Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10592 |
|---|---|
| ensemblid | ENSG00000136824.19 |
| hgncid | 14011 |
| symbol | SMC2 |
| name | structural maintenance of chromosomes 2 |
| refseq_nuc | NM_006444.3 |
| refseq_prot | NP_006435.2 |
| ensembl_nuc | ENST00000374793.8 |
| ensembl_prot | ENSP00000363925.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 104094309 |
| end | 104141419 |
| strand | + |
| ver | v1.2 |
| region | chr9:104094309-104141419 |
| region5000 | chr9:104089309-104146419 |
| regionname0 | SMC2_chr9_104094309_104141419 |
| regionname5000 | SMC2_chr9_104089309_104146419 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1197 | 265 | 79 | 58 | 71 | 12 | 43 | 47 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0002 | 0/0 | 1197 | 4 | 1 | 2 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0003 | 0/0 | 1197 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0004 | 0/0 | 1197 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0005 | 0/0 | 1197 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0006 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3594 | 122 | 36 | 31 | 29 | 5 | 20 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0002 | 1/0 | 3594 | 109 | 16 | 26 | 36 | 7 | 23 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0003 | 0/0 | 3594 | 27 | 22 | 0 | 5 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0004 | 0/0 | 3594 | 4 | 4 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0005 | 0/0 | 3594 | 4 | 1 | 2 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0006 | 0/0 | 3594 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0007 | 0/0 | 3594 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0008 | 0/0 | 3594 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0009 | 0/0 | 3594 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0010 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0011 | 0/0 | 3594 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0012 | 0/0 | 3594 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| c0013 | 0/0 | 3594 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2335 | 89 | 19 | 25 | 24 | 5 | 15 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0002 | 0/0 | 2335 | 70 | 21 | 17 | 19 | 0 | 13 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0003 | 0/1 | 2335 | 21 | 2 | 10 | 0 | 3 | 5 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0004 | 0/0 | 2337 | 18 | 18 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0005 | 0/0 | 2335 | 17 | 2 | 1 | 9 | 1 | 4 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0006 | 0/0 | 2335 | 12 | 0 | 4 | 7 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0007 | 0/0 | 2335 | 7 | 7 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0008 | 0/0 | 2337 | 5 | 0 | 0 | 5 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0009 | 0/0 | 2335 | 3 | 3 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0010 | 0/0 | 2335 | 3 | 0 | 0 | 3 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0011 | 0/0 | 2335 | 3 | 0 | 0 | 0 | 1 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0012 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0013 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0014 | 0/0 | 2281 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0015 | 0/0 | 2335 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0016 | 0/0 | 2335 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0017 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0018 | 0/0 | 2335 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0019 | 0/0 | 2335 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0020 | 0/0 | 2335 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0021 | 0/0 | 2335 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0022 | 0/0 | 2335 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0023 | 0/0 | 2335 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0024 | 0/0 | 2335 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0025 | 0/0 | 2335 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0026 | 0/0 | 2335 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0027 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0028 | 0/0 | 2335 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0029 | 0/0 | 2335 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0030 | 0/0 | 2335 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0031 | 0/0 | 2335 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0032 | 0/0 | 2335 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0033 | 0/0 | 2335 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0034 | 0/0 | 2335 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0035 | 0/0 | 2335 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| t0036 | 0/0 | 2335 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 21 | 3 | 2 | 12 | 1 | 3 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0002 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0003 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0004 | 0/1 | 8 | 0 | 4 | 0 | 1 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0005 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0008 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0009 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0012 | 1/0 | 4 | 0 | 1 | 0 | 0 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3594 | 122 | 36 | 31 | 29 | 5 | 20 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002 | 1/0 | 3594 | 109 | 16 | 26 | 36 | 7 | 23 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0003 | 0/0 | 3594 | 27 | 22 | 0 | 5 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0007 | 0/0 | 3594 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0008 | 0/0 | 3594 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0010 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0011 | 0/0 | 3594 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0013 | 0/0 | 3594 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0002c0005 | 0/0 | 3594 | 4 | 1 | 2 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0003c0004 | 0/0 | 3594 | 4 | 4 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0004c0009 | 0/0 | 3594 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0005c0006 | 0/0 | 3594 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0006c0012 | 0/0 | 3594 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5928 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0002 | 0/0 | 5928 | 65 | 19 | 15 | 19 | 0 | 12 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0003 | 0/1 | 5928 | 21 | 2 | 10 | 0 | 3 | 5 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0005 | 0/0 | 5928 | 15 | 2 | 1 | 8 | 1 | 3 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0007 | 0/0 | 5928 | 7 | 7 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0016 | 0/0 | 5928 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0019 | 0/0 | 5928 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0026 | 0/0 | 5928 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0028 | 0/0 | 5928 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0029 | 0/0 | 5928 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0030 | 0/0 | 5928 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0031 | 0/0 | 5928 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0032 | 0/0 | 5928 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0033 | 0/0 | 5928 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0034 | 0/0 | 5928 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0035 | 0/0 | 5928 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0001t0036 | 0/0 | 5928 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0001 | 1/0 | 5928 | 82 | 16 | 22 | 23 | 5 | 15 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0005 | 0/0 | 5928 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0006 | 0/0 | 5928 | 12 | 0 | 4 | 7 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0010 | 0/0 | 5928 | 3 | 0 | 0 | 3 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0011 | 0/0 | 5928 | 3 | 0 | 0 | 0 | 1 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0014 | 0/0 | 5874 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0018 | 0/0 | 5928 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0020 | 0/0 | 5928 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0021 | 0/0 | 5928 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0022 | 0/0 | 5928 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0023 | 0/0 | 5928 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0002t0024 | 0/0 | 5928 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0003t0004 | 0/0 | 5930 | 18 | 18 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0003t0008 | 0/0 | 5930 | 5 | 0 | 0 | 5 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0003t0013 | 0/0 | 5930 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0003t0017 | 0/0 | 5930 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0003t0027 | 0/0 | 5930 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0007t0001 | 0/0 | 5928 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0008t0015 | 0/0 | 5928 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0010t0002 | 0/0 | 5928 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0011t0005 | 0/0 | 5928 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0001c0013t0001 | 0/0 | 5928 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0002c0005t0002 | 0/0 | 5928 | 4 | 1 | 2 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0003c0004t0009 | 0/0 | 5928 | 3 | 3 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0003c0004t0025 | 0/0 | 5928 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0004c0009t0001 | 0/0 | 5928 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0005c0006t0012 | 0/0 | 5930 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| a0006c0012t0001 | 0/0 | 5928 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | copy fasta | chr9 | 104089309 | 104146419 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0002 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0004 | 0/1 | 8 | 0 | 4 | 0 | 1 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0007g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0016g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0019g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0026g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0028g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0029g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0030g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0031g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0032g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0033g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0034g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0035g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0001t0036g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0001 | 0/0 | 12 | 3 | 1 | 5 | 1 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0012 | 1/0 | 3 | 0 | 1 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0006g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0010g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0010g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0011g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0011g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0014g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0020g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0021g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0022g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0023g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0002t0024g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0013g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0017g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0003t0027g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0007t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0008t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0008t0015g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0010t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0011t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0001c0013t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0002c0005t0002g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0002c0005t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0003c0004t0009g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0003c0004t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0003c0004t0025g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0004c0009t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0005c0006t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0005c0006t0012g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| a0006c0012t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0124 | EUR | GBR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00140 | hp2 | a0001 | c0002 | t0011 | g0137 | EUR | GBR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0020 | EUR | FIN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0065 | EUR | FIN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00323 | hp1 | a0001 | c0001 | t0033 | g0061 | EUR | FIN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00609 | hp1 | a0001 | c0011 | t0005 | g0062 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00609 | hp2 | a0001 | c0002 | t0010 | g0001 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00621 | hp1 | a0001 | c0001 | t0026 | g0014 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0064 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01074 | hp1 | a0001 | c0001 | t0034 | g0003 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01099 | hp1 | a0001 | c0002 | t0006 | g0119 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01099 | hp2 | a0004 | c0009 | t0001 | g0034 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01106 | hp1 | a0001 | c0001 | t0035 | g0101 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01168 | hp2 | a0001 | c0001 | t0016 | g0025 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0025 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01192 | hp2 | a0004 | c0009 | t0001 | g0034 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01257 | hp1 | a0002 | c0005 | t0002 | g0015 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01258 | hp2 | a0002 | c0005 | t0002 | g0015 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01515 | hp1 | a0001 | c0002 | t0021 | g0020 | EUR | IBS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0126 | EUR | IBS | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01891 | hp2 | a0001 | c0003 | t0004 | g0054 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01978 | hp1 | a0001 | c0002 | t0006 | g0138 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01993 | hp2 | a0001 | c0002 | t0006 | g0001 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02004 | hp2 | a0001 | c0002 | t0006 | g0143 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02015 | hp1 | a0001 | c0002 | t0006 | g0001 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02055 | hp2 | a0001 | c0001 | t0030 | g0091 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02071 | hp2 | a0001 | c0002 | t0010 | g0005 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02132 | hp1 | a0001 | c0002 | t0006 | g0001 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02132 | hp2 | a0001 | c0003 | t0008 | g0047 | EAS | KHV | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02280 | hp2 | a0001 | c0003 | t0004 | g0023 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02293 | hp2 | a0001 | c0013 | t0001 | g0134 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02615 | hp1 | a0001 | c0001 | t0029 | g0104 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02622 | hp2 | a0001 | c0003 | t0004 | g0037 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02630 | hp2 | a0001 | c0001 | t0028 | g0116 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02698 | hp1 | a0001 | c0002 | t0020 | g0127 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02717 | hp2 | a0001 | c0003 | t0013 | g0050 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02738 | hp1 | a0001 | c0002 | t0024 | g0009 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02809 | hp1 | a0003 | c0004 | t0009 | g0040 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0068 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02818 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02818 | hp2 | a0005 | c0006 | t0012 | g0039 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02895 | hp2 | a0001 | c0003 | t0004 | g0051 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0022 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02922 | hp2 | a0001 | c0007 | t0001 | g0041 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02965 | hp1 | a0001 | c0003 | t0004 | g0053 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02970 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03041 | hp2 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03130 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03130 | hp2 | a0005 | c0006 | t0012 | g0038 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03195 | hp2 | a0001 | c0008 | t0015 | g0113 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03209 | hp1 | a0001 | c0003 | t0004 | g0023 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03225 | hp1 | a0001 | c0008 | t0015 | g0114 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03225 | hp2 | a0003 | c0004 | t0009 | g0024 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03239 | hp1 | a0001 | c0002 | t0023 | g0153 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03453 | hp1 | a0001 | c0003 | t0027 | g0056 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03486 | hp2 | a0003 | c0004 | t0025 | g0072 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03490 | hp1 | a0001 | c0002 | t0011 | g0001 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03492 | hp2 | a0001 | c0002 | t0011 | g0145 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0042 