||
| chr12:27456560
|
G | A | 1 | a0003c0002t0002g0053 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-11+9735G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456560 | ||||||
| chr12:27456578
|
C | G | 4 | a0000c0022t0006g0030a0002c0019t0004g0295a0005c0014t0001g0320others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+9753C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456578 | ||||||
| chr12:27456592
|
G | T | 10 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+9767G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456592 | ||||||
| chr12:27456737
|
T | C | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+9912T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456737 | ||||||
| chr12:27456943
|
C | T | 3 | a0002c0019t0004g0295a0005c0014t0001g0320a0005c0014t0001g0321 | 3 | HG01884.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+10118C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456943 | ||||||
| chr12:27457140
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0296 | 2 | HG01192.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-11+10315C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457140 | ||||||
| chr12:27457141
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11+10316G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457141 | ||||||
| chr12:27457164
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-11+10339G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457164 | ||||||
| chr12:27457265
|
G | A | 3 | a0002c0019t0004g0295a0005c0014t0001g0320a0005c0014t0001g0321 | 3 | HG01884.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+10440G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457265 | ||||||
| chr12:27457413
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-11+10588C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457413 | ||||||
| chr12:27457514
|
C | G | 41 | a0001c0001t0004g0270a0001c0004t0004g0269a0001c0004t0004g0278others(38): Show | 46 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.-11+10689C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457514 | ||||||
| chr12:27457571
|
C | T | 1 | a0001c0004t0001g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-11+10746C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457571 | ||||||
| chr12:27457637
|
A | G | 217 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(214): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-11+10812A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457637 | ||||||
| chr12:27457640
|
G | A | 43 | a0001c0001t0004g0270a0001c0004t0004g0269a0001c0004t0004g0278others(40): Show | 48 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.-11+10815G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457640 | ||||||
| chr12:27457855
|
T | G | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02451.hp2 HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+11030T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457855 | ||||||
| chr12:27457868
|
G | A | 25 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(22): Show | 28 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-11+11043G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457868 | ||||||
| chr12:27457869
|
G | T | 25 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(22): Show | 28 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-11+11044G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457869 | ||||||
| chr12:27457988
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-11+11163G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457988 | ||||||
| chr12:27458163
|
C | T | 140 | a0000c0010t0006g0238a0001c0001t0001g0002a0001c0001t0001g0012others(137): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-11+11338C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458163 | ||||||
| chr12:27458414
|
C | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG02451.hp2 HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+11589C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458414 | ||||||
| chr12:27458445
|
C | G | 29 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(26): Show | 32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+11620C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458445 | ||||||
| chr12:27458480
|
A | C | 142 | a0000c0010t0006g0238a0001c0001t0001g0002a0001c0001t0001g0012others(139): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-11+11655A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458480 | ||||||
| chr12:27458649
|
G | A | 2 | a0002c0005t0004g0311a0002c0005t0004g0312 | 2 | HG02257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-11+11824G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458649 | ||||||
| chr12:27458690
|
A | C | 1 | a0001c0001t0001g0262 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-11+11865A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458690 | ||||||
| chr12:27458773
|
G | A | 1 | a0002c0003t0003g0131 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-10-11849G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458773 | ||||||
| chr12:27458834
|
C | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0183 | 7 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-11788C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458834 | ||||||
| chr12:27458874
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-10-11748G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458874 | ||||||
| chr12:27458888
|
G | GA | 16 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(13): Show | 19 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10-11717dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27458888 | |||||
| chr12:27458972
|
T | G | 33 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(30): Show | 36 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-10-11650T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458972 | ||||||
| chr12:27459080
|
G | A | 1 | a0002c0003t0003g0133 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-10-11542G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459080 | ||||||
| chr12:27459112
|
G | A | 1 | a0001c0004t0001g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-10-11510G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459112 | ||||||
| chr12:27459131
|
G | C | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-11491G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459131 | ||||||
| chr12:27459135
|
C | T | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-11487C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459135 | ||||||
| chr12:27459174
|
A | G | 12 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0005t0001g0018others(9): Show | 12 | HG00741.hp2 HG02809.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-11448A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459174 | ||||||
| chr12:27459186
|
C | CA | 8 | a0001c0001t0002g0055a0001c0001t0002g0100a0003c0002t0002g0056others(5): Show | 8 | HG03239.hp1 HG03831.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-11414dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | |||||
| chr12:27459186
|
CA | C | 68 | a0001c0001t0001g0171a0001c0001t0001g0186a0001c0001t0001g0187others(65): Show | 74 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-10-11414delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | |||||
| chr12:27459186
|
CAA | C | 118 | a0000c0010t0006g0238a0001c0001t0001g0002a0001c0001t0001g0012others(115): Show | 124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-10-11415_-10-1141 others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | |||||
| chr12:27459186
|
CAAA | C | 21 | a0000c0010t0006g0333a0000c0010t0006g0334a0000c0010t0006g0335others(18): Show | 21 | HG01168.hp2 HG02015.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.-10-11416_-10-1141 others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | |||||
| chr12:27459186
|
CAAAAAA | C | 24 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(21): Show | 27 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-10-11419_-10-1141 others(10): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | |||||
| chr12:27459193
|
A | G | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-11429A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459193 | ||||||
| chr12:27459268
|
T | G | 1 | a0000c0010t0006g0333 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-10-11354T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459268 | ||||||
| chr12:27459272
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-10-11350T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459272 | ||||||
| chr12:27459311
|
T | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG01975.hp2 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-11311T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459311 | ||||||
| chr12:27459351
|
C | T | 4 | a0000c0022t0006g0030a0002c0019t0004g0295a0005c0014t0001g0320others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-11271C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459351 | ||||||
| chr12:27459384
|
T | C | 1 | a0001c0004t0002g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-10-11238T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459384 | ||||||
| chr12:27459550
|
T | A | 29 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(26): Show | 32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10-11072T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459550 | ||||||
| chr12:27459584
|
A | C | 46 | a0000c0017t0005g0020a0001c0001t0004g0270a0001c0004t0004g0269others(43): Show | 51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-11038A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459584 | ||||||
| chr12:27459610
|
G | A | 29 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(26): Show | 32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10-11012G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459610 | ||||||
| chr12:27460118
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-10-10504C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460118 | ||||||
| chr12:27460167
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-10-10455A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460167 | ||||||
| chr12:27460168
|
G | C | 20 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(17): Show | 23 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-10-10454G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460168 | ||||||
| chr12:27460290
|
C | T | 20 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(17): Show | 23 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-10-10332C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460290 | ||||||
| chr12:27460400
|
A | G | 1 | a0001c0004t0002g0322 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-10-10222A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460400 | ||||||
| chr12:27460413
|
G | A | 8 | a0001c0001t0002g0324a0001c0001t0002g0325a0002c0005t0003g0329others(5): Show | 9 | HG01255.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-10209G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460413 | ||||||
| chr12:27460429
|
A | T | 3 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0315 | 3 | HG02257.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10-10193A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460429 | ||||||
| chr12:27460556
|
G | GTGA | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0281others(3): Show | 8 | HG02109.hp1 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-10064_-10-1006 others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27460556 | |||||
| chr12:27460879
|
G | A | 1 | a0003c0002t0002g0057 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-10-9743G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460879 | ||||||
| chr12:27460921
|
C | T | 1 | a0003c0002t0002g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-10-9701C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460921 | ||||||
| chr12:27460937
|
G | A | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-10-9685G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460937 | ||||||
| chr12:27461138
|
A | G | 158 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(155): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-10-9484A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461138 | ||||||
| chr12:27461186
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-10-9436C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461186 | ||||||
| chr12:27461323
|
G | A | 46 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(43): Show | 51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-9299G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461323 | ||||||
| chr12:27461342
|
T | G | 8 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(5): Show | 8 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-9280T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461342 | ||||||
| chr12:27461407
|
G | A | 42 | a0001c0001t0004g0270a0001c0004t0004g0269a0002c0003t0003g0004others(39): Show | 47 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-10-9215G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461407 | ||||||
| chr12:27461415
|
C | A | 1 | a0006c0013t0002g0330 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-10-9207C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461415 | ||||||
| chr12:27461433
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0002g0250 | 2 | HG02738.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-10-9189C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461433 | ||||||
| chr12:27461534
|
G | A | 1 | a0003c0002t0002g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-10-9088G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461534 | ||||||
| chr12:27461607
|
C | T | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-9015C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461607 | ||||||
| chr12:27461616
|
T | C | 13 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(10): Show | 16 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-9006T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461616 | ||||||
| chr12:27461698
|
C | T | 66 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(63): Show | 74 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-8924C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461698 | ||||||
| chr12:27461808
|
C | A | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-8814C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461808 | ||||||
| chr12:27461827
|
A | G | 42 | a0001c0001t0004g0270a0001c0004t0004g0269a0002c0003t0003g0004others(39): Show | 47 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-10-8795A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461827 | ||||||
| chr12:27462020
|
G | T | 10 | a0002c0005t0004g0303a0002c0005t0004g0304a0002c0005t0004g0305others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-8602G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462020 | ||||||
| chr12:27462209
|
G | A | 1 | a0003c0009t0004g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-8413G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462209 | ||||||
| chr12:27462248
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10-8374T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462248 | ||||||
| chr12:27462339
|
CCTTT | C | 9 | a0001c0001t0001g0164a0001c0001t0001g0244a0001c0001t0001g0245others(6): Show | 9 | HG02040.hp2 HG02165.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-8278_-10-8275d others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27462339 | |||||
| chr12:27462402
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-10-8220G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462402 | ||||||
| chr12:27462441
|
A | G | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-8181A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462441 | ||||||
| chr12:27462473
|
G | T | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-8149G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462473 | ||||||
| chr12:27462510
|
G | A | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-8112G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462510 | ||||||
| chr12:27462532
|
A | T | 2 | a0001c0001t0002g0069a0001c0001t0002g0070 | 2 | HG00642.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-10-8090A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462532 | ||||||
| chr12:27462600
|
T | C | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-8022T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462600 | ||||||
