| geneid | 23137 |
|---|---|
| ensemblid | ENSG00000198887.9 |
| hgncid | 20465 |
| symbol | SMC5 |
| name | structural maintenance of chromosomes 5 |
| refseq_nuc | NM_015110.4 |
| refseq_prot | NP_055925.2 |
| ensembl_nuc | ENST00000361138.7 |
| ensembl_prot | ENSP00000354957.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 70258978 |
| end | 70354873 |
| strand | + |
| ver | v1.2 |
| region | chr9:70258978-70354873 |
| region5000 | chr9:70253978-70359873 |
| regionname0 | SMC5_chr9_70258978_70354873 |
| regionname5000 | SMC5_chr9_70253978_70359873 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1101 | 158 | 38 | 40 | 64 | 4 | 12 | 45 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002 | 0/0 | 1101 | 90 | 6 | 11 | 56 | 1 | 16 | 47 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0003 | 1/1 | 1101 | 68 | 20 | 8 | 29 | 3 | 6 | 21 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0004 | 0/0 | 1101 | 31 | 15 | 10 | 2 | 2 | 2 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0005 | 0/0 | 1101 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0006 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0007 | 0/0 | 1101 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0008 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0009 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0010 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0011 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0012 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0013 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0014 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0015 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0016 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3306 | 148 | 32 | 39 | 61 | 4 | 12 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0002 | 0/0 | 3306 | 86 | 2 | 11 | 56 | 1 | 16 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0003 | 1/1 | 3306 | 68 | 20 | 8 | 29 | 3 | 6 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0004 | 0/0 | 3306 | 20 | 7 | 8 | 2 | 1 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0005 | 0/0 | 3306 | 7 | 6 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0006 | 0/0 | 3306 | 6 | 6 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0007 | 0/0 | 3306 | 6 | 5 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0008 | 0/0 | 3306 | 5 | 2 | 2 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0009 | 0/0 | 3306 | 3 | 3 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0010 | 0/0 | 3306 | 3 | 0 | 0 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0011 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0012 | 0/0 | 3306 | 2 | 0 | 0 | 0 | 0 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0013 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0014 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0015 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0016 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0017 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0018 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0019 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0020 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0021 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| c0022 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2644 | 169 | 32 | 21 | 84 | 4 | 26 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0002 | 0/0 | 2644 | 151 | 35 | 37 | 64 | 4 | 11 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0003 | 0/0 | 2643 | 8 | 7 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0004 | 0/0 | 2644 | 7 | 0 | 5 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0005 | 0/0 | 2644 | 5 | 2 | 2 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0006 | 0/0 | 2644 | 4 | 4 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0007 | 0/0 | 2644 | 3 | 1 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0008 | 0/0 | 2644 | 3 | 1 | 1 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0009 | 0/0 | 2644 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0010 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0011 | 0/0 | 2644 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0012 | 0/0 | 2644 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0013 | 0/0 | 2644 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0014 | 0/0 | 2644 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0015 | 0/0 | 2644 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0016 | 0/0 | 2644 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0017 | 0/0 | 2644 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0018 | 0/0 | 2644 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0019 | 0/0 | 2644 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0020 | 0/0 | 2644 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0021 | 0/0 | 2644 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0022 | 0/0 | 2644 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| t0023 | 0/0 | 2644 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3306 | 148 | 32 | 39 | 61 | 4 | 12 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0005 | 0/0 | 3306 | 7 | 6 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0010 | 0/0 | 3306 | 3 | 0 | 0 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0002 | 0/0 | 3306 | 86 | 2 | 11 | 56 | 1 | 16 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0009 | 0/0 | 3306 | 3 | 3 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0013 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0003c0003 | 1/1 | 3306 | 68 | 20 | 8 | 29 | 3 | 6 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0004c0004 | 0/0 | 3306 | 20 | 7 | 8 | 2 | 1 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0004c0006 | 0/0 | 3306 | 6 | 6 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0004c0008 | 0/0 | 3306 | 5 | 2 | 2 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0005c0007 | 0/0 | 3306 | 6 | 5 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0006c0011 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0007c0012 | 0/0 | 3306 | 2 | 0 | 0 | 0 | 0 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0008c0021 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0009c0019 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0010c0016 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0011c0017 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0012c0014 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0013c0015 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0014c0018 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0015c0020 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0016c0022 