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03516 | hp2 | a0002 | c0005 | t0002 | g0105 | AFR | ESN | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03540 | hp2 | a0001 | c0003 | t0013 | g0048 | AFR | GWD | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0055 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0060 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03654 | hp2 | a0001 | c0002 | t0022 | g0012 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | STU | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | STU | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0148 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03942 | hp2 | a0002 | c0005 | t0002 | g0015 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | STU | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0069 | SAS | STU | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0007 | SAS | BEB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | STU | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG04228 | hp1 | a0001 | c0002 | t0006 | g0166 | SAS | STU | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG04228 | hp2 | a0001 | c0002 | t0005 | g0063 | SAS | STU | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18522 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | YRI | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | YRI | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18939 | hp2 | a0001 | c0002 | t0006 | g0120 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18941 | hp1 | a0001 | c0002 | t0006 | g0001 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18945 | hp1 | a0001 | c0003 | t0008 | g0044 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18951 | hp1 | a0001 | c0002 | t0018 | g0001 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18951 | hp2 | a0001 | c0003 | t0008 | g0043 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18954 | hp1 | a0001 | c0002 | t0006 | g0118 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18961 | hp1 | a0001 | c0002 | t0014 | g0001 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18961 | hp2 | a0001 | c0003 | t0008 | g0046 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18965 | hp2 | a0001 | c0002 | t0006 | g0139 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19004 | hp2 | a0001 | c0003 | t0008 | g0045 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19012 | hp1 | a0001 | c0002 | t0010 | g0158 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19030 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | LWK | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19030 | hp2 | a0003 | c0004 | t0009 | g0024 | AFR | LWK | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19043 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | LWK | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19043 | hp2 | a0001 | c0003 | t0017 | g0049 | AFR | LWK | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19066 | hp2 | a0001 | c0002 | t0006 | g0121 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19074 | hp2 | a0001 | c0002 | t0014 | g0001 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19076 | hp1 | a0006 | c0012 | t0001 | g0160 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19086 | hp2 | a0001 | c0001 | t0032 | g0007 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | YRI | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | YRI | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA20129 | hp1 | a0001 | c0003 | t0004 | g0052 | AFR | ASW | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ASW | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0018 | EUR | TSI | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0073 | EUR | TSI | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | TSI | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG01123 | hp2 | a0001 | c0001 | t0019 | g0159 | AMR | CLM | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0100 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG06807 | hp1 | a0001 | c0001 | t0036 | g0066 | AFR | USA | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| HG06807 | hp2 | a0001 | c0001 | t0031 | g0083 | AFR | USA | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA20300 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | USA | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | USA | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA21309 | hp1 | a0001 | c0010 | t0002 | g0112 | AFR | LWK | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0004 | REF | REF | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0012 | REF | REF | SMC2_chr9_104089309_104146419 | SMC2 | chr9 | 104089309 | 104146419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:104095548
|
C | G | 1 | a0004 | 2 | HG01099.hp2 HG01192.hp2 |
missense_variant | MODERATE | c.164C>G | p.Ser55Cys | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 2/25 | 394/5928 | 164/3594 | 55/1197 | chr9 | 104095548 | ||
| chr9:104100424
|
A | T | 1 | a0006 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.627A>T | p.Lys209Asn | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/25 | 857/5928 | 627/3594 | 209/1197 | chr9 | 104100424 | ||
| chr9:104102526
|
G | A | 1 | a0005 | 2 | HG02818.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.973G>A | p.Ala325Thr | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/25 | 1203/5928 | 973/3594 | 325/1197 | chr9 | 104102526 | ||
| chr9:104127290
|
C | T | 1 | a0002 | 4 | HG01257.hp1 HG01258.hp2 HG03516.hp2 others(1): Show |
missense_variant | MODERATE | c.2600C>T | p.Ser867Leu | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/25 | 2830/5928 | 2600/3594 | 867/1197 | chr9 | 104127290 | ||
| chr9:104134518
|
A | G | 1 | a0003 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.3212A>G | p.Lys1071Arg | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/25 | 3442/5928 | 3212/3594 | 1071/1197 | chr9 | 104134518 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:104098505
|
A | G | 1 | a0001c0013 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.378A>G | p.Arg126Arg | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/25 | 608/5928 | 378/3594 | 126/1197 | chr9 | 104098505 | ||
| chr9:104111667
|
T | C | 1 | a0001c0007 | 2 | HG02922.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.1107T>C | p.Asp369Asp | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/25 | 1337/5928 | 1107/3594 | 369/1197 | chr9 | 104111667 | ||
| chr9:104111670
|
T | G | 1 | a0001c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1110T>G | p.Ala370Ala | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/25 | 1340/5928 | 1110/3594 | 370/1197 | chr9 | 104111670 | ||
| chr9:104111754
|
T | C | 1 | a0001c0011 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.1194T>C | p.Leu398Leu | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/25 | 1424/5928 | 1194/3594 | 398/1197 | chr9 | 104111754 | ||
| chr9:104126697
|
C | T | 2 | a0001c0003a0005c0006 | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
synonymous_variant | LOW | c.2508C>T | p.Tyr836Tyr | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/25 | 2738/5928 | 2508/3594 | 836/1197 | chr9 | 104126697 | ||
| chr9:104134528
|
G | A | 9 | a0001c0001a0001c0003a0001c0007others(6): Show | 165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
synonymous_variant | LOW | c.3222G>A | p.Leu1074Leu | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/25 | 3452/5928 | 3222/3594 | 1074/1197 | chr9 | 104134528 | ||
| chr9:104139225
|
A | G | 2 | a0001c0003a0005c0006 | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
synonymous_variant | LOW | c.3504A>G | p.Val1168Val | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 3734/5928 | 3504/3594 | 1168/1197 | chr9 | 104139225 | ||
| chr9:104139240
|
A | G | 1 | a0001c0008 | 2 | HG03195.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.3519A>G | p.Gln1173Gln | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 3749/5928 | 3519/3594 | 1173/1197 | chr9 | 104139240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:104094329
|
C | T | 1 | a0001c0001t0036 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-210C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/25 | 1056 | chr9 | 104094329 | |||||
| chr9:104094352
|
C | T | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(19): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
5_prime_UTR_variant | MODIFIER | c.-187C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/25 | 1033 | chr9 | 104094352 | |||||
| chr9:104094377
|
G | T | 1 | a0001c0001t0035 | 1 | HG01106.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/25 | 1008 | chr9 | 104094377 | |||||
| chr9:104094396
|
C | G | 1 | a0001c0001t0016 | 2 | HG01168.hp2 HG01169.hp1 |
5_prime_UTR_variant | MODIFIER | c.-143C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/25 | 989 | chr9 | 104094396 | |||||
| chr9:104094410
|
T | G | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(24): Show | 159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
5_prime_UTR_variant | MODIFIER | c.-129T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/25 | 975 | chr9 | 104094410 | |||||
| chr9:104094411
|
T | C | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(24): Show | 159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
5_prime_UTR_variant | MODIFIER | c.-128T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/25 | 974 | chr9 | 104094411 | |||||
| chr9:104139457
|
G | A | 2 | a0003c0004t0009a0003c0004t0025 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*142G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 142 | chr9 | 104139457 | |||||
| chr9:104139539
|
A | C | 1 | a0001c0001t0034 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 224 | chr9 | 104139539 | |||||
| chr9:104139584
|
C | A | 1 | a0001c0002t0018 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 269 | chr9 | 104139584 | |||||
| chr9:104139596
|
A | C | 7 | a0001c0001t0005a0001c0001t0032a0001c0001t0033others(4): Show | 21 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*281A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 281 | chr9 | 104139596 | |||||
| chr9:104139767
|
C | G | 1 | a0001c0001t0031 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*452C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 452 | chr9 | 104139767 | |||||
| chr9:104139768
|
A | T | 2 | a0003c0004t0009a0003c0004t0025 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*453A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 453 | chr9 | 104139768 | |||||
| chr9:104139775
|
G | A | 3 | a0001c0003t0013a0001c0003t0017a0005c0006t0012 | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*460G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 460 | chr9 | 104139775 | |||||
| chr9:104139878
|
ATTTTAAT others(47): Show |
A | 1 | a0001c0002t0014 | 2 | NA18961.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*618_*671delTTTTAA others(48): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 618 | INFO_REALIGN_3_PRIME | chr9 | 104139878 | ||||
| chr9:104139932
|
G | A | 3 | a0001c0001t0003a0001c0001t0007a0001c0001t0016 | 30 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*617G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 617 | chr9 | 104139932 | |||||
| chr9:104139960
|
C | T | 1 | a0001c0002t0023 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 645 | chr9 | 104139960 | |||||
| chr9:104140018
|
A | G | 1 | a0001c0002t0022 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 703 | chr9 | 104140018 | |||||
| chr9:104140045
|
G | A | 1 | a0001c0001t0026 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*730G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 730 | chr9 | 104140045 | |||||
| chr9:104140053
|
C | T | 1 | a0001c0002t0006 | 12 | HG01099.hp1 HG01978.hp1 HG01993.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 738 | chr9 | 104140053 | |||||
| chr9:104140107
|
T | C | 6 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(3): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*792T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 792 | chr9 | 104140107 | |||||
| chr9:104140141
|
C | T | 12 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(9): Show | 106 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*826C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 826 | chr9 | 104140141 | |||||
| chr9:104140144
|
A | G | 5 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(2): Show | 28 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*829A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 829 | chr9 | 104140144 | |||||
| chr9:104140173
|
G | A | 6 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(3): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*858G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 858 | chr9 | 104140173 | |||||
| chr9:104140297
|
T | G | 1 | a0005c0006t0012 | 2 | HG02818.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*982T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 982 | chr9 | 104140297 | |||||
| chr9:104140340
|
C | T | 1 | a0001c0002t0021 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1025C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1025 | chr9 | 104140340 | |||||
| chr9:104140341
|
G | A | 6 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(3): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1026G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1026 | chr9 | 104140341 | |||||
| chr9:104140377
|
G | A | 6 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(3): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1062G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1062 | chr9 | 104140377 | |||||
| chr9:104140513
|
T | A | 1 | a0001c0003t0017 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1198T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1198 | chr9 | 104140513 | |||||
| chr9:104140523
|
T | C | 1 | a0001c0001t0032 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1208T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1208 | chr9 | 104140523 | |||||
| chr9:104140530
|
G | A | 1 | a0001c0001t0029 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1215G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1215 | chr9 | 104140530 | |||||
| chr9:104140722
|
T | TAC | 6 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(3): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1408_*1409insCA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1409 | INFO_REALIGN_3_PRIME | chr9 | 104140722 | ||||
| chr9:104140773
|
C | T | 6 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(3): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1458C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1458 | chr9 | 104140773 | |||||
| chr9:104140927
|
A | G | 1 | a0001c0002t0020 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1612A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1612 | chr9 | 104140927 | |||||
| chr9:104140967
|
T | C | 1 | a0001c0001t0030 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1652T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1652 | chr9 | 104140967 | |||||
| chr9:104140982
|
C | T | 6 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(3): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1667C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1667 | chr9 | 104140982 | |||||
| chr9:104141023
|
C | A | 6 | a0001c0003t0004a0001c0003t0008a0001c0003t0013others(3): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1708C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1708 | chr9 | 104141023 | |||||
| chr9:104141110
|
C | T | 1 | a0001c0003t0008 | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1795C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1795 | chr9 | 104141110 | |||||
| chr9:104141118
|
T | C | 1 | a0001c0001t0036 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1803T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1803 | chr9 | 104141118 | |||||
| chr9:104141142
|
T | C | 1 | a0001c0001t0033 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1827T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1827 | chr9 | 104141142 | |||||
| chr9:104141177
|
G | A | 1 | a0001c0001t0007 | 7 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1862G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1862 | chr9 | 104141177 | |||||
| chr9:104141185
|
A | G | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(11): Show | 108 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1870A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 1870 | chr9 | 104141185 | |||||
| chr9:104141384
|
T | A | 1 | a0001c0002t0010 | 3 | HG00609.hp2 HG02071.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2069T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 2069 | chr9 | 104141384 | |||||
| chr9:104141385
|
T | G | 1 | a0005c0006t0012 | 2 | HG02818.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2070T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 2070 | chr9 | 104141385 | |||||
| chr9:104141406
|
A | G | 1 | a0001c0002t0011 | 3 | HG00140.hp2 HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2091A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 25/25 | 2091 | chr9 | 104141406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:104094512
|
G | C | 106 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(103): Show | 164 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.-62+35G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094512 | ||||||
| chr9:104094525
|
T | TGGCGGGA | 3 | a0001c0003t0004g0037a0005c0006t0012g0038a0005c0006t0012g0039 | 3 | HG02622.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-62+69_-62+75dupAG others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 104094525 | |||||
| chr9:104094525
|
TGGCGGGA | T | 80 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(77): Show | 129 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-62+69_-62+75delAG others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 104094525 | |||||
| chr9:104094582
|