| chr12:27462627
|
G | A | 1 | a0002c0005t0004g0311 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-10-7995G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462627 | ||||||
| chr12:27462675
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-10-7947C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462675 | ||||||
| chr12:27462736
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-10-7886A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462736 | ||||||
| chr12:27462738
|
T | C | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-7884T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462738 | ||||||
| chr12:27462876
|
C | G | 46 | a0000c0017t0005g0020a0001c0001t0004g0270a0001c0004t0004g0269others(43): Show | 51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-7746C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462876 | ||||||
| chr12:27462881
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-10-7741C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462881 | ||||||
| chr12:27463084
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-10-7538C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463084 | ||||||
| chr12:27463151
|
C | T | 4 | a0000c0022t0006g0030a0002c0019t0004g0295a0005c0014t0001g0320others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-7471C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463151 | ||||||
| chr12:27463248
|
C | A | 56 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(53): Show | 64 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-10-7374C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463248 | ||||||
| chr12:27463656
|
G | A | 4 | a0001c0001t0002g0324a0001c0001t0002g0325a0004c0011t0002g0017others(1): Show | 5 | HG01255.hp2 HG02486.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-6966G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463656 | ||||||
| chr12:27463695
|
T | C | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-6927T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463695 | ||||||
| chr12:27463815
|
G | A | 78 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(75): Show | 86 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.-10-6807G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463815 | ||||||
| chr12:27463844
|
A | C | 2 | a0003c0002t0002g0125a0003c0002t0002g0126 | 2 | NA18979.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-10-6778A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463844 | ||||||
| chr12:27463858
|
T | G | 1 | a0004c0011t0001g0274 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-10-6764T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463858 | ||||||
| chr12:27464021
|
C | T | 4 | a0000c0006t0006g0006a0000c0006t0006g0033a0005c0014t0001g0320others(1): Show | 5 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-6601C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464021 | ||||||
| chr12:27464066
|
C | T | 16 | a0001c0001t0002g0083a0002c0005t0003g0329a0002c0005t0004g0280others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-6556C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464066 | ||||||
| chr12:27464175
|
G | A | 41 | a0001c0001t0004g0270a0001c0004t0004g0269a0001c0004t0004g0278others(38): Show | 46 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.-10-6447G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464175 | ||||||
| chr12:27464311
|
C | T | 50 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0017t0005g0020others(47): Show | 57 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-10-6311C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464311 | ||||||
| chr12:27464414
|
G | A | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-6208G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464414 | ||||||
| chr12:27464512
|
C | T | 8 | a0003c0002t0002g0008a0003c0002t0002g0053a0003c0002t0002g0056others(5): Show | 9 | HG00733.hp2 HG01981.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-6110C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464512 | ||||||
| chr12:27464538
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-10-6084G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464538 | ||||||
| chr12:27464610
|
G | A | 2 | a0002c0003t0003g0135a0002c0019t0004g0295 | 2 | HG01884.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-10-6012G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464610 | ||||||
| chr12:27464650
|
G | A | 4 | a0000c0010t0006g0332a0000c0010t0006g0333a0000c0010t0006g0334others(1): Show | 4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-5972G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464650 | ||||||
| chr12:27464671
|
T | A | 1 | a0002c0016t0001g0315 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10-5951T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464671 | ||||||
| chr12:27464716
|
C | CA | 24 | a0000c0010t0006g0332a0000c0010t0006g0334a0001c0001t0001g0163others(21): Show | 25 | HG00609.hp1 HG00673.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-10-5883dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | |||||
| chr12:27464716
|
C | CAA | 5 | a0000c0006t0006g0006a0000c0006t0006g0033a0003c0002t0002g0103others(2): Show | 6 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5884_-10-5883d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | |||||
| chr12:27464716
|
C | CAAA | 8 | a0001c0001t0001g0184a0002c0005t0004g0304a0002c0005t0004g0305others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-5885_-10-5883d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | |||||
| chr12:27464716
|
C | CAAAA | 7 | a0002c0005t0003g0329a0002c0005t0004g0280a0002c0005t0004g0300others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-5886_-10-5883d others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | |||||
| chr12:27464716
|
C | CAAAAAAA others(6): Show |
2 | a0000c0017t0005g0020a0002c0021t0001g0019 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5895_-10-5883d others(15): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | |||||
| chr12:27464716
|
C | CAAAAAAA others(7): Show |
1 | a0002c0005t0001g0018 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-5896_-10-5883d others(16): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | |||||
| chr12:27464716
|
CA | C | 36 | a0000c0006t0005g0294a0001c0001t0001g0165a0001c0001t0001g0241others(33): Show | 40 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-10-5883delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | |||||
| chr12:27464717
|
A | G | 1 | a0001c0004t0001g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10-5905A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464717 | ||||||
| chr12:27464778
|
T | C | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5844T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464778 | ||||||
| chr12:27464787
|
C | T | 4 | a0000c0017t0005g0020a0001c0001t0002g0326a0002c0005t0001g0018others(1): Show | 4 | HG02976.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-5835C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464787 | ||||||
| chr12:27464788
|
G | A | 1 | a0001c0004t0001g0279 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-10-5834G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464788 | ||||||
| chr12:27464890
|
A | G | 169 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(166): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-10-5732A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464890 | ||||||
| chr12:27465001
|
C | T | 2 | a0001c0001t0002g0326a0001c0001t0002g0327 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-10-5621C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465001 | ||||||
| chr12:27465028
|
C | CA | 32 | a0000c0006t0005g0292a0000c0006t0006g0006a0000c0006t0006g0033others(29): Show | 34 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-10-5571dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465028 | |||||
| chr12:27465028
|
CA | C | 33 | a0000c0006t0005g0293a0001c0001t0001g0163a0001c0001t0001g0183others(30): Show | 34 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10-5571delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465028 | |||||
| chr12:27465028
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-5581_-10-5571d others(13): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465028 | |||||
| chr12:27465044
|
A | G | 3 | a0002c0003t0003g0140a0002c0003t0003g0156a0002c0003t0003g0157 | 3 | NA18959.hp2 NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-10-5578A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465044 | ||||||
| chr12:27465048
|
A | G | 43 | a0001c0001t0004g0270a0001c0004t0004g0269a0001c0004t0004g0278others(40): Show | 48 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.-10-5574A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465048 | ||||||
| chr12:27465052
|
G | A | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5570G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465052 | ||||||
| chr12:27465056
|
GA | G | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5562delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465056 | |||||
| chr12:27465066
|
GA | G | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5551delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465066 | |||||
| chr12:27465070
|
AAG | A | 2 | a0001c0001t0001g0016a0002c0003t0001g0288 | 3 | HG01192.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-10-5538_-10-5537d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465070 | |||||
| chr12:27465074
|
G | A | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5548G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465074 | ||||||
| chr12:27465076
|
G | A | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5546G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465076 | ||||||
| chr12:27465096
|
G | T | 2 | a0002c0003t0003g0150a0002c0003t0003g0151 | 2 | NA18939.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-10-5526G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465096 | ||||||
| chr12:27465105
|
C | G | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-5517C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465105 | ||||||
| chr12:27465379
|
C | T | 1 | a0003c0009t0003g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-5243C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465379 | ||||||
| chr12:27465401
|
G | A | 1 | a0002c0007t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-5221G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465401 | ||||||
| chr12:27465500
|
C | A | 2 | a0003c0002t0002g0104a0003c0002t0002g0127 | 2 | HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-10-5122C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465500 | ||||||
| chr12:27465541
|
G | A | 2 | a0001c0001t0001g0201a0001c0004t0001g0264 | 2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-10-5081G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465541 | ||||||
| chr12:27465864
|
C | T | 61 | a0000c0017t0005g0020a0000c0022t0006g0030a0001c0001t0004g0270others(58): Show | 66 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-10-4758C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465864 | ||||||
| chr12:27465998
|
A | G | 156 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-10-4624A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465998 | ||||||
| chr12:27466081
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-10-4541C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466081 | ||||||
| chr12:27466202
|
C | T | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-4420C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466202 | ||||||
| chr12:27466219
|
C | T | 1 | a0002c0007t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-4403C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466219 | ||||||
| chr12:27466332
|
A | C | 4 | a0003c0002t0002g0092a0003c0002t0002g0093a0003c0002t0002g0094others(1): Show | 4 | NA18959.hp1 NA18966.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-4290A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466332 | ||||||
| chr12:27466390
|
C | T | 42 | a0001c0001t0004g0270a0001c0004t0004g0269a0001c0004t0004g0278others(39): Show | 47 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-10-4232C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466390 | ||||||
| chr12:27466391
|
G | A | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-4231G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466391 | ||||||
| chr12:27466395
|
G | A | 31 | a0002c0003t0003g0004a0002c0003t0003g0005a0002c0003t0003g0011others(28): Show | 36 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.-10-4227G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466395 | ||||||
| chr12:27466612
|
G | C | 1 | a0002c0003t0003g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-10-4010G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466612 | ||||||
| chr12:27466791
|
A | G | 9 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(6): Show | 9 | HG01884.hp2 HG02015.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-3831A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466791 | ||||||
| chr12:27466894
|
A | G | 45 | a0000c0017t0005g0020a0001c0001t0004g0270a0001c0004t0004g0269others(42): Show | 50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-3728A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466894 | ||||||
| chr12:27467034
|
C | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-3588C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467034 | ||||||
| chr12:27467135
|
T | A | 2 | a0000c0010t0006g0333a0000c0010t0006g0335 | 2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-10-3487T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467135 | ||||||
| chr12:27467135
|
T | G | 68 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0334others(65): Show | 73 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10-3487T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467135 | ||||||
| chr12:27467277
|
A | T | 62 | a0000c0017t0005g0020a0000c0022t0006g0030a0001c0001t0004g0270others(59): Show | 67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-3345A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467277 | ||||||
| chr12:27467345
|
G | C | 3 | a0000c0017t0005g0020a0002c0005t0001g0018a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-3277G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467345 | ||||||
| chr12:27467407
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-10-3215A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467407 | ||||||
| chr12:27467657
|
G | A | 1 | a0002c0003t0001g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-2965G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467657 | ||||||
| chr12:27467691
|
A | G | 1 | a0002c0016t0001g0315 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10-2931A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467691 | ||||||
| chr12:27467699
|
T | C | 1 | a0003c0002t0002g0108 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-10-2923T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467699 | ||||||
| chr12:27467783
|
C | T | 245 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(242): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.-10-2839C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467783 | ||||||
| chr12:27467794
|
C | T | 70 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(67): Show | 75 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10-2828C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467794 | ||||||
| chr12:27468037
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10-2585T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468037 | ||||||
| chr12:27468053
|
A | C | 1 | a0003c0002t0002g0103 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-10-2569A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468053 | ||||||
| chr12:27468115
|
G | T | 1 | a0003c0002t0002g0095 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-10-2507G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468115 | ||||||
| chr12:27468143
|
C | T | 70 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(67): Show | 75 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10-2479C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468143 | ||||||
| chr12:27468154
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10-2468G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468154 | ||||||
| chr12:27468197
|