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5949 | 140 | 30 | 36 | 59 | 4 | 11 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0001t0007 | 0/0 | 5949 | 3 | 1 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0001t0015 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0001t0016 | 0/0 | 5949 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0001t0017 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0001t0021 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0001t0023 | 0/0 | 5949 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0005t0003 | 0/0 | 5948 | 7 | 6 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0001c0010t0002 | 0/0 | 5949 | 3 | 0 | 0 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0002t0001 | 0/0 | 5949 | 75 | 1 | 6 | 51 | 1 | 16 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0002t0004 | 0/0 | 5949 | 7 | 0 | 5 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0002t0010 | 0/0 | 5973 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0002t0013 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0002t0019 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0002t0022 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0009t0006 | 0/0 | 5949 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0009t0014 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0002c0013t0006 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0003c0003t0001 | 1/1 | 5949 | 64 | 19 | 7 | 28 | 2 | 6 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0003c0003t0008 | 0/0 | 5949 | 3 | 1 | 1 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0003c0003t0020 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0004c0004t0001 | 0/0 | 5949 | 19 | 6 | 8 | 2 | 1 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0004c0004t0018 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0004c0006t0001 | 0/0 | 5949 | 6 | 6 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0004c0008t0005 | 0/0 | 5949 | 5 | 2 | 2 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0005c0007t0002 | 0/0 | 5949 | 6 | 5 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0006c0011t0009 | 0/0 | 5949 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0007c0012t0001 | 0/0 | 5949 | 2 | 0 | 0 | 0 | 0 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0008c0021t0001 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0009c0019t0003 | 0/0 | 5948 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0010c0016t0002 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0011c0017t0002 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0012c0014t0001 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0013c0015t0011 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0014c0018t0001 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0015c0020t0006 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| a0016c0022t0012 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | copy fasta | chr9 | 70253978 | 70359873 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0007g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0007g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0015g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0016g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0017g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0021g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0001t0023g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0005t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0005t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0005t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0005t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0005t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0005t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0005t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0010t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0010t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0001c0010t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0004g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0013g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0019g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0002t0022g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0009t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0009t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0009t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0002c0013t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0008g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0008g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0003c0003t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0004t0018g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0006t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0006t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0006t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0006t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0006t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0006t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0008t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0008t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0008t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0008t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0004c0008t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0005c0007t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0005c0007t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0005c0007t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0005c0007t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0005c0007t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0006c0011t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0006c0011t0009g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0007c0012t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0007c0012t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0008c0021t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0009c0019t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0010c0016t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0011c0017t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0012c0014t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0013c0015t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0014c0018t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0015c0020t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| a0016c0022t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0174 | EUR | GBR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | GBR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0298 | EUR | GBR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00140 | hp2 | a0004 | c0004 | t0001 | g0341 | EUR | GBR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0177 | EUR | FIN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0134 | EUR | FIN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00597 | hp2 | a0012 | c0014 | t0001 | g0065 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0190 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0318 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0291 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00738 | hp2 | a0004 | c0008 | t0005 | g0101 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0293 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01070 | hp2 | a0004 | c0004 | t0001 | g0329 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01071 | hp2 | a0004 | c0004 | t0001 | g0330 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0176 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01099 | hp1 | a0004 | c0004 | t0001 | g0321 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01106 | hp1 | a0003 | c0003 | t0008 | g0200 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01106 | hp2 | a0004 | c0004 | t0001 | g0339 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0147 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0172 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01255 | hp2 | a0004 | c0004 | t0001 | g0326 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01256 | hp2 | a0004 | c0004 | t0001 | g0323 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01258 | hp2 | a0004 | c0004 | t0001 | g0322 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01346 | hp1 | a0004 | c0004 | t0001 | g0325 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01358 | hp2 | a0005 | c0007 | t0002 | g0281 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0160 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01433 | hp1 | a0004 | c0008 | t0005 | g0102 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01496 | hp1 | a0001 | c0005 | t0003 | g0024 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0201 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01884 | hp2 | a0013 | c0015 | t0011 | g0108 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01891 | hp2 | a0002 | c0009 | t0006 | g0095 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01943 | hp1 | a0002 | c0002 | t0004 | g0085 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01975 | hp2 | a0002 | c0002 | t0004 | g0086 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0165 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG01993 | hp2 | a0002 | c0002 | t0004 | g0007 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02040 | hp2 | a0001 | c0010 | t0002 | g0016 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02055 | hp2 | a0004 | c0006 | t0001 | g0332 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02071 | hp1 | a0001 | c0001 | t0017 | g0218 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02071 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02080 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02083 | hp1 | a0003 | c0003 | t0001 | g0192 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0197 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02135 | hp1 | a0001 | c0010 | t0002 | g0278 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02145 | hp1 | a0003 | c0003 | t0008 | g0198 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0191 | EAS | CDX | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | CDX | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02165 | hp1 | a0003 | c0003 | t0020 | g0194 | EAS | CDX | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CDX | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02257 | hp1 | a0001 | c0001 | t0021 | g0317 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02257 | hp2 | a0004 | c0006 | t0001 | g0340 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0309 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02273 | hp2 | a0002 | c0002 | t0004 | g0084 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0146 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02280 | hp2 | a0004 | c0004 | t0001 | g0344 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02293 | hp1 | a0001 | c0001 | t0023 | g0252 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02293 | hp2 | a0002 | c0002 | t0004 | g0087 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0153 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02451 | hp1 | a0001 | c0005 | t0003 | g0023 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02451 | hp2 | a0016 | c0022 | t0012 | g0149 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02523 | hp1 | a0008 | c0021 | t0001 | g0064 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02572 | hp1 | a0001 | c0005 | t0003 | g0019 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02572 | hp2 | a0001 | c0005 | t0003 | g0022 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0312 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02615 | hp2 | a0002 | c0009 | t0014 | g0097 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0314 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02630 | hp2 | a0005 | c0007 | t0002 | g0015 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0346 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02717 | hp2 | a0004 | c0006 | t0001 | g0331 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0168 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0145 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02738 | hp2 | a0001 | c0001 | t0016 | g0297 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02809 | hp1 | a0004 | c0008 | t0005 | g0103 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02809 | hp2 | a0004 | c0006 | t0001 | g0342 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0009 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02818 | hp2 | a0004 | c0006 | t0001 | g0333 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0173 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02895 | hp1 | a0006 | c0011 | t0009 | g0310 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02895 | hp2 | a0004 | c0004 | t0001 | g0334 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02897 | hp1 | a0006 | c0011 | t0009 | g0311 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02965 | hp1 | a0001 | c0005 | t0003 | g0021 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02970 | hp1 | a0015 | c0020 | t0006 | g0096 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02976 | hp1 | a0004 | c0004 | t0001 | g0338 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03041 | hp1 | a0001 | c0005 | t0003 | g0020 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03130 | hp1 | a0005 | c0007 | t0002 | g0015 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0170 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03209 | hp2 | a0002 | c0013 | t0006 | g0099 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03225 | hp1 | a0002 | c0009 | t0006 | g0098 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03453 | hp1 | a0004 | c0008 | t0005 | g0100 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0080 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0290 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03486 | hp2 | a0004 | c0004 | t0001 | g0337 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0091 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03516 | hp1 | a0004 | c0004 | t0001 | g0320 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03516 | hp2 | a0009 | c0019 | t0003 | g0017 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03540 | hp2 | a0005 | c0007 | t0002 | g0280 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0106 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0202 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0090 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0328 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0152 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03669 | hp2 | a0007 | c0012 | t0001 | g0179 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03831 | hp1 | a0007 | c0012 | t0001 | g0107 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0154 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0058 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0119 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG04115 | hp2 | a0004 | c0004 | t0001 | g0327 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0155 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0035 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0044 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0180 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0003 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18522 | hp2 | a0005 | c0007 | t0002 | g0279 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | CHB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18747 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | CHB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0148 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18945 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18947 | hp2 | a0002 | c0002 | t0004 | g0094 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18949 | hp2 | a0002 | c0002 | t0010 | g0055 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18953 | hp2 | a0001 | c0010 | t0002 | g0263 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18969 | hp1 | a0014 | c0018 | t0001 | g0196 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18986 | hp1 | a0002 | c0002 | t0019 | g0045 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18986 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18987 | hp2 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0189 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18999 | hp2 | a0004 | c0004 | t0001 | g0324 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0188 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19010 | hp1 | a0001 | c0001 | t0015 | g0266 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19011 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0150 | AFR | LWK | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | LWK | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0171 | AFR | LWK | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19043 | hp2 | a0004 | c0004 | t0018 | g0345 | AFR | LWK | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19055 | hp1 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19057 | hp1 | a0011 | c0017 | t0002 | g0214 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19058 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19078 | hp2 | a0002 | c0002 | t0022 | g0074 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19080 | hp2 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19081 | hp1 | a0010 | c0016 | t0002 | g0301 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19084 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19240 | hp1 | a0001 | c0005 | t0003 | g0018 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA19240 | hp2 | a0004 | c0004 | t0001 | g0335 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ASW | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA20129 | hp2 | a0002 | c0002 | t0013 | g0319 | AFR | ASW | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0235 | EUR | TSI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA20752 | hp2 | a0004 | c0008 | t0005 | g0104 | EUR | TSI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA20805 | hp1 | a0003 | c0003 | t0008 | g0175 | EUR | TSI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0169 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02109 | hp2 | a0004 | c0006 | t0001 | g0336 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03471 | hp1 | a0005 | c0007 | t0002 | g0282 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | USA | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | USA | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA18955 | hp2 | a0004 | c0004 | t0001 | g0343 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | USA | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | USA | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0199 | REF | REF | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0167 | REF | REF | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:70264314
|
A | G | 1 | a0016 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.196A>G | p.Ile66Val | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/25 | 297/5949 | 196/3306 | 66/1101 | chr9 | 70264314 | ||
| chr9:70264329
|
C | G | 1 | a0008 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.211C>G | p.Pro71Ala | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/25 | 312/5949 | 211/3306 | 71/1101 | chr9 | 70264329 | ||
| chr9:70277425
|
G | T | 1 | a0015 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.496G>T | p.Ala166Ser | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/25 | 597/5949 | 496/3306 | 166/1101 | chr9 | 70277425 | ||
| chr9:70277458
|
C | G | 1 | a0009 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.529C>G | p.Gln177Glu | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/25 | 630/5949 | 529/3306 | 177/1101 | chr9 | 70277458 | ||