G | T | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-62+105G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094582 | ||||||
| chr9:104094629
|
C | T | 103 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(100): Show | 161 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-62+152C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094629 | ||||||
| chr9:104094671
|
C | T | 82 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(79): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-62+194C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094671 | ||||||
| chr9:104094691
|
G | C | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(99): Show | 159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-62+214G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094691 | ||||||
| chr9:104094747
|
A | G | 1 | a0001c0001t0003g0031 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-62+270A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094747 | ||||||
| chr9:104094757
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-62+280C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094757 | ||||||
| chr9:104094797
|
A | G | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(99): Show | 159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-62+320A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094797 | ||||||
| chr9:104094876
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-62+399G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094876 | ||||||
| chr9:104094898
|
G | C | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-62+421G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094898 | ||||||
| chr9:104094899
|
ATTGTGGA others(3): Show |
A | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(99): Show | 159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-62+423_-61-415del others(10): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094899 | ||||||
| chr9:104094929
|
G | A | 4 | a0001c0002t0006g0118a0001c0002t0006g0119a0001c0002t0006g0120others(1): Show | 4 | HG01099.hp1 NA18939.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.-61-395G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104094929 | ||||||
| chr9:104095029
|
G | A | 1 | a0001c0001t0016g0025 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-61-295G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104095029 | ||||||
| chr9:104095173
|
G | T | 2 | a0001c0008t0015g0113a0001c0008t0015g0114 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-61-151G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 1/24 | chr9 | 104095173 | ||||||
| chr9:104095627
|
G | A | 103 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(100): Show | 160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.168+75G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 2/24 | chr9 | 104095627 | ||||||
| chr9:104095756
|
C | T | 15 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(12): Show | 23 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(20): Show |
intron_variant | MODIFIER | c.168+204C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 2/24 | chr9 | 104095756 | ||||||
| chr9:104095876
|
T | G | 1 | a0001c0001t0003g0058 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.169-272T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 2/24 | chr9 | 104095876 | ||||||
| chr9:104095911
|
A | G | 103 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(100): Show | 160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.169-237A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 2/24 | chr9 | 104095911 | ||||||
| chr9:104095945
|
A | G | 1 | a0001c0010t0002g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.169-203A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 2/24 | chr9 | 104095945 | ||||||
| chr9:104096142
|
T | A | 1 | a0001c0001t0002g0057 | 1 | HG02071.hp1 | splice_region_variant&intron_variant | LOW | c.169-6T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 2/24 | chr9 | 104096142 | ||||||
| chr9:104096431
|
T | C | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.318+134T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104096431 | ||||||
| chr9:104096507
|
G | A | 103 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(100): Show | 160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.318+210G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104096507 | ||||||
| chr9:104096570
|
T | G | 21 | a0001c0001t0002g0014a0001c0001t0002g0057a0001c0001t0002g0059others(18): Show | 27 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.318+273T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104096570 | ||||||
| chr9:104096814
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.318+517C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104096814 | ||||||
| chr9:104096826
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.318+529G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104096826 | ||||||
| chr9:104096864
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.318+567G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104096864 | ||||||
| chr9:104096880
|
C | T | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.318+583C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104096880 | ||||||
| chr9:104096912
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.318+615C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104096912 | ||||||
| chr9:104097064
|
A | AT | 9 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(6): Show | 17 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.318+776dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097064 | |||||
| chr9:104097115
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.318+818C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097115 | ||||||
| chr9:104097119
|
G | GT | 26 | a0001c0001t0001g0122a0001c0001t0002g0102a0001c0001t0002g0103others(23): Show | 34 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.318+845dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097119 | |||||
| chr9:104097119
|
G | GTT | 19 | a0001c0001t0002g0014a0001c0001t0002g0057a0001c0001t0002g0059others(16): Show | 25 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.318+844_318+845dup others(2): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097119 | |||||
| chr9:104097119
|
G | GTTT | 5 | a0001c0001t0002g0071a0001c0001t0005g0068a0001c0001t0005g0069others(2): Show | 5 | HG00438.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+843_318+845dup others(3): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097119 | |||||
| chr9:104097119
|
GTT | G | 4 | a0001c0003t0004g0013a0001c0003t0004g0055a0003c0004t0009g0024others(1): Show | 7 | HG02572.hp2 HG02809.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+844_318+845del others(2): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097119 | |||||
| chr9:104097119
|
GTTT | G | 18 | a0001c0003t0004g0006a0001c0003t0004g0022a0001c0003t0004g0023others(15): Show | 24 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.318+843_318+845del others(3): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097119 | |||||
| chr9:104097128
|
T | G | 1 | a0001c0002t0006g0118 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.318+831T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097128 | ||||||
| chr9:104097142
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.318+845T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097142 | ||||||
| chr9:104097190
|
G | T | 1 | a0001c0001t0035g0101 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.318+893G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097190 | ||||||
| chr9:104097256
|
C | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.318+959C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097256 | ||||||
| chr9:104097262
|
A | G | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+965A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097262 | ||||||
| chr9:104097263
|
A | ATT | 18 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(15): Show | 26 | HG02132.hp2 HG02280.hp2 HG02572.hp2 others(23): Show |
intron_variant | MODIFIER | c.318+974_318+975dup others(2): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097263 | |||||
| chr9:104097273
|
G | T | 13 | a0001c0003t0004g0037a0001c0003t0004g0054a0001c0003t0008g0043others(10): Show | 13 | HG01891.hp2 HG02132.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.318+976G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097273 | ||||||
| chr9:104097353
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.318+1056G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097353 | ||||||
| chr9:104097420
|
TA | T | 86 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.319-1021delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097420 | |||||
| chr9:104097457
|
T | C | 86 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.319-989T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097457 | ||||||
| chr9:104097508
|
G | GAA | 15 | a0001c0001t0005g0007a0001c0001t0005g0026a0001c0001t0005g0027others(12): Show | 20 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.319-921_319-920dup others(2): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097508 | |||||
| chr9:104097508
|
GA | G | 7 | a0001c0001t0002g0102a0001c0003t0004g0053a0001c0007t0001g0041others(4): Show | 8 | HG01243.hp2 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.319-920delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097508 | |||||
| chr9:104097508
|
GAA | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(58): Show | 105 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.319-921_319-920del others(2): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097508 | |||||
| chr9:104097508
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0007g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.319-930_319-920del others(11): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 104097508 | |||||
| chr9:104097530
|
G | A | 86 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.319-916G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097530 | ||||||
| chr9:104097577
|
C | G | 1 | a0001c0001t0019g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.319-869C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097577 | ||||||
| chr9:104097592
|
C | G | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-854C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097592 | ||||||
| chr9:104097611
|
G | A | 5 | a0001c0007t0001g0041a0001c0007t0001g0042a0003c0004t0009g0024others(2): Show | 6 | HG02809.hp1 HG02922.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-835G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097611 | ||||||
| chr9:104097776
|
A | G | 1 | a0001c0001t0003g0031 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.319-670A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097776 | ||||||
| chr9:104097825
|
C | A | 5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-621C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097825 | ||||||
| chr9:104097843
|
A | C | 2 | a0005c0006t0012g0038a0005c0006t0012g0039 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.319-603A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097843 | ||||||
| chr9:104097878
|
A | G | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-568A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097878 | ||||||
| chr9:104097930
|
TA | T | 15 | a0001c0001t0005g0007a0001c0001t0005g0026a0001c0001t0005g0027others(12): Show | 20 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.319-515delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097930 | ||||||
| chr9:104097980
|
A | T | 1 | a0001c0003t0013g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.319-466A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104097980 | ||||||
| chr9:104098071
|
C | G | 1 | a0001c0002t0001g0169 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.319-375C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104098071 | ||||||
| chr9:104098287
|
C | T | 107 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(104): Show | 165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.319-159C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104098287 | ||||||
| chr9:104098302
|
C | T | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319-144C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 3/24 | chr9 | 104098302 | ||||||
| chr9:104098688
|
T | C | 65 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(62): Show | 110 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.441+120T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104098688 | ||||||
| chr9:104098792
|
G | A | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441+224G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104098792 | ||||||
| chr9:104098837
|
T | TA | 78 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(75): Show | 124 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.441+281dupA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr9 | 104098837 | |||||
| chr9:104098837
|
T | TAA | 4 | a0001c0001t0001g0122a0001c0001t0003g0073a0001c0001t0005g0060others(1): Show | 6 | HG01257.hp1 HG01258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+280_441+281dup others(2): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr9 | 104098837 | |||||
| chr9:104098837
|
TA | T | 15 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(12): Show | 23 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(20): Show |
intron_variant | MODIFIER | c.441+281delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr9 | 104098837 | |||||
| chr9:104098910
|
C | T | 86 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.441+342C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104098910 | ||||||
| chr9:104099000
|
G | A | 107 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(104): Show | 165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.441+432G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104099000 | ||||||
| chr9:104099001
|
C | T | 86 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.441+433C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104099001 | ||||||
| chr9:104099027
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.441+459G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104099027 | ||||||
| chr9:104099065
|
C | G | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+497C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104099065 | ||||||
| chr9:104099217
|
G | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-427G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104099217 | ||||||
| chr9:104099429
|
ATCATT | A | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-210_442-206del others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr9 | 104099429 | |||||
| chr9:104099518
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-126G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 4/24 | chr9 | 104099518 | ||||||
| chr9:104099741
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.480+59C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 5/24 | chr9 | 104099741 | ||||||
| chr9:104099765
|
A | T | 1 | a0001c0002t0010g0158 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.480+83A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 5/24 | chr9 | 104099765 | ||||||
| chr9:104099803
|
G | T | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+121G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 5/24 | chr9 | 104099803 | ||||||
| chr9:104099832
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.480+150A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 5/24 | chr9 | 104099832 | ||||||
| chr9:104099912
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.481-181T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 5/24 | chr9 | 104099912 | ||||||
| chr9:104099962
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.481-131C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 5/24 | chr9 | 104099962 | ||||||
| chr9:104099964
|
A | C | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.481-129A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 5/24 | chr9 | 104099964 | ||||||
| chr9:104099984
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.481-109C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 5/24 | chr9 | 104099984 | ||||||
| chr9:104100226
|
T | C | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.591+23T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 6/24 | chr9 | 104100226 | ||||||
| chr9:104100241
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.591+38G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 6/24 | chr9 | 104100241 | ||||||
| chr9:104100249
|
G | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.591+46G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 6/24 | chr9 | 104100249 | ||||||
| chr9:104100360
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.592-29G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 6/24 | chr9 | 104100360 | ||||||
| chr9:104100470
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.636+37G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104100470 | ||||||
| chr9:104100612
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.636+179G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104100612 | ||||||
| chr9:104100750
|
A | G | 1 | a0001c0002t0001g0157 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.636+317A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104100750 | ||||||
| chr9:104100766
|
C | T | 63 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(60): Show | 107 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.636+333C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104100766 | ||||||
| chr9:104100779
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.636+346C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104100779 | ||||||
| chr9:104100781
|
A | G | 63 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(60): Show | 107 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.636+348A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104100781 | ||||||