T | TA | 70 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(67): Show | 75 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10-2424dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27468197 | |||||
| chr12:27468208
|
T | G | 1 | a0002c0003t0003g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10-2414T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468208 | ||||||
| chr12:27468315
|
C | T | 8 | a0002c0003t0003g0005a0002c0003t0003g0084a0002c0003t0003g0145others(5): Show | 10 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-2307C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468315 | ||||||
| chr12:27468386
|
CAT | C | 62 | a0000c0017t0005g0020a0000c0022t0006g0030a0001c0001t0004g0270others(59): Show | 67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-2234_-10-2233d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27468386 | |||||
| chr12:27468409
|
G | T | 16 | a0000c0022t0006g0030a0002c0005t0003g0329a0002c0005t0004g0280others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-2213G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468409 | ||||||
| chr12:27468471
|
G | A | 1 | a0001c0004t0002g0322 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-10-2151G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468471 | ||||||
| chr12:27468627
|
T | C | 62 | a0000c0017t0005g0020a0000c0022t0006g0030a0001c0001t0004g0270others(59): Show | 67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-1995T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468627 | ||||||
| chr12:27468656
|
G | A | 62 | a0000c0017t0005g0020a0000c0022t0006g0030a0001c0001t0004g0270others(59): Show | 67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-1966G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468656 | ||||||
| chr12:27468677
|
G | T | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-10-1945G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468677 | ||||||
| chr12:27468684
|
G | A | 62 | a0000c0017t0005g0020a0000c0022t0006g0030a0001c0001t0004g0270others(59): Show | 67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-1938G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468684 | ||||||
| chr12:27468704
|
G | A | 1 | a0001c0001t0002g0007 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.-10-1918G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468704 | ||||||
| chr12:27468812
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-1810G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468812 | ||||||
| chr12:27468881
|
A | G | 1 | a0003c0002t0002g0123 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-10-1741A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468881 | ||||||
| chr12:27469009
|
C | T | 45 | a0000c0017t0005g0020a0001c0001t0004g0270a0001c0004t0004g0269others(42): Show | 50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-1613C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469009 | ||||||
| chr12:27469597
|
G | A | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-1025G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469597 | ||||||
| chr12:27469616
|
C | G | 45 | a0000c0017t0005g0020a0001c0001t0004g0270a0001c0004t0004g0269others(42): Show | 50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-1006C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469616 | ||||||
| chr12:27469648
|
A | G | 1 | a0002c0003t0003g0140 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-10-974A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469648 | ||||||
| chr12:27469652
|
G | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0281others(2): Show | 7 | HG02109.hp1 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-970G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469652 | ||||||
| chr12:27469660
|
G | T | 62 | a0000c0017t0005g0020a0000c0022t0006g0030a0001c0001t0004g0270others(59): Show | 67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-962G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469660 | ||||||
| chr12:27469724
|
A | G | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-898A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469724 | ||||||
| chr12:27469767
|
C | T | 1 | a0002c0003t0003g0133 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-10-855C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469767 | ||||||
| chr12:27469796
|
C | T | 42 | a0001c0001t0004g0270a0001c0004t0004g0269a0001c0004t0004g0278others(39): Show | 47 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-10-826C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469796 | ||||||
| chr12:27469858
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-10-764C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469858 | ||||||
| chr12:27469915
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-10-707A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469915 | ||||||
| chr12:27470038
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286 | 3 | HG02647.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-10-584G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470038 | ||||||
| chr12:27470180
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-10-442G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470180 | ||||||
| chr12:27470244
|
T | C | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-378T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470244 | ||||||
| chr12:27470301
|
C | A | 245 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(242): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.-10-321C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470301 | ||||||
| chr12:27470382
|
G | A | 72 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0010t0006g0238others(69): Show | 78 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10-240G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470382 | ||||||
| chr12:27470383
|
C | T | 72 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0010t0006g0238others(69): Show | 78 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10-239C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470383 | ||||||
| chr12:27470388
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10-234A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470388 | ||||||
| chr12:27470409
|
T | A | 2 | a0001c0001t0002g0085a0001c0004t0002g0322 | 2 | HG00673.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-10-213T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470409 | ||||||
| chr12:27470438
|
C | T | 1 | a0002c0007t0001g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-10-184C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470438 | ||||||
| chr12:27470500
|
G | GT | 241 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(238): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.-10-120dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27470500 | |||||
| chr12:27470557
|
A | G | 334 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(331): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-10-65A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470557 | ||||||
| chr12:27470795
|
T | C | 72 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0010t0006g0238others(69): Show | 78 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.134+30T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27470795 | ||||||
| chr12:27470818
|
G | A | 69 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0010t0006g0238others(66): Show | 75 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.134+53G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27470818 | ||||||
| chr12:27470883
|
A | C | 69 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0010t0006g0238others(66): Show | 75 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.134+118A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27470883 | ||||||
| chr12:27471124
|
C | T | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.134+359C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471124 | ||||||
| chr12:27471179
|
T | C | 1 | a0002c0003t0001g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.134+414T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471179 | ||||||
| chr12:27471261
|
T | C | 184 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(181): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.134+496T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471261 | ||||||
| chr12:27471302
|
G | A | 1 | a0003c0002t0002g0109 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.134+537G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471302 | ||||||
| chr12:27471431
|
C | T | 1 | a0003c0002t0002g0094 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.134+666C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471431 | ||||||
| chr12:27471539
|
C | T | 225 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0022t0006g0030others(222): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.134+774C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471539 | ||||||
| chr12:27471628
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134+863G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471628 | ||||||
| chr12:27471728
|
A | G | 45 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(42): Show | 50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.134+963A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471728 | ||||||
| chr12:27471952
|
G | A | 205 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(202): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.135-824G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471952 | ||||||
| chr12:27472009
|
T | C | 225 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(222): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.135-767T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472009 | ||||||
| chr12:27472104
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.135-672A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472104 | ||||||
| chr12:27472158
|
G | A | 45 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(42): Show | 50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.135-618G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472158 | ||||||
| chr12:27472248
|
G | A | 1 | a0001c0001t0002g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135-528G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472248 | ||||||
| chr12:27472366
|
C | G | 229 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(226): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.135-410C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472366 | ||||||
| chr12:27472367
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.135-409G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472367 | ||||||
| chr12:27472386
|
C | T | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.135-390C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472386 | ||||||
| chr12:27472490
|
C | T | 230 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(227): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.135-286C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472490 | ||||||
| chr12:27472491
|
A | G | 230 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(227): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.135-285A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472491 | ||||||
| chr12:27472526
|
T | C | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135-250T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472526 | ||||||
| chr12:27472529
|
G | C | 2 | a0000c0010t0006g0333a0000c0010t0006g0335 | 2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.135-247G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472529 | ||||||
| chr12:27472624
|
A | G | 4 | a0001c0001t0001g0231a0001c0001t0001g0266a0001c0001t0001g0287others(1): Show | 4 | HG00639.hp2 HG01192.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-152A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472624 | ||||||
| chr12:27472664
|
C | G | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-112C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472664 | ||||||
| chr12:27472724
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.135-52C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472724 | ||||||
| chr12:27472890
|
A | T | 230 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(227): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.234+15A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27472890 | ||||||
| chr12:27472945
|
C | T | 3 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.234+70C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27472945 | ||||||
| chr12:27472946
|
G | A | 230 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(227): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.234+71G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27472946 | ||||||
| chr12:27472954
|
T | C | 230 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(227): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.234+79T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27472954 | ||||||
| chr12:27473098
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.234+223C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473098 | ||||||
| chr12:27473245
|
G | A | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.234+370G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473245 | ||||||
| chr12:27473357
|
C | T | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234+482C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473357 | ||||||
| chr12:27473371
|
G | C | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+496G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473371 | ||||||
| chr12:27473458
|
C | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.234+583C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473458 | ||||||
| chr12:27473569
|
C | G | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+694C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473569 | ||||||
| chr12:27473678
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.234+803C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473678 | ||||||
| chr12:27473698
|
A | G | 58 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(55): Show | 64 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.234+823A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473698 | ||||||
| chr12:27473853
|
G | T | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.235-933G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473853 | ||||||
| chr12:27473933
|
A | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0230a0001c0001t0001g0271others(1): Show | 4 | HG00639.hp1 HG01175.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-853A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473933 | ||||||
| chr12:27473949
|
T | A | 157 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(154): Show | 173 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-837T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473949 | ||||||
| chr12:27473952
|
C | T | 1 | a0002c0005t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235-834C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473952 | ||||||
| chr12:27473956
|
G | T | 1 | a0002c0005t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235-830G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473956 | ||||||
| chr12:27474114
|
C | G | 155 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(152): Show | 170 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.235-672C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474114 | ||||||
| chr12:27474220
|
C | T | 1 | a0002c0003t0003g0151 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.235-566C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474220 | ||||||
| chr12:27474227
|
A | C | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.235-559A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474227 | ||||||
| chr12:27474536
|
G | A | 54 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(51): Show | 60 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.235-250G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474536 | ||||||
| chr12:27474567
|
G | A | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.235-219G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474567 | ||||||
| chr12:27474604
|
T | C | 157 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(154): Show | 173 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-182T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474604 | ||||||
| chr12:27474608
|