| chr9:70282518
|
G | A | 12 | a0001a0002a0004others(9): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
missense_variant | MODERATE | c.916G>A | p.Val306Ile | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/25 | 1017/5949 | 916/3306 | 306/1101 | chr9 | 70282518 | ||
| chr9:70282524
|
T | C | 7 | a0002a0004a0006others(4): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
missense_variant | MODERATE | c.922T>C | p.Cys308Arg | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/25 | 1023/5949 | 922/3306 | 308/1101 | chr9 | 70282524 | ||
| chr9:70298125
|
A | G | 1 | a0006 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1213A>G | p.Asn405Asp | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/25 | 1314/5949 | 1213/3306 | 405/1101 | chr9 | 70298125 | ||
| chr9:70298137
|
C | T | 1 | a0011 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1225C>T | p.Arg409Trp | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/25 | 1326/5949 | 1225/3306 | 409/1101 | chr9 | 70298137 | ||
| chr9:70318858
|
A | G | 2 | a0004a0013 | 32 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(29): Show |
missense_variant | MODERATE | c.2045A>G | p.His682Arg | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/25 | 2146/5949 | 2045/3306 | 682/1101 | chr9 | 70318858 | ||
| chr9:70323530
|
G | A | 1 | a0005 | 6 | HG01358.hp2 HG02630.hp2 HG03130.hp1 others(3): Show |
missense_variant | MODERATE | c.2198G>A | p.Arg733Gln | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 16/25 | 2299/5949 | 2198/3306 | 733/1101 | chr9 | 70323530 | ||
| chr9:70324117
|
G | A | 1 | a0013 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.2371G>A | p.Ala791Thr | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/25 | 2472/5949 | 2371/3306 | 791/1101 | chr9 | 70324117 | ||
| chr9:70347640
|
G | A | 1 | a0014 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2692G>A | p.Glu898Lys | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 21/25 | 2793/5949 | 2692/3306 | 898/1101 | chr9 | 70347640 | ||
| chr9:70347983
|
A | G | 1 | a0010 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.2834A>G | p.Asn945Ser | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/25 | 2935/5949 | 2834/3306 | 945/1101 | chr9 | 70347983 | ||
| chr9:70350160
|
G | A | 1 | a0007 | 2 | HG03669.hp2 HG03831.hp1 |
missense_variant | MODERATE | c.2936G>A | p.Ser979Asn | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 23/25 | 3037/5949 | 2936/3306 | 979/1101 | chr9 | 70350160 | ||
| chr9:70352303
|
G | A | 1 | a0012 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.3278G>A | p.Arg1093His | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 3379/5949 | 3278/3306 | 1093/1101 | chr9 | 70352303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:70264388
|
G | A | 1 | a0004c0006 | 6 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
synonymous_variant | LOW | c.270G>A | p.Val90Val | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/25 | 371/5949 | 270/3306 | 90/1101 | chr9 | 70264388 | ||
| chr9:70282547
|
C | T | 1 | a0001c0010 | 3 | HG02040.hp2 HG02135.hp1 NA18953.hp2 |
synonymous_variant | LOW | c.945C>T | p.Asn315Asn | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/25 | 1046/5949 | 945/3306 | 315/1101 | chr9 | 70282547 | ||
| chr9:70297998
|
G | A | 1 | a0004c0008 | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1086G>A | p.Lys362Lys | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/25 | 1187/5949 | 1086/3306 | 362/1101 | chr9 | 70297998 | ||
| chr9:70300125
|
G | A | 1 | a0002c0013 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1389G>A | p.Thr463Thr | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/25 | 1490/5949 | 1389/3306 | 463/1101 | chr9 | 70300125 | ||
| chr9:70318682
|
C | T | 2 | a0001c0005a0009c0019 | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.1975C>T | p.Leu659Leu | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 14/25 | 2076/5949 | 1975/3306 | 659/1101 | chr9 | 70318682 | ||
| chr9:70318889
|
A | G | 3 | a0002c0009a0002c0013a0015c0020 | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.2076A>G | p.Gln692Gln | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/25 | 2177/5949 | 2076/3306 | 692/1101 | chr9 | 70318889 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:70258992
|
C | CGGGGCGC others(17): Show |
1 | a0002c0002t0010 | 1 | NA18949.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86_-63dupGGGGCGCC others(16): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/25 | 62 | INFO_REALIGN_3_PRIME | chr9 | 70258992 | ||||
| chr9:70259022
|
G | C | 1 | a0013c0015t0011 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/25 | 57 | chr9 | 70259022 | |||||
| chr9:70352358
|
A | T | 1 | a0006c0011t0009 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*27A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 27 | chr9 | 70352358 | |||||
| chr9:70352514
|
A | G | 1 | a0001c0001t0023 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 183 | chr9 | 70352514 | |||||
| chr9:70352541
|
G | A | 1 | a0016c0022t0012 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 210 | chr9 | 70352541 | |||||
| chr9:70352656
|
T | C | 1 | a0002c0002t0013 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 325 | chr9 | 70352656 | |||||
| chr9:70352808
|
C | T | 1 | a0002c0002t0022 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 477 | chr9 | 70352808 | |||||
| chr9:70352978
|
AT | A | 2 | a0001c0005t0003a0009c0019t0003 | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*648delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 648 | chr9 | 70352978 | |||||
| chr9:70353052
|
G | A | 4 | a0002c0009t0006a0002c0009t0014a0002c0013t0006others(1): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*721G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 721 | chr9 | 70353052 | |||||
| chr9:70353122
|
A | G | 1 | a0004c0008t0005 | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*791A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 791 | chr9 | 70353122 | |||||
| chr9:70353240
|
G | A | 1 | a0013c0015t0011 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 909 | chr9 | 70353240 | |||||
| chr9:70353271
|
C | A | 1 | a0001c0001t0023 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 940 | chr9 | 70353271 | |||||
| chr9:70353297
|
A | G | 1 | a0001c0001t0021 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*966A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 966 | chr9 | 70353297 | |||||
| chr9:70353646
|
G | A | 1 | a0006c0011t0009 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1315G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1315 | chr9 | 70353646 | |||||