| chr9:104100831
|
T | C | 1 | a0001c0002t0001g0125 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.636+398T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104100831 | ||||||
| chr9:104100999
|
G | A | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+566G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104100999 | ||||||
| chr9:104101031
|
G | A | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0029g0104 | 3 | HG02615.hp1 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.636+598G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101031 | ||||||
| chr9:104101041
|
G | T | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.636+608G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101041 | ||||||
| chr9:104101057
|
C | T | 16 | a0001c0001t0002g0092a0001c0001t0003g0004a0001c0001t0003g0018others(13): Show | 30 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.636+624C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101057 | ||||||
| chr9:104101192
|
C | T | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.636+759C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101192 | ||||||
| chr9:104101233
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.637-727C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101233 | ||||||
| chr9:104101253
|
T | C | 1 | a0001c0002t0001g0161 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.637-707T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101253 | ||||||
| chr9:104101282
|
C | T | 1 | a0001c0002t0001g0156 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.637-678C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101282 | ||||||
| chr9:104101393
|
G | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.637-567G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101393 | ||||||
| chr9:104101446
|
A | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.637-514A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101446 | ||||||
| chr9:104101478
|
C | G | 2 | a0001c0002t0001g0036a0001c0002t0001g0155 | 3 | HG03017.hp1 HG03490.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.637-482C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101478 | ||||||
| chr9:104101567
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.637-393G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101567 | ||||||
| chr9:104101579
|
G | T | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.637-381G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101579 | ||||||
| chr9:104101627
|
C | T | 15 | a0001c0001t0005g0007a0001c0001t0005g0026a0001c0001t0005g0027others(12): Show | 20 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.637-333C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101627 | ||||||
| chr9:104101669
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.637-291A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101669 | ||||||
| chr9:104101736
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.637-224G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101736 | ||||||
| chr9:104101812
|
C | T | 2 | a0001c0001t0005g0060a0001c0001t0005g0065 | 2 | HG00280.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.637-148C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | chr9 | 104101812 | ||||||
| chr9:104101906
|
AT | A | 22 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(19): Show | 30 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.637-44delT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr9 | 104101906 | |||||
| chr9:104102256
|
G | A | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.870+63G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 8/24 | chr9 | 104102256 | ||||||
| chr9:104102289
|
C | T | 86 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.870+96C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 8/24 | chr9 | 104102289 | ||||||
| chr9:104102376
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.871-48G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 8/24 | chr9 | 104102376 | ||||||
| chr9:104102605
|
T | C | 2 | a0001c0001t0002g0077a0001c0001t0007g0100 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1020+32T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104102605 | ||||||
| chr9:104102746
|
C | A | 38 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(35): Show | 67 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1020+173C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104102746 | ||||||
| chr9:104102804
|
T | C | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+231T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104102804 | ||||||
| chr9:104103003
|
A | G | 1 | a0001c0001t0030g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1020+430A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103003 | ||||||
| chr9:104103017
|
T | C | 2 | a0001c0002t0001g0124a0001c0002t0001g0126 | 2 | HG00140.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1020+444T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103017 | ||||||
| chr9:104103157
|
A | G | 81 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(78): Show | 130 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1020+584A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103157 | ||||||
| chr9:104103159
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+586G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103159 | ||||||
| chr9:104103329
|
A | G | 1 | a0001c0001t0003g0031 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1020+756A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103329 | ||||||
| chr9:104103378
|
T | C | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1020+805T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103378 | ||||||
| chr9:104103389
|
C | G | 2 | a0001c0001t0002g0087a0001c0001t0002g0088 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1020+816C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103389 | ||||||
| chr9:104103398
|
A | G | 1 | a0001c0002t0001g0154 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1020+825A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103398 | ||||||
| chr9:104103410
|
A | T | 107 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(104): Show | 165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1020+837A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103410 | ||||||
| chr9:104103411
|
G | T | 107 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(104): Show | 165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1020+838G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103411 | ||||||
| chr9:104103431
|
T | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+858T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103431 | ||||||
| chr9:104103575
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+1002G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103575 | ||||||
| chr9:104103582
|
C | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1020+1009C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103582 | ||||||
| chr9:104103631
|
G | T | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+1058G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103631 | ||||||
| chr9:104103682
|
C | A | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+1109C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103682 | ||||||
| chr9:104103714
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+1141G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103714 | ||||||
| chr9:104103816
|
A | G | 2 | a0001c0008t0015g0113a0001c0008t0015g0114 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1020+1243A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103816 | ||||||
| chr9:104103882
|
T | C | 5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+1309T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103882 | ||||||
| chr9:104103896
|
A | G | 1 | a0001c0003t0008g0047 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1020+1323A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104103896 | ||||||
| chr9:104104122
|
C | T | 15 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(12): Show | 23 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(20): Show |
intron_variant | MODIFIER | c.1020+1549C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104122 | ||||||
| chr9:104104294
|
C | A | 1 | a0001c0001t0002g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1020+1721C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104294 | ||||||
| chr9:104104418
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+1845T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104418 | ||||||
| chr9:104104422
|
C | T | 107 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(104): Show | 165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1020+1849C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104422 | ||||||
| chr9:104104545
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+1972C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104545 | ||||||
| chr9:104104550
|
A | AG | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+1978dupG | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 104104550 | |||||
| chr9:104104616
|
A | G | 17 | a0001c0001t0005g0007a0001c0001t0005g0026a0001c0001t0005g0027others(14): Show | 22 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1020+2043A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104616 | ||||||
| chr9:104104619
|
G | A | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1020+2046G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104619 | ||||||
| chr9:104104623
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1020+2050T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104623 | ||||||
| chr9:104104796
|
G | A | 1 | a0001c0002t0001g0011 | 4 | HG02615.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020+2223G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104796 | ||||||
| chr9:104104818
|
T | C | 1 | a0001c0002t0020g0127 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1020+2245T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104818 | ||||||
| chr9:104104825
|
A | C | 82 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1020+2252A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104104825 | ||||||
| chr9:104105053
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+2480C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105053 | ||||||
| chr9:104105147
|
T | C | 1 | a0001c0002t0001g0128 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1020+2574T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105147 | ||||||
| chr9:104105309
|
A | T | 1 | a0001c0001t0029g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1020+2736A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105309 | ||||||
| chr9:104105381
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+2808G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105381 | ||||||
| chr9:104105418
|
T | A | 1 | a0001c0001t0030g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1020+2845T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105418 | ||||||
| chr9:104105497
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1020+2924G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105497 | ||||||
| chr9:104105661
|
T | G | 1 | a0001c0002t0001g0032 | 2 | HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1020+3088T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105661 | ||||||
| chr9:104105752
|
A | G | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1020+3179A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105752 | ||||||
| chr9:104105826
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1020+3253T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105826 | ||||||
| chr9:104105849
|
G | A | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1020+3276G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105849 | ||||||
| chr9:104105909
|
C | A | 7 | a0001c0001t0002g0008a0001c0001t0002g0016a0001c0001t0002g0078others(4): Show | 15 | HG00733.hp1 HG00735.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1020+3336C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105909 | ||||||
| chr9:104105909
|
C | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(53): Show | 92 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1020+3336C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104105909 | ||||||
| chr9:104106162
|
A | G | 81 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(78): Show | 130 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1020+3589A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106162 | ||||||
| chr9:104106333
|
C | G | 1 | a0001c0001t0003g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1020+3760C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106333 | ||||||
| chr9:104106363
|
A | T | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+3790A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106363 | ||||||
| chr9:104106550
|
C | T | 1 | a0001c0002t0023g0153 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1020+3977C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106550 | ||||||
| chr9:104106562
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+3989T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106562 | ||||||
| chr9:104106623
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+4050C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106623 | ||||||
| chr9:104106725
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+4152C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106725 | ||||||
| chr9:104106753
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+4180C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106753 | ||||||
| chr9:104106764
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1020+4191G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106764 | ||||||
| chr9:104106887
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1020+4314A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106887 | ||||||
| chr9:104106893
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+4320A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106893 | ||||||
| chr9:104106896
|
T | TA | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+4324dupA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 104106896 | |||||
| chr9:104106934
|
C | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1020+4361C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106934 | ||||||
| chr9:104106969
|
C | A | 14 | a0001c0001t0005g0007a0001c0001t0005g0026a0001c0001t0005g0027others(11): Show | 19 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.1020+4396C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106969 | ||||||
| chr9:104106984
|
C | T | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1020+4411C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106984 | ||||||
| chr9:104106988
|
T | A | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1020+4415T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104106988 | ||||||
| chr9:104107002
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+4429G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107002 | ||||||
| chr9:104107006
|
C | T | 1 | a0001c0001t0005g0060 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1020+4433C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107006 | ||||||
| chr9:104107226
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-4355A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107226 | ||||||
| chr9:104107231
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-4350C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107231 | ||||||
| chr9:104107249
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1021-4332C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107249 | ||||||
| chr9:104107315
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-4266A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107315 | ||||||
| chr9:104107381
|
C | A | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1021-4200C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107381 | ||||||
| chr9:104107522
|
CGCTGTTC others(7): Show |
C | 1 | a0001c0001t0005g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-4056_1021-404 others(18): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 104107522 | |||||
| chr9:104107545
|
G | C | 1 | a0001c0001t0002g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1021-4036G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107545 | ||||||
| chr9:104107643
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-3938C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107643 | ||||||
| chr9:104107668
|
C | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1021-3913C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107668 | ||||||
| chr9:104107792
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1021-3789C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107792 | ||||||
| chr9:104107818
|
T | C | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1021-3763T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107818 | ||||||
| chr9:104107846
|
T | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-3735T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107846 | ||||||
| chr9:104107880
|
G | T | 1 | a0001c0001t0005g0064 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1021-3701G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107880 | ||||||
| chr9:104107906
|
A | C | 64 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(61): Show | 108 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1021-3675A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104107906 | ||||||
| chr9:104108304
|
C | T | 162 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(159): Show | 251 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1021-3277C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108304 | ||||||
| chr9:104108383
|