C | T | 7 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(4): Show | 7 | HG00642.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-178C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474608 | ||||||
| chr12:27474626
|
A | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(4): Show | 10 | HG01192.hp1 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.235-160A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474626 | ||||||
| chr12:27474634
|
T | C | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.235-152T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474634 | ||||||
| chr12:27474743
|
C | G | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.235-43C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474743 | ||||||
| chr12:27474914
|
G | A | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | splice_donor_variant&intron_variant | HIGH | c.362+1G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27474914 | ||||||
| chr12:27475101
|
G | A | 1 | a0001c0004t0001g0208 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.362+188G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475101 | ||||||
| chr12:27475172
|
G | A | 155 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(152): Show | 170 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.362+259G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475172 | ||||||
| chr12:27475195
|
T | C | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.362+282T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475195 | ||||||
| chr12:27475243
|
C | A | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.362+330C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475243 | ||||||
| chr12:27475260
|
T | G | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.363-322T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475260 | ||||||
| chr12:27475360
|
A | T | 4 | a0002c0003t0003g0153a0002c0003t0003g0154a0002c0003t0003g0155others(1): Show | 4 | HG03239.hp2 HG03688.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-222A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475360 | ||||||
| chr12:27475379
|
A | G | 1 | a0003c0009t0003g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.363-203A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475379 | ||||||
| chr12:27475399
|
C | T | 152 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(149): Show | 167 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.363-183C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475399 | ||||||
| chr12:27475809
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(130): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.512+78T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27475809 | ||||||
| chr12:27476250
|
A | T | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.512+519A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476250 | ||||||
| chr12:27476262
|
T | G | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+531T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476262 | ||||||
| chr12:27476471
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.512+740A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476471 | ||||||
| chr12:27476812
|
A | G | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+1081A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476812 | ||||||
| chr12:27476893
|
C | A | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1162C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476893 | ||||||
| chr12:27476970
|
T | C | 5 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(2): Show | 5 | HG00642.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+1239T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476970 | ||||||
| chr12:27476986
|
T | C | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1255T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476986 | ||||||
| chr12:27477000
|
T | A | 5 | a0003c0002t0002g0003a0003c0002t0002g0105a0003c0002t0002g0108others(2): Show | 7 | NA18977.hp2 NA18985.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.512+1269T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477000 | ||||||
| chr12:27477120
|
A | G | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1389A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477120 | ||||||
| chr12:27477167
|
G | T | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1436G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477167 | ||||||
| chr12:27477182
|
T | A | 1 | a0002c0005t0003g0329 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.512+1451T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477182 | ||||||
| chr12:27477209
|
GGTTTT | G | 11 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(8): Show | 12 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.512+1479_512+1483d others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | ||||||
| chr12:27477209
|
GGTTTTT | G | 44 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(41): Show | 49 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.512+1479_512+1484d others(8): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | ||||||
| chr12:27477209
|
GGTTTTTT | G | 3 | a0002c0003t0003g0140a0002c0003t0003g0158a0002c0015t0001g0313 | 3 | HG02257.hp1 NA18959.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.512+1479_512+1485d others(9): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | ||||||
| chr12:27477209
|
GGTTTTTT others(1): Show |
G | 3 | a0002c0007t0001g0028a0002c0007t0001g0031a0002c0007t0001g0032 | 3 | HG02055.hp2 HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.512+1479_512+1486d others(10): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | ||||||
| chr12:27477209
|
GGTTTTTT others(2): Show |
G | 10 | a0002c0005t0001g0027a0002c0007t0001g0021a0002c0007t0001g0022others(7): Show | 10 | HG00544.hp1 HG00741.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.512+1479_512+1487d others(11): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | ||||||
| chr12:27477209
|
GGTTTTTT others(3): Show |
G | 63 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(60): Show | 72 | HG00558.hp2 HG00733.hp2 HG01168.hp1 others(69): Show |
intron_variant | MODIFIER | c.512+1479_512+1488d others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | ||||||
| chr12:27477209
|
GGTTTTTT others(4): Show |
G | 1 | a0003c0002t0002g0125 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.512+1479_512+1489d others(13): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | ||||||
| chr12:27477209
|
GGTTTTTT others(6): Show |
G | 16 | a0002c0005t0001g0018a0002c0005t0003g0329a0002c0005t0004g0280others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.512+1479_512+1491d others(15): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | ||||||
| chr12:27477210
|
G | GT | 37 | a0001c0001t0001g0163a0001c0001t0001g0170a0001c0001t0001g0173others(34): Show | 37 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.512+1504dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | |||||
| chr12:27477210
|
G | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+1479G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477210 | ||||||
| chr12:27477210
|
GT | G | 31 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0180others(28): Show | 32 | HG00438.hp1 HG00544.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.512+1504delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | |||||
| chr12:27477210
|
GTT | G | 5 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0324others(2): Show | 6 | HG01255.hp2 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.512+1503_512+1504d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | |||||
| chr12:27477210
|
GTTTTTTT others(3): Show |
G | 1 | a0003c0002t0002g0113 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.512+1495_512+1504d others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | |||||
| chr12:27477210
|
GTTTTTTT others(6): Show |
G | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.512+1492_512+1504d others(15): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | |||||
| chr12:27477273
|
T | TTGCC | 8 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(5): Show | 8 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.512+1544_512+1547d others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477273 | |||||
| chr12:27477331
|
T | C | 1 | a0003c0002t0002g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.512+1600T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477331 | ||||||
| chr12:27477405
|
G | A | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+1674G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477405 | ||||||
| chr12:27477431
|
C | A | 1 | a0001c0004t0004g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.512+1700C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477431 | ||||||
| chr12:27477438
|
A | C | 58 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(55): Show | 64 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.512+1707A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477438 | ||||||
| chr12:27477496
|
G | T | 2 | a0003c0002t0002g0098a0003c0002t0002g0099 | 2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.512+1765G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477496 | ||||||
| chr12:27477576
|
A | AT | 310 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(307): Show | 335 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.512+1847dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477576 | |||||
| chr12:27477617
|
CTTCATTC others(3): Show |
C | 1 | a0001c0001t0002g0075 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.512+1899_512+1908d others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477617 | |||||
| chr12:27477634
|
C | CT | 26 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0001g0171others(23): Show | 27 | HG00280.hp2 HG00738.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.512+1919dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | |||||
| chr12:27477634
|
C | CTT | 86 | a0001c0001t0001g0179a0002c0005t0001g0018a0002c0005t0001g0027others(83): Show | 95 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.512+1918_512+1919d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | |||||
| chr12:27477634
|
C | CTTTTT | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.512+1915_512+1919d others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | |||||
| chr12:27477634
|
C | CTTTTTT | 41 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(38): Show | 46 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.512+1914_512+1919d others(8): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | |||||
| chr12:27477634
|
C | CTTTTTTT | 8 | a0000c0022t0006g0030a0002c0003t0001g0288a0002c0003t0003g0131others(5): Show | 8 | HG02080.hp1 HG03239.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.512+1913_512+1919d others(9): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | |||||
| chr12:27477634
|
C | CTTTTTTT others(3): Show |
1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+1910_512+1919d others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | |||||
| chr12:27477634
|
C | CTTTTTTT others(18): Show |
2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+1919_512+1920i others(27): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | |||||
| chr12:27477634
|
C | T | 3 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.512+1903C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477634 | ||||||
| chr12:27477722
|
TTA | T | 11 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(8): Show | 11 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.512+1993_512+1994d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477722 | |||||
| chr12:27477728
|
C | A | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1997C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477728 | ||||||
| chr12:27477775
|
A | G | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+2044A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477775 | ||||||
| chr12:27477804
|
T | A | 1 | a0001c0001t0001g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.512+2073T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477804 | ||||||
| chr12:27477868
|
T | A | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2137T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477868 | ||||||
| chr12:27477903
|
G | T | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2172G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477903 | ||||||
| chr12:27477943
|
C | T | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2212C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477943 | ||||||
| chr12:27477982
|
T | C | 9 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(6): Show | 9 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+2251T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477982 | ||||||
| chr12:27478058
|
G | C | 1 | a0002c0003t0001g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.512+2327G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478058 | ||||||
| chr12:27478103
|
A | G | 157 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(154): Show | 172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.512+2372A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478103 | ||||||
| chr12:27478153
|
C | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+2422C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478153 | ||||||
| chr12:27478162
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.512+2431A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478162 | ||||||
| chr12:27478183
|
G | A | 32 | a0002c0003t0003g0004a0002c0003t0003g0005a0002c0003t0003g0011others(29): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.512+2452G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478183 | ||||||
| chr12:27478195
|
T | C | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+2464T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478195 | ||||||
| chr12:27478269
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.512+2538A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478269 | ||||||
| chr12:27478368
|
T | C | 45 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(42): Show | 50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.512+2637T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478368 | ||||||
| chr12:27478447
|
A | C | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2716A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478447 | ||||||
| chr12:27478537
|
C | T | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2806C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478537 | ||||||
| chr12:27478615
|
C | T | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.512+2884C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478615 | ||||||
| chr12:27478651
|
C | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+2920C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478651 | ||||||
| chr12:27478736
|
A | G | 94 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+3005A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478736 | ||||||
| chr12:27478764
|
A | G | 157 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(154): Show | 172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.512+3033A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478764 | ||||||
| chr12:27478777
|
A | ACCAG | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3048_512+3049i others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27478777 | |||||
| chr12:27478780
|
C | A | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3049C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478780 | ||||||
| chr12:27478783
|
A | AC | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3052_512+3053i others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478783 | ||||||
| chr12:27478847
|
C | T | 2 | a0001c0004t0001g0215a0001c0004t0001g0240 | 2 | HG01106.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.512+3116C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478847 | ||||||
| chr12:27478907
|
T | C | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+3176T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478907 | ||||||
| chr12:27478912
|
G | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3181G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478912 | ||||||
| chr12:27479221
|
T | C | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.512+3490T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479221 | ||||||
| chr12:27479253
|
C | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3522C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479253 | ||||||
| chr12:27479255
|
T | G | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3524T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479255 | ||||||
| chr12:27479341
|
G | C | 2 | a0002c0003t0003g0159a0002c0003t0003g0160 | 2 | NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.512+3610G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479341 | ||||||
| chr12:27479347
|
C | T | 16 | a0002c0005t0001g0018a0002c0005t0003g0329a0002c0005t0004g0280others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.512+3616C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479347 | ||||||
| chr12:27479349
|
G | A | 16 | a0002c0005t0001g0018a0002c0005t0003g0329a0002c0005t0004g0280others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.512+3618G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479349 | ||||||
| chr12:27479402
|
G | T | 1 | a0006c0013t0001g0323 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.512+3671G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479402 | ||||||
| chr12:27479466
|
G | C | 1 | a0000c0006t0005g0294 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.512+3735G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479466 | ||||||
| chr12:27479482
|
T | C | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3751T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479482 | ||||||
| chr12:27479508
|
G | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3777G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479508 | ||||||
| chr12:27479544
|
TATG | T | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.512+3818_512+3820d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27479544 | |||||
| chr12:27479557
|
T | C | 9 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(6): Show | 9 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+3826T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479557 | ||||||
| chr12:27479619
|
G | A | 1 | a0003c0009t0004g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512+3888G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479619 | ||||||
| chr12:27479646
|
G | T | 71 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(68): Show | 80 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.512+3915G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479646 | ||||||
| chr12:27479651
|
C | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3920C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479651 | ||||||
| chr12:27479666
|
G | A | 2 | a0004c0011t0002g0017a0004c0011t0002g0328 | 3 | HG02486.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.512+3935G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479666 | ||||||
| chr12:27479695
|
A | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3964A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479695 | ||||||
| chr12:27479719
|
G | A | 87 | a0002c0005t0001g0018a0002c0005t0001g0027a0002c0005t0002g0120others(84): Show | 96 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.512+3988G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479719 | ||||||
| chr12:27479753
|
C | T | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+4022C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479753 | ||||||
| chr12:27479777
|
A | G | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4046A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479777 | ||||||
| chr12:27479866
|
A | T | 9 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(6): Show | 9 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+4135A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479866 | ||||||
| chr12:27479884
|
C | CAT | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4154_512+4155i others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27479884 | |||||
| chr12:27479886
|
C | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4155C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479886 | ||||||
| chr12:27479887
|
G | A | 2 | a0001c0001t0001g0016a0004c0011t0002g0017 | 4 | HG01192.hp1 HG02717.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.512+4156G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479887 | ||||||
| chr12:27479909
|
T | C | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4178T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479909 | ||||||
| chr12:27479941
|
C | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4210C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479941 | ||||||
| chr12:27480027
|
A | C | 2 | a0002c0003t0004g0268a0003c0009t0004g0172 | 2 | NA20752.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.512+4296A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480027 | ||||||
| chr12:27480119
|
A | T | 1 | a0001c0001t0001g0297 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.512+4388A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480119 | ||||||
| chr12:27480324
|
T | C | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4593T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480324 | ||||||
| chr12:27480357
|
T | A | 11 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(8): Show | 11 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.512+4626T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480357 | ||||||
| chr12:27480379
|
G | T | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.512+4648G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480379 | ||||||
| chr12:27480424
|
C | T | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4693C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480424 | ||||||
| chr12:27480448
|
C | A | 1 | a0001c0001t0002g0039 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.512+4717C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480448 | ||||||
| chr12:27480462
|
G | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG00738.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.512+4731G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480462 | ||||||
| chr12:27480707
|
C | G | 6 | a0001c0004t0001g0162a0001c0004t0001g0189a0001c0004t0001g0214others(3): Show | 6 | HG00099.hp1 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.512+4976C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480707 | ||||||
| chr12:27480708
|
C | T | 159 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(156): Show | 175 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.512+4977C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480708 | ||||||
| chr12:27480709
|
CT | C | 7 | a0001c0001t0001g0241a0001c0001t0001g0284a0001c0001t0001g0285others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.512+4979delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480709 | ||||||
| chr12:27480930
|
T | C | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5199T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480930 | ||||||
| chr12:27481092
|
G | C | 1 | a0003c0009t0001g0253 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.512+5361G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481092 | ||||||
| chr12:27481173
|
T | C | 3 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.512+5442T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481173 | ||||||
| chr12:27481277
|
A | G | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5546A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481277 | ||||||
| chr12:27481310
|
G | A | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5579G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481310 | ||||||
| chr12:27481325
|
G | A | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5594G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481325 | ||||||
| chr12:27481348
|
C | T | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5617C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481348 | ||||||
| chr12:27481449
|
A | G | 60 | a0003c0002t0001g0249a0003c0002t0002g0001a0003c0002t0002g0003others(57): Show | 69 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.512+5718A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481449 | ||||||
| chr12:27481462
|
A | G | 3 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.512+5731A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481462 | ||||||
| chr12:27481471
|
T | C | 72 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(69): Show | 81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.512+5740T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481471 | ||||||
| chr12:27481674
|
C | A | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.512+5943C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481674 | ||||||
| chr12:27481794
|
G | A | 2 | a0001c0001t0002g0326a0001c0001t0002g0327 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.512+6063G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481794 | ||||||
| chr12:27481810
|
A | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+6079A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481810 | ||||||
| chr12:27481841
|
T | C | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+6110T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481841 | ||||||
| chr12:27481871
|
T | G | 2 | a0005c0014t0001g0320a0005c0014t0001g0321 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+6140T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481871 | ||||||
| chr12:27482009
|
C | CTT | 96 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(93): Show | 105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+6288_512+6289d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27482009 | |||||
| chr12:27482093
|
A | G | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+6362A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482093 | ||||||
| chr12:27482171
|
T | A | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-6289T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482171 | ||||||
| chr12:27482267
|
T | C | 9 | a0002c0003t0003g0004a0002c0003t0003g0130a0002c0003t0003g0133others(6): Show | 11 | NA18940.hp2 NA18945.hp2 NA18961.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-6193T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482267 | ||||||
| chr12:27482283
|
C | A | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-6177C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482283 | ||||||
| chr12:27482341
|
G | T | 1 | a0003c0009t0004g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.513-6119G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482341 | ||||||
| chr12:27482551
|
T | C | 1 | a0001c0004t0001g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.513-5909T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482551 | ||||||
| chr12:27482662
|
G | A | 4 | a0001c0001t0001g0170a0001c0001t0001g0230a0001c0001t0001g0271others(1): Show | 4 | HG00639.hp1 HG01175.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-5798G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482662 | ||||||
| chr12:27482831
|
A | G | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-5629A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482831 | ||||||
| chr12:27482846
|
T | C | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-5614T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482846 | ||||||
| chr12:27482848
|
T | G | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-5612T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482848 | ||||||
| chr12:27482909
|
T | C | 1 | a0001c0001t0002g0250 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.513-5551T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482909 | ||||||
| chr12:27483068
|
A | T | 10 | a0002c0005t0001g0027a0002c0007t0001g0021a0002c0007t0001g0022others(7): Show | 10 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-5392A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483068 | ||||||
| chr12:27483200
|
G | A | 10 | a0002c0005t0001g0027a0002c0007t0001g0021a0002c0007t0001g0022others(7): Show | 10 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-5260G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483200 | ||||||
| chr12:27483242
|
A | C | 92 | a0000c0017t0005g0020a0000c0017t0005g0024a0000c0022t0006g0030others(89): Show | 101 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.513-5218A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483242 | ||||||
| chr12:27483378
|
C | T | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-5082C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483378 | ||||||
| chr12:27483385
|
C | G | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.513-5075C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483385 | ||||||
| chr12:27483497
|
A | T | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513-4963A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483497 | ||||||
| chr12:27483574
|
A | T | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-4886A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483574 | ||||||
| chr12:27483704
|
C | T | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513-4756C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483704 | ||||||
| chr12:27483705
|
G | A | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-4755G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483705 | ||||||
| chr12:27483803
|
A | C | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-4657A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483803 | ||||||
| chr12:27483901
|
A | G | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-4559A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483901 | ||||||
| chr12:27484007
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513-4453C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484007 | ||||||
| chr12:27484011
|
TTTACTA | T | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-4444_513-4439d others(8): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484011 | |||||
| chr12:27484195
|
A | G | 91 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0005t0001g0018others(88): Show | 100 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.513-4265A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484195 | ||||||
| chr12:27484216
|
C | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0273 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.513-4244C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484216 | ||||||
| chr12:27484236
|
C | G | 1 | a0001c0001t0002g0043 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.513-4224C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484236 | ||||||
| chr12:27484275
|
A | T | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-4185A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484275 | ||||||
| chr12:27484328
|
A | G | 157 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(154): Show | 172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.513-4132A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484328 | ||||||
| chr12:27484783
|
G | T | 2 | a0002c0003t0003g0150a0002c0003t0003g0151 | 2 | NA18939.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.513-3677G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484783 | ||||||
| chr12:27484809
|
T | C | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3651T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484809 | ||||||
| chr12:27484831
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3629G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484831 | ||||||
| chr12:27484839
|
A | G | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-3621A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484839 | ||||||
| chr12:27484847
|
A | G | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3613A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484847 | ||||||
| chr12:27484851
|
CA | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(84): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.513-3588delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484851 | |||||
| chr12:27484851
|
CAA | C | 15 | a0001c0001t0001g0013a0001c0001t0001g0179a0001c0001t0001g0226others(12): Show | 16 | HG01175.hp1 HG01361.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.513-3589_513-3588d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484851 | |||||
| chr12:27484851
|
CAAA | C | 16 | a0001c0001t0001g0284a0001c0001t0001g0286a0001c0001t0001g0319others(13): Show | 17 | HG00280.hp1 HG01069.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.513-3590_513-3588d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484851 | |||||
| chr12:27484862
|
AAAAAAAA others(10): Show |