| chr9:70353714
|
T | G | 2 | a0001c0005t0003a0009c0019t0003 | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1383T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1383 | chr9 | 70353714 | |||||
| chr9:70353824
|
G | A | 1 | a0001c0001t0015 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1493G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1493 | chr9 | 70353824 | |||||
| chr9:70353878
|
G | A | 1 | a0001c0001t0016 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1547 | chr9 | 70353878 | |||||
| chr9:70353988
|
G | C | 1 | a0001c0001t0017 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1657G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1657 | chr9 | 70353988 | |||||
| chr9:70354240
|
T | G | 1 | a0001c0001t0021 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1909T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1909 | chr9 | 70354240 | |||||
| chr9:70354386
|
C | G | 1 | a0003c0003t0020 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2055C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2055 | chr9 | 70354386 | |||||
| chr9:70354472
|
G | A | 2 | a0001c0001t0007a0002c0009t0014 | 4 | HG00738.hp1 HG01070.hp1 HG02615.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2141G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2141 | chr9 | 70354472 | |||||
| chr9:70354477
|
G | A | 1 | a0004c0004t0018 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2146G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2146 | chr9 | 70354477 | |||||
| chr9:70354505
|
G | A | 1 | a0006c0011t0009 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2174G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2174 | chr9 | 70354505 | |||||
| chr9:70354517
|
A | G | 1 | a0006c0011t0009 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2186A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2186 | chr9 | 70354517 | |||||
| chr9:70354553
|
C | T | 1 | a0002c0002t0004 | 7 | HG01943.hp1 HG01975.hp2 HG01993.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2222C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2222 | chr9 | 70354553 | |||||
| chr9:70354601
|
A | T | 11 | a0001c0001t0002a0001c0001t0007a0001c0001t0015others(8): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2270A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2270 | chr9 | 70354601 | |||||
| chr9:70354629
|
A | C | 1 | a0004c0008t0005 | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2298A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2298 | chr9 | 70354629 | |||||
| chr9:70354738
|
C | T | 1 | a0003c0003t0008 | 3 | HG01106.hp1 HG02145.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2407C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2407 | chr9 | 70354738 | |||||
| chr9:70354761
|
C | G | 1 | a0002c0002t0019 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2430 | chr9 | 70354761 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:70259267
|
A | C | 1 | a0001c0001t0002g0347 | 1 | NA18945.hp1 | splice_region_variant&intron_variant | LOW | c.185+4A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259267 | ||||||
| chr9:70259338
|
G | A | 1 | a0001c0010t0002g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.185+75G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259338 | ||||||
| chr9:70259373
|
G | A | 5 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+110G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259373 | ||||||
| chr9:70259393
|
C | G | 1 | a0003c0003t0001g0346 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.185+130C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259393 | ||||||
| chr9:70259430
|
A | G | 26 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(23): Show | 26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.185+167A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259430 | ||||||
| chr9:70259434
|
T | A | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+171T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259434 | ||||||
| chr9:70259434
|
T | G | 3 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027 | 3 | NA18947.hp1 NA18969.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.185+171T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259434 | ||||||
| chr9:70259437
|
C | T | 7 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(4): Show | 7 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+174C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259437 | ||||||
| chr9:70259556
|
G | T | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+293G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259556 | ||||||
| chr9:70259688
|
C | T | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+425C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259688 | ||||||
| chr9:70259715
|
G | T | 1 | a0002c0002t0001g0318 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.185+452G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259715 | ||||||
| chr9:70259777
|
C | T | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.185+514C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259777 | ||||||
| chr9:70259832
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.185+569C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259832 | ||||||
| chr9:70259927
|
C | CT | 9 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(6): Show | 9 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.185+681dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70259927 | |||||
| chr9:70259927
|
CT | C | 117 | a0001c0001t0002g0105a0002c0002t0001g0002a0002c0002t0001g0004others(114): Show | 123 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.185+681delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70259927 | |||||
| chr9:70259953
|
T | A | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.185+690T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259953 | ||||||
| chr9:70260158
|
G | T | 1 | a0002c0002t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.185+895G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260158 | ||||||
| chr9:70260174
|
G | A | 2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.185+911G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260174 | ||||||
| chr9:70260244
|
A | G | 1 | a0001c0005t0003g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.185+981A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260244 | ||||||
| chr9:70260282
|
A | G | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185+1019A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260282 | ||||||
| chr9:70260294
|