G | A | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-3198G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108383 | ||||||
| chr9:104108441
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-3140C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108441 | ||||||
| chr9:104108451
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-3130A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108451 | ||||||
| chr9:104108496
|
C | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-3085C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108496 | ||||||
| chr9:104108528
|
C | T | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-3053C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108528 | ||||||
| chr9:104108566
|
C | T | 2 | a0005c0006t0012g0038a0005c0006t0012g0039 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1021-3015C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108566 | ||||||
| chr9:104108567
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1021-3014G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108567 | ||||||
| chr9:104108769
|
AATCCTAG others(5): Show |
A | 82 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1021-2809_1021-279 others(16): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 104108769 | |||||
| chr9:104108911
|
A | G | 1 | a0001c0001t0002g0080 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1021-2670A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108911 | ||||||
| chr9:104108917
|
C | T | 1 | a0001c0002t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1021-2664C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104108917 | ||||||
| chr9:104109180
|
A | T | 17 | a0001c0001t0005g0007a0001c0001t0005g0026a0001c0001t0005g0027others(14): Show | 22 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1021-2401A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109180 | ||||||
| chr9:104109265
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-2316G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109265 | ||||||
| chr9:104109326
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-2255A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109326 | ||||||
| chr9:104109363
|
A | G | 1 | a0001c0001t0005g0027 | 2 | NA18966.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1021-2218A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109363 | ||||||
| chr9:104109416
|
A | G | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1021-2165A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109416 | ||||||
| chr9:104109464
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-2117G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109464 | ||||||
| chr9:104109507
|
T | C | 64 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(61): Show | 108 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1021-2074T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109507 | ||||||
| chr9:104109594
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-1987G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109594 | ||||||
| chr9:104109595
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-1986C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109595 | ||||||
| chr9:104109811
|
T | G | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1021-1770T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109811 | ||||||
| chr9:104109936
|
T | G | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1021-1645T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104109936 | ||||||
| chr9:104110004
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-1577T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104110004 | ||||||
| chr9:104110013
|
T | C | 1 | a0001c0003t0013g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1021-1568T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104110013 | ||||||
| chr9:104110136
|
C | T | 1 | a0001c0001t0005g0027 | 2 | NA18966.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1021-1445C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104110136 | ||||||
| chr9:104110401
|
T | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(59): Show | 106 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1021-1180T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104110401 | ||||||
| chr9:104110401
|
T | C | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1021-1180T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104110401 | ||||||
| chr9:104110416
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-1165T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104110416 | ||||||
| chr9:104110467
|
GTGTTA | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-1107_1021-110 others(9): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 104110467 | |||||
| chr9:104110583
|
A | ATGT | 106 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(103): Show | 163 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1021-996_1021-994d others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 104110583 | |||||
| chr9:104110618
|
CTTTA | C | 162 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(159): Show | 251 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1021-958_1021-955d others(6): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 104110618 | |||||
| chr9:104110772
|
C | T | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1021-809C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104110772 | ||||||
| chr9:104111097
|
C | A | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1021-484C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104111097 | ||||||
| chr9:104111339
|
A | G | 1 | a0001c0003t0017g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1021-242A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104111339 | ||||||
| chr9:104111452
|
G | A | 1 | a0001c0003t0008g0043 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1021-129G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 9/24 | chr9 | 104111452 | ||||||
| chr9:104111822
|
G | C | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
splice_region_variant&intron_variant | LOW | c.1254+8G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104111822 | ||||||
| chr9:104111829
|
T | TA | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1254+16dupA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 104111829 | |||||
| chr9:104111932
|
G | A | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1254+118G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104111932 | ||||||
| chr9:104112048
|
G | A | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1254+234G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112048 | ||||||
| chr9:104112102
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1254+288C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112102 | ||||||
| chr9:104112296
|
C | A | 1 | a0001c0003t0008g0044 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1254+482C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112296 | ||||||
| chr9:104112343
|
C | G | 5 | a0001c0002t0001g0021a0001c0002t0001g0148a0001c0002t0001g0149others(2): Show | 7 | HG00438.hp1 HG00558.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+529C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112343 | ||||||
| chr9:104112394
|
C | A | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1254+580C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112394 | ||||||
| chr9:104112536
|
CTT | C | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1254+724_1254+725d others(4): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 104112536 | |||||
| chr9:104112685
|
A | G | 1 | a0001c0002t0001g0168 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1255-631A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112685 | ||||||
| chr9:104112776
|
T | C | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1255-540T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112776 | ||||||
| chr9:104112847
|
G | C | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1255-469G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112847 | ||||||
| chr9:104112879
|
C | T | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1255-437C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112879 | ||||||
| chr9:104112995
|
C | T | 1 | a0001c0002t0005g0063 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1255-321C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112995 | ||||||
| chr9:104112996
|
G | T | 103 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(100): Show | 160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1255-320G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104112996 | ||||||
| chr9:104113001
|
T | G | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1255-315T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104113001 | ||||||
| chr9:104113076
|
C | T | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1255-240C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 10/24 | chr9 | 104113076 | ||||||
| chr9:104113494
|
G | A | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1414+19G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 11/24 | chr9 | 104113494 | ||||||
| chr9:104113553
|
G | A | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1414+78G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 11/24 | chr9 | 104113553 | ||||||
| chr9:104113619
|
G | A | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1414+144G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 11/24 | chr9 | 104113619 | ||||||
| chr9:104113648
|
C | G | 1 | a0005c0006t0012g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1414+173C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 11/24 | chr9 | 104113648 | ||||||
| chr9:104113701
|
G | T | 23 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(20): Show | 31 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1414+226G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 11/24 | chr9 | 104113701 | ||||||
| chr9:104113948
|
A | G | 1 | a0003c0004t0009g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1415-16A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 11/24 | chr9 | 104113948 | ||||||
| chr9:104114167
|
A | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1532+86A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 12/24 | chr9 | 104114167 | ||||||
| chr9:104114334
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1532+253A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 12/24 | chr9 | 104114334 | ||||||
| chr9:104114464
|
A | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1533-227A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 12/24 | chr9 | 104114464 | ||||||
| chr9:104114546
|
A | T | 1 | a0001c0003t0004g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1533-145A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 12/24 | chr9 | 104114546 | ||||||
| chr9:104114569
|
AT | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1533-118delT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr9 | 104114569 | |||||
| chr9:104114572
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1533-119T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 12/24 | chr9 | 104114572 | ||||||
| chr9:104114621
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1533-70C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 12/24 | chr9 | 104114621 | ||||||
| chr9:104114854
|
A | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0090 | 3 | HG01891.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1671+25A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104114854 | ||||||
| chr9:104114958
|
A | C | 2 | a0001c0002t0001g0035a0001c0002t0001g0147 | 3 | HG02109.hp1 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1671+129A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104114958 | ||||||
| chr9:104115073
|
A | G | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671+244A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115073 | ||||||
| chr9:104115127
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1671+298C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115127 | ||||||
| chr9:104115219
|
C | T | 6 | a0001c0001t0003g0004a0001c0001t0003g0018a0001c0001t0003g0073others(3): Show | 15 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1671+390C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115219 | ||||||
| chr9:104115246
|
GT | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1671+427delT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 104115246 | |||||
| chr9:104115268
|
T | C | 5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671+439T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115268 | ||||||
| chr9:104115436
|
G | A | 16 | a0001c0001t0005g0007a0001c0001t0005g0026a0001c0001t0005g0027others(13): Show | 22 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1671+607G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115436 | ||||||
| chr9:104115460
|
A | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1671+631A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115460 | ||||||
| chr9:104115496
|
A | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1671+667A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115496 | ||||||
| chr9:104115512
|
TTGCGGTA others(3): Show |
T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1672-675_1672-666d others(12): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 104115512 | |||||
| chr9:104115580
|
A | T | 2 | a0001c0001t0001g0122a0001c0002t0001g0019 | 4 | HG01261.hp2 HG01433.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-620A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115580 | ||||||
| chr9:104115584
|
CA | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1672-605delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 104115584 | |||||
| chr9:104115596
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1672-604G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115596 | ||||||
| chr9:104115608
|
C | T | 1 | a0001c0001t0029g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1672-592C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115608 | ||||||
| chr9:104115631
|
T | C | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1672-569T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115631 | ||||||
| chr9:104115636
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1672-564A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115636 | ||||||
| chr9:104115658
|
G | A | 106 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(103): Show | 164 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1672-542G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115658 | ||||||
| chr9:104115749
|
G | GTAT | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1672-448_1672-446d others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 104115749 | |||||
| chr9:104115764
|
C | T | 2 | a0001c0008t0015g0113a0001c0008t0015g0114 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1672-436C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115764 | ||||||
| chr9:104115878
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1672-322C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104115878 | ||||||
| chr9:104116037
|
TCTC | T | 80 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(77): Show | 129 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1672-160_1672-158d others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 104116037 | |||||
| chr9:104116168
|
A | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1672-32A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104116168 | ||||||
| chr9:104116171
|
C | T | 1 | a0001c0003t0004g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1672-29C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 13/24 | chr9 | 104116171 | ||||||
| chr9:104116529
|
A | ATGTC | 20 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(17): Show | 28 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.1791+211_1791+214d others(6): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr9 | 104116529 | |||||
| chr9:104116534
|
C | T | 20 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(17): Show | 28 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.1791+215C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104116534 | ||||||
| chr9:104116558
|
TATCA | T | 106 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(103): Show | 164 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1791+244_1791+247d others(6): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr9 | 104116558 | |||||
| chr9:104116625
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1791+306C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104116625 | ||||||
| chr9:104116625
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(59): Show | 106 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1791+306C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104116625 | ||||||
| chr9:104117048
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1791+729G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117048 | ||||||
| chr9:104117081
|
C | G | 1 | a0001c0001t0002g0089 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1791+762C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117081 | ||||||
| chr9:104117126
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1791+807T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117126 | ||||||
| chr9:104117183
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1791+864C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117183 | ||||||
| chr9:104117286
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1792-885C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117286 | ||||||
| chr9:104117308
|
A | G | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1792-863A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117308 | ||||||
| chr9:104117419
|
T | C | 1 | a0001c0001t0003g0058 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1792-752T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117419 | ||||||
| chr9:104117554
|