A | 71 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(68): Show | 80 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.513-3596_513-3580d others(19): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484862 | |||||
| chr12:27484863
|
AAAAAAAA others(7): Show |
A | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-3595_513-3582d others(16): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484863 | |||||
| chr12:27484863
|
AAAAAAAA others(9): Show |
A | 23 | a0000c0017t0005g0020a0000c0017t0005g0024a0000c0022t0006g0030others(20): Show | 23 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.513-3595_513-3580d others(18): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484863 | |||||
| chr12:27484869
|
A | T | 2 | a0001c0001t0001g0260a0001c0008t0002g0046 | 2 | HG01069.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.513-3591A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484869 | ||||||
| chr12:27484870
|
AAAT | A | 13 | a0001c0001t0002g0007a0001c0001t0002g0054a0001c0001t0002g0055others(10): Show | 14 | HG00544.hp2 HG02015.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.513-3588_513-3586d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484870 | |||||
| chr12:27484871
|
A | AT | 10 | a0001c0001t0001g0265a0001c0004t0001g0162a0001c0004t0001g0189others(7): Show | 10 | HG00099.hp1 HG00673.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-3589_513-3588i others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484871 | ||||||
| chr12:27484871
|
A | T | 35 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0173others(32): Show | 37 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.513-3589A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484871 | ||||||
| chr12:27484871
|
AAT | A | 42 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0290others(39): Show | 48 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.513-3567_513-3566d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484871 | |||||
| chr12:27484872
|
AT | A | 10 | a0001c0001t0001g0164a0001c0001t0002g0072a0001c0001t0002g0073others(7): Show | 10 | HG00673.hp1 HG01258.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-3587delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484872 | ||||||
| chr12:27484872
|
ATAT | A | 10 | a0000c0006t0005g0167a0000c0006t0005g0293a0002c0003t0001g0197others(7): Show | 10 | HG00438.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-3587_513-3585d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484872 | ||||||
| chr12:27484873
|
T | A | 1 | a0001c0004t0001g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513-3587T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484873 | ||||||
| chr12:27484875
|
T | A | 37 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0290others(34): Show | 42 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.513-3585T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484875 | ||||||
| chr12:27484877
|
T | A | 3 | a0002c0003t0003g0131a0002c0003t0003g0143a0002c0003t0003g0145 | 3 | HG02004.hp1 HG02080.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.513-3583T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484877 | ||||||
| chr12:27484880
|
A | G | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-3580A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484880 | ||||||
| chr12:27484882
|
A | G | 94 | a0000c0017t0005g0020a0000c0017t0005g0024a0000c0022t0006g0030others(91): Show | 103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.513-3578A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484882 | ||||||
| chr12:27484888
|
A | G | 1 | a0002c0003t0001g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.513-3572A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484888 | ||||||
| chr12:27484921
|
C | A | 1 | a0001c0001t0001g0263 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.513-3539C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484921 | ||||||
| chr12:27484935
|
T | C | 1 | a0002c0007t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.513-3525T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484935 | ||||||
| chr12:27484949
|
T | G | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3511T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484949 | ||||||
| chr12:27484959
|
G | C | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3501G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484959 | ||||||
| chr12:27485074
|
T | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3386T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485074 | ||||||
| chr12:27485131
|
T | C | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3329T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485131 | ||||||
| chr12:27485141
|
T | TCTAA | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3317_513-3316i others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27485141 | |||||
| chr12:27485310
|
T | C | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3150T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485310 | ||||||
| chr12:27485323
|
C | T | 5 | a0002c0003t0003g0140a0002c0003t0003g0150a0002c0003t0003g0151others(2): Show | 5 | NA18939.hp1 NA18959.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.513-3137C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485323 | ||||||
| chr12:27485450
|
G | GCT | 17 | a0002c0005t0001g0018a0002c0005t0003g0329a0002c0005t0004g0280others(14): Show | 17 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.513-3010_513-3009i others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485450 | ||||||
| chr12:27485450
|
G | GT | 16 | a0000c0022t0006g0030a0001c0001t0001g0016a0001c0001t0001g0186others(13): Show | 17 | HG00609.hp1 HG00738.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.513-2993dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27485450 | |||||
| chr12:27485450
|
G | GTT | 8 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(5): Show | 8 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-2994_513-2993d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27485450 | |||||
| chr12:27485450
|
GT | G | 65 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(62): Show | 72 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.513-2993delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27485450 | |||||
| chr12:27485511
|
G | A | 1 | a0001c0004t0002g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.513-2949G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485511 | ||||||
| chr12:27485555
|
T | C | 1 | a0002c0003t0001g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.513-2905T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485555 | ||||||
| chr12:27485604
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.513-2856T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485604 | ||||||
| chr12:27485606
|
A | G | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-2854A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485606 | ||||||
| chr12:27485607
|
T | C | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-2853T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485607 | ||||||
| chr12:27485617
|
T | A | 1 | a0001c0004t0001g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.513-2843T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485617 | ||||||
| chr12:27485895
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-2565G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485895 | ||||||
| chr12:27485971
|
C | T | 1 | a0001c0001t0002g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.513-2489C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485971 | ||||||
| chr12:27485974
|
C | T | 1 | a0001c0001t0002g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.513-2486C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485974 | ||||||
| chr12:27486051
|
T | C | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-2409T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486051 | ||||||
| chr12:27486096
|
T | C | 11 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(8): Show | 11 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-2364T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486096 | ||||||
| chr12:27486131
|
T | C | 1 | a0001c0004t0001g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.513-2329T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486131 | ||||||
| chr12:27486162
|
C | A | 1 | a0001c0008t0002g0046 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.513-2298C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486162 | ||||||
| chr12:27486388
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.513-2072C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486388 | ||||||
| chr12:27486448
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.513-2012C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486448 | ||||||
| chr12:27486619
|
G | T | 3 | a0003c0002t0002g0059a0003c0002t0002g0060a0003c0002t0002g0078 | 3 | HG02071.hp2 HG02074.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.513-1841G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486619 | ||||||
| chr12:27486671
|
T | G | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-1789T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486671 | ||||||
| chr12:27486693
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.513-1767A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486693 | ||||||
| chr12:27486758
|
G | A | 1 | a0003c0002t0002g0129 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.513-1702G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486758 | ||||||
| chr12:27486816
|
C | T | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-1644C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486816 | ||||||
| chr12:27486825
|
A | G | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-1635A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486825 | ||||||
| chr12:27486959
|
A | C | 2 | a0001c0001t0002g0326a0001c0001t0002g0327 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.513-1501A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486959 | ||||||
| chr12:27486971
|
G | T | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-1489G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486971 | ||||||
| chr12:27487087
|
C | T | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513-1373C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487087 | ||||||
| chr12:27487123
|
C | A | 1 | a0003c0002t0002g0108 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.513-1337C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487123 | ||||||
| chr12:27487144
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513-1316T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487144 | ||||||
| chr12:27487246
|
C | T | 1 | a0003c0002t0002g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.513-1214C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487246 | ||||||
| chr12:27487343
|
C | CT | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-1110dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487343 | |||||
| chr12:27487352
|
A | C | 3 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.513-1108A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487352 | ||||||
| chr12:27487388
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.513-1072C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487388 | ||||||
| chr12:27487418
|
T | C | 1 | a0003c0009t0003g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.513-1042T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487418 | ||||||
| chr12:27487424
|
GTAGTCTT others(9): Show |
G | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.513-1035_513-1020d others(18): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487424 | ||||||
| chr12:27487440
|
T | G | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-1020T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487440 | ||||||
| chr12:27487535
|
C | T | 4 | a0001c0001t0001g0283a0002c0005t0001g0018a0002c0005t0004g0303others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.513-925C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487535 | ||||||
| chr12:27487537
|
C | T | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-923C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487537 | ||||||
| chr12:27487538
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-922G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487538 | ||||||
| chr12:27487629
|
G | A | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-831G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487629 | ||||||
| chr12:27487635
|
G | A | 2 | a0002c0003t0001g0197a0002c0003t0001g0204 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.513-825G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487635 | ||||||
| chr12:27487698
|
G | A | 2 | a0001c0001t0002g0058a0001c0004t0001g0240 | 2 | HG03041.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.513-762G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487698 | ||||||
| chr12:27487699
|
C | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-761C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487699 | ||||||
| chr12:27487753
|
C | CT | 8 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(5): Show | 8 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-691dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487753 | |||||
| chr12:27487753
|
C | CTT | 16 | a0002c0005t0001g0018a0002c0005t0003g0329a0002c0005t0004g0280others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.513-692_513-691dup others(2): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487753 | |||||
| chr12:27487753
|
CT | C | 62 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(59): Show | 68 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.513-691delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487753 | |||||
| chr12:27487772
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.513-688C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487772 | ||||||
| chr12:27487877
|
T | G | 1 | a0001c0001t0001g0218 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.513-583T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487877 | ||||||
| chr12:27487941
|
T | A | 1 | a0003c0002t0002g0115 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.513-519T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487941 | ||||||
| chr12:27487941
|
T | TA | 97 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(94): Show | 106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-517dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487941 | |||||
| chr12:27488001
|
G | A | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-459G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488001 | ||||||
| chr12:27488017
|
T | G | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-443T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488017 | ||||||
| chr12:27488061
|
T | C | 1 | a0000c0022t0006g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513-399T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488061 | ||||||
| chr12:27488133
|
T | A | 1 | a0001c0001t0002g0122 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.513-327T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488133 | ||||||
| chr12:27488155
|
C | T | 3 | a0003c0002t0004g0195a0003c0002t0004g0202a0003c0002t0004g0203 | 3 | HG02602.hp2 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.513-305C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488155 | ||||||
| chr12:27488278
|
T | C | 3 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.513-182T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488278 | ||||||
| chr12:27488413
|
G | A | 1 | a0002c0005t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.513-47G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488413 | ||||||
| chr12:27488442
|
A | G | 90 | a0002c0005t0001g0018a0002c0005t0001g0027a0002c0005t0002g0120others(87): Show | 99 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.513-18A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488442 | ||||||
| chr12:27488641
|
G | A | 2 | a0002c0003t0004g0268a0003c0009t0004g0172 | 2 | NA20752.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.600+94G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488641 | ||||||
| chr12:27488753
|
A | G | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+206A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488753 | ||||||
| chr12:27488769
|
C | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+222C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488769 | ||||||
| chr12:27488784
|
T | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+237T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488784 | ||||||
| chr12:27488801
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+254G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488801 | ||||||
| chr12:27488819
|
G | C | 1 | a0008c0018t0001g0267 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.600+272G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488819 | ||||||
| chr12:27488851
|
C | T | 72 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(69): Show | 81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+304C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488851 | ||||||
| chr12:27488895
|
G | C | 1 | a0003c0002t0002g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.600+348G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488895 | ||||||
| chr12:27488957
|
T | G | 44 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(41): Show | 49 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.600+410T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488957 | ||||||
| chr12:27489024
|
T | C | 3 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.600+477T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489024 | ||||||
| chr12:27489142
|
G | A | 1 | a0001c0001t0002g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600+595G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489142 | ||||||
| chr12:27489145
|
T | A | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+598T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489145 | ||||||
| chr12:27489190
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+643G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489190 | ||||||
| chr12:27489296
|
A | G | 157 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(154): Show | 172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.600+749A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489296 | ||||||
| chr12:27489302
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.600+755G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489302 | ||||||
| chr12:27489339
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+792G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489339 | ||||||
| chr12:27489461
|
A | G | 72 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(69): Show | 81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+914A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489461 | ||||||
| chr12:27489602
|
G | A | 6 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(3): Show | 6 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+1055G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489602 | ||||||
| chr12:27489605
|
A | G | 3 | a0000c0017t0005g0020a0000c0017t0005g0024a0002c0021t0001g0019 | 3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.600+1058A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489605 | ||||||
| chr12:27489609
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1062G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489609 | ||||||
| chr12:27490078
|
C | A | 2 | a0003c0002t0002g0106a0003c0002t0002g0116 | 2 | HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.600+1531C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490078 | ||||||
| chr12:27490149
|
C | T | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1602C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490149 | ||||||
| chr12:27490250
|
G | A | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.600+1703G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490250 | ||||||
| chr12:27490269
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1722G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490269 | ||||||
| chr12:27490306
|
C | T | 71 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(68): Show | 80 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.600+1759C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490306 | ||||||
| chr12:27490506
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1959G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490506 | ||||||
| chr12:27490514
|
A | G | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1967A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490514 | ||||||
| chr12:27490673
|
T | G | 1 | a0003c0002t0002g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.600+2126T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490673 | ||||||
| chr12:27490678
|
C | T | 2 | a0003c0002t0002g0103a0003c0002t0002g0128 | 2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.600+2131C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490678 | ||||||
| chr12:27490718
|
T | C | 157 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(154): Show | 172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.600+2171T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490718 | ||||||
| chr12:27490720
|
C | T | 4 | a0002c0015t0001g0313a0002c0015t0001g0314a0002c0016t0001g0239others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+2173C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490720 | ||||||
| chr12:27490741
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+2194G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490741 | ||||||
| chr12:27490852
|
C | A | 1 | a0001c0004t0002g0322 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.600+2305C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490852 | ||||||
| chr12:27491094
|
G | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+2547G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491094 | ||||||
| chr12:27491162
|
C | T | 1 | a0003c0002t0002g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.600+2615C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491162 | ||||||
| chr12:27491261
|
G | T | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+2714G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491261 | ||||||
| chr12:27491353
|
ATAG | A | 99 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(96): Show | 108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+2807_600+2809d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491353 | ||||||
| chr12:27491426
|
G | A | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-2874G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491426 | ||||||
| chr12:27491562
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.601-2738C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491562 | ||||||
| chr12:27491573
|
C | G | 1 | a0001c0004t0001g0212 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.601-2727C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491573 | ||||||
| chr12:27491705
|
T | G | 54 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(51): Show | 60 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.601-2595T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491705 | ||||||
| chr12:27491710
|
C | CT | 47 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(44): Show | 53 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.601-2577dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 27491710 | |||||
| chr12:27491710
|
C | CTT | 11 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(8): Show | 11 | HG00642.hp2 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.601-2578_601-2577d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 27491710 | |||||
| chr12:27491947
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0062 | 2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.601-2353C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491947 | ||||||
| chr12:27491978
|
G | T | 18 | a0002c0005t0001g0018a0002c0005t0003g0329a0002c0005t0004g0280others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.601-2322G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491978 | ||||||
| chr12:27492068
|
T | C | 72 | a0002c0005t0001g0027a0002c0005t0002g0120a0002c0007t0001g0021others(69): Show | 81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.601-2232T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492068 | ||||||
| chr12:27492099
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.601-2201G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492099 | ||||||
| chr12:27492139
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.601-2161A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492139 | ||||||
| chr12:27492149
|
T | G | 45 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0233others(42): Show | 50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.601-2151T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492149 | ||||||
| chr12:27492209
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-2091A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492209 | ||||||
| chr12:27492258
|
T | C | 2 | a0002c0007t0001g0025a0002c0007t0001g0028 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.601-2042T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492258 | ||||||
| chr12:27492276
|
G | C | 1 | a0001c0001t0001g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.601-2024G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492276 | ||||||
| chr12:27492311
|
T | G | 18 | a0002c0005t0001g0018a0002c0005t0003g0329a0002c0005t0004g0280others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.601-1989T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492311 | ||||||
| chr12:27492456
|
G | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.601-1844G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492456 | ||||||
| chr12:27492743
|
A | G | 9 | a0002c0005t0001g0018a0002c0005t0004g0303a0002c0005t0004g0304others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-1557A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492743 | ||||||
| chr12:27492780
|
C | A | 3 | a0001c0004t0001g0162a0001c0004t0001g0189a0001c0004t0001g0214 | 3 | HG00099.hp1 HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.601-1520C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492780 | ||||||
| chr12:27492945
|
A | G | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.601-1355A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492945 | ||||||
| chr12:27493014
|
G | A | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-1286G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493014 | ||||||
| chr12:27493035
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.601-1265A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493035 | ||||||
| chr12:27493116
|
G | A | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-1184G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493116 | ||||||
| chr12:27493132
|
G | T | 54 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(51): Show | 61 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.601-1168G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493132 | ||||||
| chr12:27493187
|
G | A | 5 | a0000c0010t0006g0238a0000c0010t0006g0332a0000c0010t0006g0333others(2): Show | 5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-1113G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493187 | ||||||
| chr12:27493251
|
T | C | 1 | a0001c0004t0001g0191 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.601-1049T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493251 | ||||||
| chr12:27493282
|
A | G | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.601-1018A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493282 | ||||||
| chr12:27493298
|
G | A | 76 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(73): Show | 82 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.601-1002G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493298 | ||||||
| chr12:27493339
|
A | T | 9 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(6): Show | 10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-961A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493339 | ||||||
| chr12:27493417
|
A | G | 2 | a0006c0013t0001g0323a0006c0013t0002g0330 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.601-883A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493417 | ||||||
| chr12:27493532
|
CA | C | 60 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0010t0006g0238others(57): Show | 66 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.601-756delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 27493532 | |||||
| chr12:27493548
|
A | T | 52 | a0000c0006t0006g0006a0000c0006t0006g0033a0000c0010t0006g0238others(49): Show | 58 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.601-752A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493548 | ||||||
| chr12:27493604
|
T | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG01975.hp2 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-696T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493604 | ||||||
| chr12:27493697
|
G | C | 2 | a0006c0013t0001g0323a0006c0013t0002g0330 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.601-603G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493697 | ||||||
| chr12:27493793
|
C | T | 133 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(130): Show | 150 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.601-507C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493793 | ||||||
| chr12:27493971
|
T | G | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.601-329T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493971 | ||||||
| chr12:27493996
|
T | A | 2 | a0000c0006t0006g0006a0000c0006t0006g0033 | 3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.601-304T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493996 | ||||||
| chr12:27494076
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.601-224A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27494076 | ||||||
| chr12:27494261
|
T | C | 1 | a0002c0005t0004g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601-39T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27494261 | ||||||
| chr12:27494276
|
C | A | 5 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(2): Show | 5 | HG02572.hp2 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-24C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27494276 | ||||||
| chr12:27494449
|
C | T | 19 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(16): Show | 21 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.657+93C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27494449 | ||||||
| chr12:27494487
|
T | TTTA | 28 | a0000c0022t0006g0030a0001c0001t0001g0016a0001c0001t0001g0205others(25): Show | 29 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.657+166_657+168dup others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | |||||
| chr12:27494487
|
T | TTTATTA | 70 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0163others(67): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.657+163_657+168dup others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | |||||
| chr12:27494487
|
T | TTTATTAT others(2): Show |
51 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0086others(48): Show | 53 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.657+160_657+168dup others(9): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | |||||
| chr12:27494487
|
T | TTTATTAT others(5): Show |
1 | a0001c0004t0001g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.657+157_657+168dup others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | |||||
| chr12:27494487
|
TTTA | T | 20 | a0000c0017t0005g0020a0000c0017t0005g0024a0001c0001t0001g0180others(17): Show | 21 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.657+166_657+168del others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | |||||
| chr12:27494487
|
TTTATTA | T | 80 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(77): Show | 91 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.657+163_657+168del others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | |||||
| chr12:27494487
|
TTTATTAT others(2): Show |
T | 43 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(40): Show | 48 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.657+160_657+168del others(9): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | |||||
| chr12:27494544
|
A | C | 6 | a0002c0007t0001g0023a0002c0007t0001g0025a0002c0007t0001g0026others(3): Show | 6 | HG00741.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+188A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27494544 | ||||||
| chr12:27494744
|