T | A | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.185+1031T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260294 | ||||||
| chr9:70260469
|
A | G | 1 | a0007c0012t0001g0107 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.185+1206A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260469 | ||||||
| chr9:70260817
|
C | T | 1 | a0003c0003t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.185+1554C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260817 | ||||||
| chr9:70260895
|
A | C | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+1632A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260895 | ||||||
| chr9:70261288
|
A | T | 1 | a0001c0001t0002g0313 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.185+2025A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70261288 | ||||||
| chr9:70261559
|
T | G | 1 | a0001c0001t0002g0316 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.185+2296T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70261559 | ||||||
| chr9:70261728
|
T | C | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185+2465T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70261728 | ||||||
| chr9:70262254
|
T | C | 7 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(4): Show | 7 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-2050T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262254 | ||||||
| chr9:70262533
|
G | A | 1 | a0004c0004t0001g0320 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.186-1771G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262533 | ||||||
| chr9:70262621
|
A | G | 2 | a0003c0003t0001g0312a0004c0004t0001g0343 | 2 | HG02615.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.186-1683A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262621 | ||||||
| chr9:70262642
|
A | C | 64 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(61): Show | 66 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.186-1662A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262642 | ||||||
| chr9:70262935
|
G | A | 5 | a0001c0001t0002g0105a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG01978.hp1 NA19004.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-1369G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262935 | ||||||
| chr9:70262959
|
C | CA | 59 | a0001c0001t0002g0313a0001c0005t0003g0022a0002c0002t0001g0002others(56): Show | 63 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.186-1332dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70262959 | |||||
| chr9:70262967
|
A | G | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.186-1337A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262967 | ||||||
| chr9:70263022
|
G | A | 26 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(23): Show | 26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.186-1282G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263022 | ||||||
| chr9:70263114
|
T | C | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.186-1190T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263114 | ||||||
| chr9:70263143
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186-1161A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263143 | ||||||
| chr9:70263206
|
G | C | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.186-1098G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263206 | ||||||
| chr9:70263244
|
C | T | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.186-1060C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263244 | ||||||
| chr9:70263431
|
G | GA | 26 | a0001c0001t0002g0008a0001c0001t0002g0120a0001c0001t0002g0121others(23): Show | 27 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.186-871dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70263431 | |||||
| chr9:70263689
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186-615T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263689 | ||||||
| chr9:70263778
|
C | T | 1 | a0003c0003t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186-526C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263778 | ||||||
| chr9:70263813
|
A | G | 13 | a0002c0002t0001g0005a0002c0002t0001g0059a0002c0002t0001g0060others(10): Show | 14 | HG00597.hp2 HG02523.hp1 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-491A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263813 | ||||||
| chr9:70263908
|
A | C | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.186-396A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263908 | ||||||
| chr9:70263957
|
G | A | 1 | a0001c0005t0003g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-347G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263957 | ||||||
| chr9:70263962
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.186-342G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263962 | ||||||
| chr9:70264106
|
TTTAG | T | 5 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(2): Show | 5 | HG00544.hp2 HG00609.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-194_186-191del others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70264106 | |||||
| chr9:70264140
|
A | G | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.186-164A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70264140 | ||||||
| chr9:70264559
|
C | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.327+114C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264559 | ||||||
| chr9:70264623
|
T | C | 129 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(126): Show | 135 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.327+178T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264623 | ||||||
| chr9:70264684
|
G | A | 1 | a0003c0003t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327+239G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264684 | ||||||
| chr9:70264706
|
C | G | 1 | a0002c0002t0004g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.327+261C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264706 | ||||||
| chr9:70264748
|
AC | A | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+304delC | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264748 | ||||||
| chr9:70264859
|
G | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.327+414G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264859 | ||||||
| chr9:70264898
|
T | C | 6 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(3): Show | 6 | HG00738.hp2 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+453T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264898 | ||||||
| chr9:70265079
|
A | T | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+634A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265079 | ||||||