C | T | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1792-617C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117554 | ||||||
| chr9:104117580
|
A | G | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1792-591A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117580 | ||||||
| chr9:104117642
|
G | A | 1 | a0001c0002t0006g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1792-529G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117642 | ||||||
| chr9:104117835
|
A | G | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1792-336A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117835 | ||||||
| chr9:104117865
|
C | G | 1 | a0001c0002t0001g0155 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1792-306C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117865 | ||||||
| chr9:104117895
|
G | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1792-276G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117895 | ||||||
| chr9:104117910
|
T | C | 2 | a0001c0003t0004g0022a0001c0003t0004g0055 | 3 | HG02896.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1792-261T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117910 | ||||||
| chr9:104117931
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1792-240T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117931 | ||||||
| chr9:104117969
|
A | G | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1792-202A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117969 | ||||||
| chr9:104117993
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1792-178G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117993 | ||||||
| chr9:104117994
|
T | G | 1 | a0001c0002t0011g0137 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1792-177T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104117994 | ||||||
| chr9:104118090
|
C | G | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-81C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104118090 | ||||||
| chr9:104118113
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1792-58C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 14/24 | chr9 | 104118113 | ||||||
| chr9:104118561
|
G | C | 3 | a0001c0002t0001g0129a0001c0002t0001g0162a0001c0002t0001g0163 | 3 | HG01258.hp1 HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1996+186G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118561 | ||||||
| chr9:104118562
|
G | A | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1996+187G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118562 | ||||||
| chr9:104118692
|
CCAGA | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1996+321_1996+324d others(6): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 104118692 | |||||
| chr9:104118715
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1996+340T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118715 | ||||||
| chr9:104118843
|
A | G | 1 | a0001c0001t0030g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1996+468A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118843 | ||||||
| chr9:104118856
|
A | T | 1 | a0001c0001t0002g0016 | 3 | HG02735.hp1 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1996+481A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118856 | ||||||
| chr9:104118887
|
A | G | 1 | a0001c0003t0004g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1996+512A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118887 | ||||||
| chr9:104118922
|
C | T | 1 | a0001c0003t0004g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1996+547C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118922 | ||||||
| chr9:104118985
|
C | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1996+610C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118985 | ||||||
| chr9:104118994
|
C | T | 9 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(6): Show | 17 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1996+619C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104118994 | ||||||
| chr9:104119072
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1996+697G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119072 | ||||||
| chr9:104119111
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1996+736C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119111 | ||||||
| chr9:104119121
|
C | T | 80 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(77): Show | 129 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1996+746C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119121 | ||||||
| chr9:104119435
|
T | C | 1 | a0003c0004t0009g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1997-592T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119435 | ||||||
| chr9:104119608
|
T | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1997-419T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119608 | ||||||
| chr9:104119612
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1997-415C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119612 | ||||||
| chr9:104119776
|
G | C | 1 | a0001c0002t0001g0155 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1997-251G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119776 | ||||||
| chr9:104119787
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1997-240G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119787 | ||||||
| chr9:104119886
|
G | A | 2 | a0001c0008t0015g0113a0001c0008t0015g0114 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1997-141G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 15/24 | chr9 | 104119886 | ||||||
| chr9:104120187
|
A | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+25A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120187 | ||||||
| chr9:104120229
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+67T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120229 | ||||||
| chr9:104120262
|
A | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+100A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120262 | ||||||
| chr9:104120346
|
G | T | 1 | a0001c0001t0002g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2132+184G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120346 | ||||||
| chr9:104120472
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+310C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120472 | ||||||
| chr9:104120587
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+425A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120587 | ||||||
| chr9:104120602
|
G | A | 1 | a0001c0001t0002g0028 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2132+440G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120602 | ||||||
| chr9:104120650
|
A | G | 18 | a0001c0001t0001g0122a0001c0001t0005g0007a0001c0001t0005g0026others(15): Show | 23 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2132+488A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120650 | ||||||
| chr9:104120804
|
T | G | 103 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(100): Show | 160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.2132+642T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120804 | ||||||
| chr9:104120876
|
A | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+714A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120876 | ||||||
| chr9:104120916
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+754C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120916 | ||||||
| chr9:104120937
|
T | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0131 | 2 | HG01255.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2132+775T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120937 | ||||||
| chr9:104120996
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+834G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104120996 | ||||||
| chr9:104121038
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+876C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121038 | ||||||
| chr9:104121075
|
A | AACACACG others(37): Show |
21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+925_2132+926i others(46): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr9 | 104121075 | |||||
| chr9:104121164
|
A | G | 22 | a0001c0001t0030g0091a0001c0003t0004g0006a0001c0003t0004g0013others(19): Show | 30 | HG01891.hp2 HG02055.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.2132+1002A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121164 | ||||||
| chr9:104121328
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+1166G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121328 | ||||||
| chr9:104121337
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+1175C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121337 | ||||||
| chr9:104121428
|
C | T | 2 | a0001c0002t0001g0130a0001c0002t0001g0131 | 2 | HG01255.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2132+1266C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121428 | ||||||
| chr9:104121495
|
CA | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+1342delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr9 | 104121495 | |||||
| chr9:104121531
|
T | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132+1369T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121531 | ||||||
| chr9:104121612
|
A | G | 1 | a0001c0002t0006g0120 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2132+1450A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121612 | ||||||
| chr9:104121616
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2132+1454A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121616 | ||||||
| chr9:104121651
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2133-1457G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121651 | ||||||
| chr9:104121761
|
G | GAGAT | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2133-1345_2133-134 others(8): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr9 | 104121761 | |||||
| chr9:104121785
|
G | T | 1 | a0001c0002t0001g0149 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2133-1323G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121785 | ||||||
| chr9:104121920
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2133-1188A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104121920 | ||||||
| chr9:104122068
|
A | G | 1 | a0001c0002t0001g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2133-1040A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122068 | ||||||
| chr9:104122281
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2133-827A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122281 | ||||||
| chr9:104122440
|
T | A | 1 | a0001c0002t0001g0125 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2133-668T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122440 | ||||||
| chr9:104122470
|
GT | G | 21 | a0001c0001t0002g0092a0001c0003t0004g0006a0001c0003t0004g0013others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2133-626delT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr9 | 104122470 | |||||
| chr9:104122535
|
T | C | 2 | a0001c0003t0013g0048a0001c0003t0013g0050 | 2 | HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2133-573T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122535 | ||||||
| chr9:104122563
|
A | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2133-545A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122563 | ||||||
| chr9:104122633
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2133-475A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122633 | ||||||
| chr9:104122658
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2133-450A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122658 | ||||||
| chr9:104122778
|
G | A | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2133-330G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122778 | ||||||
| chr9:104122855
|
A | G | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2133-253A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122855 | ||||||
| chr9:104122865
|
T | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0029g0104 | 3 | HG02615.hp1 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2133-243T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122865 | ||||||
| chr9:104122912
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2133-196A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122912 | ||||||
| chr9:104122962
|
C | T | 82 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.2133-146C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122962 | ||||||
| chr9:104122999
|
T | G | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2133-109T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104122999 | ||||||
| chr9:104123051
|
A | G | 64 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(61): Show | 108 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2133-57A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 16/24 | chr9 | 104123051 | ||||||
| chr9:104123236
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.2257+4A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123236 | ||||||
| chr9:104123315
|
A | G | 2 | a0001c0001t0003g0096a0001c0002t0001g0147 | 2 | HG02109.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2257+83A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123315 | ||||||
| chr9:104123335
|
A | G | 64 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(61): Show | 108 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2257+103A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123335 | ||||||
| chr9:104123454
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2257+222C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123454 | ||||||
| chr9:104123464
|
A | AACTTTT | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2257+232_2257+233i others(8): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123464 | ||||||
| chr9:104123509
|
A | G | 2 | a0001c0001t0028g0116a0001c0002t0001g0146 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2257+277A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123509 | ||||||
| chr9:104123636
|
T | C | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2257+404T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123636 | ||||||
| chr9:104123690
|
G | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2257+458G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123690 | ||||||
| chr9:104123975
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2257+743G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104123975 | ||||||
| chr9:104124093
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2258-819C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124093 | ||||||
| chr9:104124192
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2258-720G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124192 | ||||||
| chr9:104124279
|
GT | G | 14 | a0001c0001t0005g0007a0001c0001t0005g0026a0001c0001t0005g0027others(11): Show | 19 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.2258-629delT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 104124279 | |||||
| chr9:104124436
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2258-476C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124436 | ||||||
| chr9:104124437
|
A | G | 1 | a0001c0003t0004g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2258-475A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124437 | ||||||
| chr9:104124623
|
A | AT | 71 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(68): Show | 116 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2258-276dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 104124623 | |||||
| chr9:104124623
|
AT | A | 21 | a0001c0002t0001g0132a0001c0003t0004g0006a0001c0003t0004g0013others(18): Show | 29 | HG01169.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.2258-276delT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 104124623 | |||||
| chr9:104124636
|
T | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2258-276T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124636 | ||||||
| chr9:104124649
|
C | CAATACCT others(7): Show |
5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2258-261_2258-248d others(16): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 104124649 | |||||
| chr9:104124676
|
G | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2258-236G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124676 | ||||||
| chr9:104124747
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2258-165G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124747 | ||||||
| chr9:104124752
|
G | T | 1 | a0001c0001t0005g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2258-160G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124752 | ||||||
| chr9:104124800
|
A | G | 9 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(6): Show | 17 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.2258-112A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124800 | ||||||
| chr9:104124862
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2258-50C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 17/24 | chr9 | 104124862 | ||||||
| chr9:104125259
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2451+154T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125259 | ||||||
| chr9:104125289
|
A | G | 2 | a0005c0006t0012g0038a0005c0006t0012g0039 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2451+184A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125289 | ||||||
| chr9:104125295
|
A | T | 1 | a0004c0009t0001g0034 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2451+190A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125295 | ||||||
| chr9:104125300
|
A | G | 105 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(102): Show | 162 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.2451+195A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125300 | ||||||
| chr9:104125317
|
A | C | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.2451+212A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125317 | ||||||
| chr9:104125324