T | A | 19 | a0000c0006t0005g0015a0000c0006t0005g0166a0000c0006t0005g0167others(16): Show | 21 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.657+388T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27494744 | ||||||
| chr12:27495023
|
T | A | 2 | a0002c0016t0001g0239a0002c0016t0001g0315 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.658-657T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495023 | ||||||
| chr12:27495192
|
G | A | 10 | a0001c0001t0001g0266a0001c0001t0001g0296a0002c0003t0003g0005others(7): Show | 12 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.658-488G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495192 | ||||||
| chr12:27495478
|
C | T | 68 | a0003c0002t0001g0249a0003c0002t0002g0001a0003c0002t0002g0003others(65): Show | 78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.658-202C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495478 | ||||||
| chr12:27495522
|
C | G | 46 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(43): Show | 51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.658-158C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495522 | ||||||
| chr12:27495560
|
G | A | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.658-120G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495560 | ||||||
| chr12:27495891
|
A | T | 68 | a0003c0002t0001g0249a0003c0002t0002g0001a0003c0002t0002g0003others(65): Show | 78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.833+36A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27495891 | ||||||
| chr12:27495998
|
T | C | 5 | a0002c0005t0001g0027a0002c0005t0003g0329a0002c0005t0004g0280others(2): Show | 5 | HG02145.hp1 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.833+143T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27495998 | ||||||
| chr12:27496061
|
T | C | 1 | a0002c0003t0003g0132 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.833+206T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496061 | ||||||
| chr12:27496148
|
A | G | 1 | a0002c0007t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.833+293A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496148 | ||||||
| chr12:27496312
|
C | G | 20 | a0002c0005t0001g0018a0002c0005t0001g0027a0002c0005t0003g0329others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.833+457C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496312 | ||||||
| chr12:27496390
|
A | C | 68 | a0003c0002t0001g0249a0003c0002t0002g0001a0003c0002t0002g0003others(65): Show | 78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.833+535A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496390 | ||||||
| chr12:27496407
|
A | G | 1 | a0001c0001t0004g0270 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.833+552A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496407 | ||||||
| chr12:27496621
|
G | A | 44 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(41): Show | 49 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.833+766G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496621 | ||||||
| chr12:27496636
|
C | T | 2 | a0003c0002t0002g0098a0003c0002t0002g0099 | 2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.833+781C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496636 | ||||||
| chr12:27496798
|
G | T | 4 | a0001c0004t0001g0264a0001c0004t0002g0087a0001c0004t0004g0269others(1): Show | 4 | HG01243.hp2 HG01433.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.833+943G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496798 | ||||||
| chr12:27496867
|
G | A | 2 | a0006c0013t0001g0323a0006c0013t0002g0330 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.833+1012G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496867 | ||||||
| chr12:27496924
|
G | A | 66 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(63): Show | 71 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.833+1069G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496924 | ||||||
| chr12:27496977
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.833+1122G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496977 | ||||||
| chr12:27497174
|
G | C | 1 | a0002c0003t0003g0143 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.833+1319G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497174 | ||||||
| chr12:27497278
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0265 | 2 | HG03688.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.833+1423T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497278 | ||||||
| chr12:27497360
|
G | C | 68 | a0003c0002t0001g0249a0003c0002t0002g0001a0003c0002t0002g0003others(65): Show | 78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.833+1505G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497360 | ||||||
| chr12:27497372
|
A | C | 3 | a0001c0004t0001g0264a0001c0004t0002g0087a0001c0004t0004g0278 | 3 | HG01433.hp1 HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.833+1517A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497372 | ||||||
| chr12:27497498
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0165others(6): Show | 13 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.833+1643C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497498 | ||||||
| chr12:27497499
|
G | A | 1 | a0002c0005t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.833+1644G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497499 | ||||||
| chr12:27497711
|
T | C | 134 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(131): Show | 149 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.833+1856T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497711 | ||||||
| chr12:27497732
|
C | CA | 16 | a0001c0001t0001g0262a0001c0001t0001g0265a0001c0001t0001g0272others(13): Show | 17 | HG00642.hp2 HG01106.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.833+1895dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27497732 | |||||
| chr12:27497732
|
C | CAAAA | 48 | a0003c0002t0002g0001a0003c0002t0002g0003a0003c0002t0002g0008others(45): Show | 58 | HG00544.hp1 HG00733.hp2 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.833+1892_833+1895d others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27497732 | |||||
| chr12:27497732
|
C | CAAAAA | 14 | a0003c0002t0001g0249a0003c0002t0002g0066a0003c0002t0002g0078others(11): Show | 14 | HG00558.hp2 HG03239.hp1 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.833+1891_833+1895d others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27497732 | |||||
| chr12:27497732
|
CA | C | 10 | a0001c0001t0001g0181a0001c0001t0001g0231a0001c0001t0001g0271others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.833+1895delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27497732 | |||||
| chr12:27497790
|
G | A | 1 | a0001c0008t0002g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.833+1935G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497790 | ||||||
| chr12:27497819
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.833+1964A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497819 | ||||||
| chr12:27498095
|
T | C | 19 | a0002c0005t0001g0018a0002c0005t0001g0027a0002c0005t0003g0329others(16): Show | 19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.833+2240T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498095 | ||||||
| chr12:27498100
|
A | C | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.833+2245A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498100 | ||||||
| chr12:27498146
|
C | T | 1 | a0001c0001t0002g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.833+2291C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498146 | ||||||
| chr12:27498158
|
A | G | 1 | a0001c0008t0002g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.833+2303A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498158 | ||||||
| chr12:27498218
|
T | C | 134 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(131): Show | 149 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.833+2363T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498218 | ||||||
| chr12:27498366
|
A | T | 134 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(131): Show | 149 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.833+2511A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498366 | ||||||
| chr12:27498520
|
G | A | 19 | a0002c0005t0001g0018a0002c0005t0001g0027a0002c0005t0003g0329others(16): Show | 19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.833+2665G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498520 | ||||||
| chr12:27498603
|
G | A | 2 | a0002c0003t0003g0159a0002c0003t0003g0160 | 2 | NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.833+2748G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498603 | ||||||
| chr12:27498659
|
T | A | 3 | a0001c0004t0001g0162a0001c0004t0001g0189a0001c0004t0001g0214 | 3 | HG00099.hp1 HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.833+2804T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498659 | ||||||
| chr12:27498982
|
T | C | 4 | a0003c0009t0001g0207a0003c0009t0001g0253a0003c0009t0004g0172others(1): Show | 4 | HG02300.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.834-2941T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498982 | ||||||
| chr12:27499096
|
C | G | 19 | a0002c0005t0001g0018a0002c0005t0001g0027a0002c0005t0003g0329others(16): Show | 19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.834-2827C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499096 | ||||||
| chr12:27499194
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.834-2729G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499194 | ||||||
| chr12:27499717
|
A | G | 19 | a0002c0005t0001g0018a0002c0005t0001g0027a0002c0005t0003g0329others(16): Show | 19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.834-2206A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499717 | ||||||
| chr12:27499855
|
G | A | 4 | a0002c0003t0003g0153a0002c0003t0003g0154a0002c0003t0003g0155others(1): Show | 4 | HG03239.hp2 HG03688.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.834-2068G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499855 | ||||||
| chr12:27499860
|
T | C | 1 | a0008c0018t0001g0267 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.834-2063T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499860 | ||||||
| chr12:27499870
|
T | A | 1 | a0002c0007t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.834-2053T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499870 | ||||||
| chr12:27500126
|
A | C | 134 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(131): Show | 149 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.834-1797A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500126 | ||||||
| chr12:27500148
|
AT | A | 90 | a0001c0001t0001g0164a0001c0001t0002g0326a0001c0001t0002g0327others(87): Show | 100 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.834-1766delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27500148 | |||||
| chr12:27500243
|
T | C | 2 | a0002c0016t0001g0239a0002c0016t0001g0315 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.834-1680T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500243 | ||||||
| chr12:27500286
|
G | A | 2 | a0001c0001t0001g0254a0002c0005t0002g0120 | 2 | NA19043.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.834-1637G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500286 | ||||||
| chr12:27500487
|
CAAATTAT others(14): Show |
C | 68 | a0003c0002t0001g0249a0003c0002t0002g0001a0003c0002t0002g0003others(65): Show | 78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.834-1434_834-1414d others(23): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27500487 | |||||
| chr12:27500635
|
C | T | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.834-1288C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500635 | ||||||
| chr12:27500636
|
G | A | 2 | a0006c0013t0001g0323a0006c0013t0002g0330 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.834-1287G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500636 | ||||||
| chr12:27500689
|
C | T | 1 | a0002c0003t0003g0130 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.834-1234C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500689 | ||||||
| chr12:27500838
|
C | T | 19 | a0002c0005t0001g0018a0002c0005t0001g0027a0002c0005t0003g0329others(16): Show | 19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.834-1085C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500838 | ||||||
| chr12:27500885
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.834-1038A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500885 | ||||||
| chr12:27501078
|
A | G | 1 | a0003c0002t0002g0107 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.834-845A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501078 | ||||||
| chr12:27501114
|
G | T | 1 | a0001c0004t0001g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.834-809G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501114 | ||||||
| chr12:27501379
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.834-544G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501379 | ||||||
| chr12:27501382
|
G | C | 1 | a0001c0004t0001g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.834-541G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501382 | ||||||
| chr12:27501386
|
A | T | 1 | a0001c0001t0002g0079 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.834-537A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501386 | ||||||
| chr12:27501415
|
C | CA | 33 | a0001c0001t0001g0086a0001c0001t0001g0200a0001c0001t0002g0064others(30): Show | 36 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.834-486dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | |||||
| chr12:27501415
|
C | CAA | 11 | a0001c0008t0002g0050a0002c0005t0001g0018a0002c0005t0004g0280others(8): Show | 11 | HG01070.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.834-487_834-486dup others(2): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | |||||
| chr12:27501415
|
CA | C | 24 | a0001c0001t0001g0179a0001c0001t0002g0007a0001c0001t0002g0036others(21): Show | 25 | HG00544.hp2 HG01255.hp2 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.834-486delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | |||||
| chr12:27501415
|
CAA | C | 43 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00323.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.834-487_834-486del others(2): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | |||||
| chr12:27501415
|
CAAA | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 89 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.834-488_834-486del others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | |||||
| chr12:27501426
|
A | AC | 18 | a0002c0003t0001g0288a0002c0003t0003g0005a0002c0003t0003g0011others(15): Show | 21 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.834-497_834-496ins others(1): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501426 | ||||||
| chr12:27501430
|
A | AC | 26 | a0001c0012t0001g0034a0001c0012t0001g0211a0002c0003t0001g0197others(23): Show | 28 | HG00642.hp2 HG01884.hp2 HG02004.hp1 others(25): Show |
intron_variant | MODIFIER | c.834-493_834-492ins others(1): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501430 | ||||||
| chr12:27501430
|
A | C | 24 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0004t0001g0264others(21): Show | 27 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.834-493A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501430 | ||||||
| chr12:27501434
|
A | C | 76 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0171others(73): Show | 83 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.834-489A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501434 | ||||||
| chr12:27501438
|
C | A | 86 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0200others(83): Show | 96 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.834-485C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501438 | ||||||
| chr12:27501596
|
A | C | 71 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0200others(68): Show | 81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.834-327A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501596 | ||||||
| chr12:27501613
|
A | C | 71 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0200others(68): Show | 81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.834-310A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501613 | ||||||
| chr12:27501909
|
T | C | 1 | a0002c0019t0004g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.834-14T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501909 |