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2451+219A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125324 | ||||||
| chr9:104125431
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2451+326G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125431 | ||||||
| chr9:104125443
|
T | G | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2451+338T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125443 | ||||||
| chr9:104125636
|
A | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2451+531A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125636 | ||||||
| chr9:104125743
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2451+638T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125743 | ||||||
| chr9:104125763
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2451+658G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125763 | ||||||
| chr9:104125767
|
T | C | 1 | a0003c0004t0009g0024 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2451+662T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125767 | ||||||
| chr9:104125773
|
T | C | 1 | a0001c0010t0002g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2451+668T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125773 | ||||||
| chr9:104125871
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2451+766C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125871 | ||||||
| chr9:104125891
|
TC | T | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2452-749delC | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104125891 | ||||||
| chr9:104125949
|
AC | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2452-686delC | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr9 | 104125949 | |||||
| chr9:104126010
|
C | G | 2 | a0005c0006t0012g0038a0005c0006t0012g0039 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2452-631C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126010 | ||||||
| chr9:104126025
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2452-616T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126025 | ||||||
| chr9:104126180
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2452-461T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126180 | ||||||
| chr9:104126222
|
C | T | 1 | a0006c0012t0001g0160 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2452-419C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126222 | ||||||
| chr9:104126236
|
T | C | 19 | a0001c0001t0002g0029a0001c0001t0002g0089a0001c0001t0002g0090others(16): Show | 34 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.2452-405T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126236 | ||||||
| chr9:104126289
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2452-352G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126289 | ||||||
| chr9:104126314
|
T | C | 1 | a0001c0002t0006g0138 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2452-327T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126314 | ||||||
| chr9:104126368
|
A | G | 1 | a0001c0002t0001g0144 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2452-273A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126368 | ||||||
| chr9:104126369
|
T | A | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.2452-272T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126369 | ||||||
| chr9:104126373
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2452-268A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126373 | ||||||
| chr9:104126444
|
A | T | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2452-197A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126444 | ||||||
| chr9:104126447
|
C | CT | 23 | a0001c0001t0002g0074a0001c0001t0002g0085a0001c0003t0004g0006others(20): Show | 31 | HG01243.hp1 HG01891.hp2 HG02132.hp2 others(28): Show |
intron_variant | MODIFIER | c.2452-184dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr9 | 104126447 | |||||
| chr9:104126469
|
A | C | 61 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(58): Show | 105 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.2452-172A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126469 | ||||||
| chr9:104126478
|
C | CTTTTT | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2452-159_2452-158i others(7): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr9 | 104126478 | |||||
| chr9:104126541
|
T | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2452-100T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | chr9 | 104126541 | ||||||
| chr9:104126557
|
ATTAT | A | 80 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(77): Show | 129 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.2452-76_2452-73del others(4): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr9 | 104126557 | |||||
| chr9:104126806
|
C | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2595+22C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | chr9 | 104126806 | ||||||
| chr9:104126823
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2595+39G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | chr9 | 104126823 | ||||||
| chr9:104126835
|
G | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2595+51G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | chr9 | 104126835 | ||||||
| chr9:104126849
|
A | AGATGTTT others(21): Show |
1 | a0001c0003t0004g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2595+66_2595+93dup others(28): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr9 | 104126849 | |||||
| chr9:104126851
|
A | ATGTT | 5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595+70_2595+73dup others(4): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr9 | 104126851 | |||||
| chr9:104126985
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2595+201C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | chr9 | 104126985 | ||||||
| chr9:104127019
|
CA | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2595+241delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr9 | 104127019 | |||||
| chr9:104127096
|
A | G | 1 | a0001c0001t0016g0025 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2596-190A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | chr9 | 104127096 | ||||||
| chr9:104127192
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2596-94C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | chr9 | 104127192 | ||||||
| chr9:104127210
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2596-76T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | chr9 | 104127210 | ||||||
| chr9:104127223
|
T | C | 1 | a0001c0001t0002g0078 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2596-63T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 19/24 | chr9 | 104127223 | ||||||
| chr9:104127600
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2790+120G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104127600 | ||||||
| chr9:104127633
|
T | TCAACAAT others(10): Show |
1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2790+154_2790+170d others(19): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr9 | 104127633 | |||||
| chr9:104127939
|
T | C | 16 | a0001c0001t0001g0122a0001c0001t0005g0007a0001c0001t0005g0026others(13): Show | 21 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.2790+459T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104127939 | ||||||
| chr9:104128010
|
A | G | 1 | a0001c0002t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2790+530A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128010 | ||||||
| chr9:104128057
|
A | C | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2790+577A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128057 | ||||||
| chr9:104128253
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2790+773T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128253 | ||||||
| chr9:104128415
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2790+935C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128415 | ||||||
| chr9:104128492
|
T | G | 1 | a0001c0003t0004g0023 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2790+1012T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128492 | ||||||
| chr9:104128559
|
A | G | 82 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.2790+1079A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128559 | ||||||
| chr9:104128561
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2790+1081G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128561 | ||||||
| chr9:104128598
|
C | T | 1 | a0001c0008t0015g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2791-1047C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128598 | ||||||
| chr9:104128667
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2791-978T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104128667 | ||||||
| chr9:104129022
|
C | G | 1 | a0001c0001t0007g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2791-623C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129022 | ||||||
| chr9:104129135
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2791-510G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129135 | ||||||
| chr9:104129158
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2791-487T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129158 | ||||||
| chr9:104129221
|
G | C | 1 | a0001c0001t0002g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2791-424G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129221 | ||||||
| chr9:104129222
|
C | T | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2791-423C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129222 | ||||||
| chr9:104129240
|
C | T | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2791-405C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129240 | ||||||
| chr9:104129334
|
C | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2791-311C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129334 | ||||||
| chr9:104129518
|
A | AAATTAG | 20 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(17): Show | 28 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.2791-127_2791-126i others(8): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129518 | ||||||
| chr9:104129518
|
A | G | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2791-127A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129518 | ||||||
| chr9:104129520
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2791-125T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129520 | ||||||
| chr9:104129531
|
G | C | 1 | a0001c0002t0006g0139 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2791-114G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 20/24 | chr9 | 104129531 | ||||||
| chr9:104129899
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2991+54C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104129899 | ||||||
| chr9:104129998
|
TTTC | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0073 | 4 | HG01069.hp2 HG01071.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.2991+156_2991+158d others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr9 | 104129998 | |||||
| chr9:104130129
|
T | C | 5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2991+284T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104130129 | ||||||
| chr9:104130302
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2991+457T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104130302 | ||||||
| chr9:104130544
|
C | T | 1 | a0001c0002t0011g0137 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2991+699C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104130544 | ||||||
| chr9:104130586
|
TA | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2991+743delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr9 | 104130586 | |||||
| chr9:104130589
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2991+744T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104130589 | ||||||
| chr9:104130758
|
T | C | 2 | a0001c0008t0015g0113a0001c0008t0015g0114 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2991+913T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104130758 | ||||||
| chr9:104130922
|
T | C | 1 | a0001c0002t0001g0146 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2991+1077T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104130922 | ||||||
| chr9:104130980
|
A | G | 1 | a0001c0002t0001g0136 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2992-1029A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104130980 | ||||||
| chr9:104130996
|
A | G | 4 | a0001c0002t0001g0132a0001c0002t0001g0135a0001c0002t0001g0164others(1): Show | 4 | HG01169.hp2 HG01978.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.2992-1013A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104130996 | ||||||
| chr9:104131053
|
A | G | 105 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(102): Show | 162 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.2992-956A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131053 | ||||||
| chr9:104131057
|
G | A | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2992-952G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131057 | ||||||
| chr9:104131141
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2992-868T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131141 | ||||||
| chr9:104131197
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2992-812A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131197 | ||||||
| chr9:104131233
|
G | A | 1 | a0001c0007t0001g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2992-776G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131233 | ||||||
| chr9:104131258
|
G | A | 1 | a0001c0008t0015g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2992-751G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131258 | ||||||
| chr9:104131433
|
T | G | 2 | a0001c0008t0015g0113a0001c0008t0015g0114 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2992-576T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131433 | ||||||
| chr9:104131447
|
A | G | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2992-562A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131447 | ||||||
| chr9:104131514
|
T | TA | 3 | a0001c0001t0002g0003a0001c0001t0002g0082a0001c0001t0034g0003 | 10 | HG01074.hp1 HG01975.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2992-487dupA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr9 | 104131514 | |||||
| chr9:104131650
|
C | CT | 46 | a0001c0001t0002g0008a0001c0001t0002g0016a0001c0001t0002g0017others(43): Show | 72 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.2992-342dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr9 | 104131650 | |||||
| chr9:104131650
|
C | CTT | 35 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(32): Show | 59 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2992-343_2992-342d others(4): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr9 | 104131650 | |||||
| chr9:104131650
|
CT | C | 13 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(10): Show | 21 | HG02132.hp2 HG02280.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.2992-342delT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr9 | 104131650 | |||||
| chr9:104131707
|
CA | C | 5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2992-298delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr9 | 104131707 | |||||
| chr9:104131752
|
A | G | 1 | a0001c0002t0006g0143 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2992-257A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131752 | ||||||
| chr9:104131807
|
A | G | 1 | a0001c0001t0016g0025 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2992-202A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131807 | ||||||
| chr9:104131930
|
A | C | 82 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.2992-79A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131930 | ||||||
| chr9:104131930
|
A | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2992-79A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131930 | ||||||
| chr9:104131976
|
T | G | 20 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(17): Show | 28 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.2992-33T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 21/24 | chr9 | 104131976 | ||||||
| chr9:104132198
|
G | A | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3108+73G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104132198 | ||||||
| chr9:104132210
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3108+85A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104132210 | ||||||
| chr9:104132276
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3108+151T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104132276 | ||||||
| chr9:104132295
|
G | T | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3108+170G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104132295 | ||||||
| chr9:104132492
|
A | G | 1 | a0001c0011t0005g0062 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3108+367A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104132492 | ||||||
| chr9:104132539
|
C | T | 1 | a0001c0002t0001g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3108+414C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104132539 | ||||||
| chr9:104132840
|
G | GT | 17 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(14): Show | 25 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.3108+728dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr9 | 104132840 | |||||
| chr9:104132840
|
G | GTT | 6 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(3): Show | 6 | HG02132.hp2 HG03453.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+727_3108+728d others(4): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr9 | 104132840 | |||||
| chr9:104132874
|
G | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3108+749G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104132874 | ||||||
| chr9:104133121
|
C | CT | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3108+1003dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr9 | 104133121 | |||||
| chr9:104133196
|
C | T | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3108+1071C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133196 | ||||||
| chr9:104133197
|
G | A | 1 | a0001c0001t0030g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3108+1072G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133197 | ||||||
| chr9:104133322
|
C | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3109-1093C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133322 | ||||||
| chr9:104133364
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3109-1051T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133364 | ||||||
| chr9:104133411
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3109-1004G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133411 | ||||||
| chr9:104133444
|
T | C | 1 | a0001c0001t0029g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3109-971T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133444 | ||||||
| chr9:104133573
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3109-842A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133573 | ||||||
| chr9:104133695
|
A | G | 1 | a0001c0001t0036g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3109-720A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133695 | ||||||
| chr9:104133830
|
C | T | 64 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(61): Show | 108 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.3109-585C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133830 | ||||||
| chr9:104133950
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3109-465T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104133950 | ||||||
| chr9:104134026
|
A | G | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-389A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104134026 | ||||||
| chr9:104134070
|
G | A | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(18): Show | 39 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.3109-345G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104134070 | ||||||
| chr9:104134206
|
A | G | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-209A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104134206 | ||||||
| chr9:104134222
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3109-193T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104134222 | ||||||
| chr9:104134382
|
T | A | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-33T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 22/24 | chr9 | 104134382 | ||||||
| chr9:104134593
|
T | TATATTAT others(2): Show |
106 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(103): Show | 164 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.3269+19_3269+27dup others(9): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104134593 | |||||
| chr9:104134602
|
A | AATATTAT others(3): Show |
1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3269+27_3269+28ins others(10): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104134602 | ||||||
| chr9:104134672
|
A | G | 1 | a0001c0003t0013g0048 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3269+97A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104134672 | ||||||
| chr9:104134689
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3269+114T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104134689 | ||||||
| chr9:104134742
|
C | G | 1 | a0001c0001t0003g0093 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3269+167C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104134742 | ||||||
| chr9:104134828
|
A | G | 1 | a0001c0008t0015g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3269+253A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104134828 | ||||||
| chr9:104134877
|
C | G | 1 | a0001c0001t0036g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3269+302C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104134877 | ||||||
| chr9:104134995
|
A | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3269+420A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104134995 | ||||||
| chr9:104135071
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3269+496T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135071 | ||||||
| chr9:104135210
|
C | CAGATGAT others(11): Show |
86 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.3269+637_3269+654d others(20): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104135210 | |||||
| chr9:104135210
|
C | CAGATGAT others(11): Show |
21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3269+643_3269+644i others(20): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104135210 | |||||
| chr9:104135255
|
A | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3269+680A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135255 | ||||||
| chr9:104135299
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3269+724T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135299 | ||||||
| chr9:104135336
|
T | G | 1 | a0001c0002t0001g0140 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3269+761T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135336 | ||||||
| chr9:104135425
|
AAACTGG | A | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3269+852_3269+857d others(8): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104135425 | |||||
| chr9:104135472
|
T | C | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.3269+897T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135472 | ||||||
| chr9:104135504
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3269+929A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135504 | ||||||
| chr9:104135526
|
C | T | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3269+951C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135526 | ||||||
| chr9:104135772
|
G | A | 1 | a0001c0001t0030g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3269+1197G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135772 | ||||||
| chr9:104135854
|
T | C | 2 | a0005c0006t0012g0038a0005c0006t0012g0039 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3269+1279T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104135854 | ||||||
| chr9:104136013
|
C | T | 2 | a0001c0008t0015g0113a0001c0008t0015g0114 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3269+1438C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136013 | ||||||
| chr9:104136092
|
G | T | 1 | a0003c0004t0009g0024 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3269+1517G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136092 | ||||||
| chr9:104136126
|
C | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3269+1551C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136126 | ||||||
| chr9:104136129
|
C | T | 106 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(103): Show | 164 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.3269+1554C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136129 | ||||||
| chr9:104136296
|
C | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3269+1721C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136296 | ||||||
| chr9:104136304
|
C | G | 1 | a0001c0002t0001g0155 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3270-1714C>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136304 | ||||||
| chr9:104136383
|
C | T | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3270-1635C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136383 | ||||||
| chr9:104136495
|
C | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-1523C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136495 | ||||||
| chr9:104136517
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-1501A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136517 | ||||||
| chr9:104136528
|
G | T | 1 | a0001c0002t0001g0135 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3270-1490G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136528 | ||||||
| chr9:104136529
|
C | T | 1 | a0001c0002t0001g0135 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3270-1489C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136529 | ||||||
| chr9:104136568
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-1450T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136568 | ||||||
| chr9:104136628
|
C | T | 5 | a0001c0003t0008g0043a0001c0003t0008g0044a0001c0003t0008g0045others(2): Show | 5 | HG02132.hp2 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.3270-1390C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136628 | ||||||
| chr9:104136636
|
A | G | 5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3270-1382A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136636 | ||||||
| chr9:104136686
|
GT | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-1329delT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104136686 | |||||
| chr9:104136755
|
C | CT | 6 | a0001c0001t0002g0111a0001c0001t0030g0091a0001c0002t0001g0033others(3): Show | 7 | HG01981.hp2 HG02055.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.3270-1246dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104136755 | |||||
| chr9:104136755
|
C | CTTTT | 14 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(11): Show | 22 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.3270-1249_3270-124 others(8): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104136755 | |||||
| chr9:104136755
|
CTTTTTTT | C | 5 | a0001c0003t0013g0048a0001c0003t0013g0050a0001c0003t0017g0049others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3270-1252_3270-124 others(11): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104136755 | |||||
| chr9:104136774
|
G | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-1244G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136774 | ||||||
| chr9:104136781
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3270-1237A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136781 | ||||||
| chr9:104136899
|
G | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-1119G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136899 | ||||||
| chr9:104136916
|
A | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-1102A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136916 | ||||||
| chr9:104136977
|
G | A | 2 | a0001c0007t0001g0041a0001c0007t0001g0042 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3270-1041G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104136977 | ||||||
| chr9:104137085
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-933T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137085 | ||||||
| chr9:104137319
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-699G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137319 | ||||||
| chr9:104137560
|
A | ATATGCAT others(20): Show |
1 | a0001c0003t0004g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3270-437_3270-436i others(29): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104137560 | |||||
| chr9:104137582
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-436T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137582 | ||||||
| chr9:104137644
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-374T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137644 | ||||||
| chr9:104137670
|
TA | T | 106 | a0001c0001t0001g0122a0001c0001t0002g0002a0001c0001t0002g0003others(103): Show | 164 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.3270-346delA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104137670 | |||||
| chr9:104137720
|
G | A | 2 | a0001c0008t0015g0113a0001c0008t0015g0114 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3270-298G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137720 | ||||||
| chr9:104137811
|
AGAG | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-203_3270-201d others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104137811 | |||||
| chr9:104137843
|
T | TATATAAA others(3): Show |
21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-174_3270-173i others(12): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104137843 | |||||
| chr9:104137855
|
A | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-163A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137855 | ||||||
| chr9:104137856
|
C | A | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-162C>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137856 | ||||||
| chr9:104137858
|
A | AGTT | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-160_3270-159i others(5): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137858 | ||||||
| chr9:104137859
|
C | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-159C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137859 | ||||||
| chr9:104137862
|
A | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-156A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137862 | ||||||
| chr9:104137863
|
A | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-155A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137863 | ||||||
| chr9:104137864
|
G | T | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-154G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137864 | ||||||
| chr9:104137865
|
T | A | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-153T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137865 | ||||||
| chr9:104137866
|
G | A | 10 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(7): Show | 18 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.3270-152G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137866 | ||||||
| chr9:104137889
|
C | CT | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3270-121dupT | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr9 | 104137889 | |||||
| chr9:104137923
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3270-95G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137923 | ||||||
| chr9:104137980
|
A | C | 2 | a0001c0001t0002g0077a0001c0001t0002g0092 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3270-38A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 23/24 | chr9 | 104137980 | ||||||
| chr9:104138177
|
G | GA | 3 | a0003c0004t0009g0024a0003c0004t0009g0040a0003c0004t0025g0072 | 4 | HG02809.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3417+19dupA | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr9 | 104138177 | |||||
| chr9:104138215
|
T | C | 1 | a0001c0003t0027g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3417+50T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138215 | ||||||
| chr9:104138251
|
A | C | 1 | a0001c0002t0001g0156 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3417+86A>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138251 | ||||||
| chr9:104138311
|
T | G | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3417+146T>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138311 | ||||||
| chr9:104138366
|
A | G | 1 | a0003c0004t0009g0024 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3417+201A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138366 | ||||||
| chr9:104138496
|
G | A | 1 | a0001c0001t0031g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3417+331G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138496 | ||||||
| chr9:104138509
|
G | C | 20 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(17): Show | 28 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3417+344G>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138509 | ||||||
| chr9:104138524
|
C | T | 20 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(17): Show | 28 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.3417+359C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138524 | ||||||
| chr9:104138574
|
CAAAG | C | 22 | a0001c0001t0002g0103a0001c0003t0004g0006a0001c0003t0004g0013others(19): Show | 30 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.3417+414_3417+417d others(6): Show |
SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr9 | 104138574 | |||||
| chr9:104138667
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3418-472A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138667 | ||||||
| chr9:104138740
|
A | G | 1 | a0001c0001t0036g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3418-399A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138740 | ||||||
| chr9:104138754
|
C | T | 15 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(12): Show | 23 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(20): Show |
intron_variant | MODIFIER | c.3418-385C>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138754 | ||||||
| chr9:104138758
|
G | A | 6 | a0001c0002t0001g0020a0001c0002t0001g0032a0001c0002t0001g0125others(3): Show | 8 | HG00280.hp1 HG01069.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.3418-381G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138758 | ||||||
| chr9:104138891
|
A | T | 1 | a0001c0001t0003g0095 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3418-248A>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138891 | ||||||
| chr9:104138948
|
G | T | 4 | a0001c0002t0001g0021a0001c0002t0001g0149a0001c0002t0001g0151others(1): Show | 6 | HG00438.hp1 HG00558.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.3418-191G>T | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138948 | ||||||
| chr9:104138952
|
T | A | 2 | a0005c0006t0012g0038a0005c0006t0012g0039 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3418-187T>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138952 | ||||||
| chr9:104138953
|
G | A | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3418-186G>A | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138953 | ||||||
| chr9:104138957
|
T | C | 21 | a0001c0003t0004g0006a0001c0003t0004g0013a0001c0003t0004g0022others(18): Show | 29 | HG01891.hp2 HG02132.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3418-182T>C | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104138957 | ||||||
| chr9:104139059
|
A | G | 1 | a0001c0001t0003g0058 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3418-80A>G | SMC2 | ENSG00000136824.19 | transcript | ENST00000374793.8 | protein_coding | 24/24 | chr9 | 104139059 |