| chr9:70265156
|
A | G | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.327+711A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265156 | ||||||
| chr9:70265201
|
G | A | 32 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(29): Show | 34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.327+756G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265201 | ||||||
| chr9:70265204
|
C | T | 1 | a0003c0003t0001g0312 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.327+759C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265204 | ||||||
| chr9:70265328
|
G | A | 1 | a0002c0002t0001g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.327+883G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265328 | ||||||
| chr9:70265338
|
A | T | 1 | a0004c0004t0001g0343 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.327+893A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265338 | ||||||
| chr9:70265635
|
A | T | 1 | a0001c0001t0002g0303 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.327+1190A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265635 | ||||||
| chr9:70265758
|
A | G | 1 | a0001c0001t0002g0302 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.327+1313A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265758 | ||||||
| chr9:70266285
|
T | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.328-1638T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266285 | ||||||
| chr9:70266307
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.328-1616T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266307 | ||||||
| chr9:70266320
|
C | G | 1 | a0002c0002t0001g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.328-1603C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266320 | ||||||
| chr9:70266335
|
T | G | 1 | a0002c0002t0001g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.328-1588T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266335 | ||||||
| chr9:70266393
|
A | G | 1 | a0003c0003t0001g0202 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.328-1530A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266393 | ||||||
| chr9:70266831
|
C | A | 131 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(128): Show | 138 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.328-1092C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266831 | ||||||
| chr9:70266850
|
A | G | 1 | a0002c0002t0001g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.328-1073A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266850 | ||||||
| chr9:70267032
|
CT | C | 120 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(117): Show | 126 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.328-875delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr9 | 70267032 | |||||
| chr9:70267082
|
A | G | 1 | a0003c0003t0001g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.328-841A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267082 | ||||||
| chr9:70267095
|
A | G | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.328-828A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267095 | ||||||
| chr9:70267329
|
A | G | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.328-594A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267329 | ||||||
| chr9:70267472
|
T | C | 1 | a0002c0002t0001g0072 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.328-451T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267472 | ||||||
| chr9:70267539
|
T | C | 1 | a0003c0003t0001g0151 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.328-384T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267539 | ||||||
| chr9:70267581
|
G | A | 4 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(1): Show | 4 | NA18950.hp2 NA18995.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-342G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267581 | ||||||
| chr9:70267726
|
A | G | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.328-197A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267726 | ||||||
| chr9:70267859
|
A | G | 3 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308 | 3 | NA18965.hp1 NA18966.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.328-64A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267859 | ||||||
| chr9:70267876
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.328-47C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267876 | ||||||
| chr9:70267920
|
T | C | 3 | a0004c0004t0001g0321a0004c0004t0001g0322a0004c0004t0001g0323 | 3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
splice_region_variant&intron_variant | LOW | c.328-3T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267920 | ||||||
| chr9:70268119
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+144T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268119 | ||||||
| chr9:70268462
|
C | A | 63 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(60): Show | 65 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.380+487C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268462 | ||||||
| chr9:70268462
|
C | CA | 53 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(50): Show | 57 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.380+497dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70268462 | |||||
| chr9:70268524
|
C | T | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.380+549C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268524 | ||||||
| chr9:70268697
|
T | G | 1 | a0003c0003t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.380+722T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268697 | ||||||
| chr9:70268698
|
T | C | 1 | a0003c0003t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.380+723T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268698 | ||||||
| chr9:70268780
|
G | C | 6 | a0003c0003t0001g0145a0003c0003t0001g0152a0003c0003t0001g0153others(3): Show | 6 | HG01496.hp2 HG02300.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.380+805G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268780 | ||||||
| chr9:70269206
|
A | G | 1 | a0004c0004t0001g0341 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.380+1231A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70269206 | ||||||
| chr9:70269439
|
A | C | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380+1464A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70269439 | ||||||
| chr9:70270095
|
A | T | 1 | a0002c0002t0001g0057 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.380+2120A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270095 | ||||||
| chr9:70270115
|
C | T | 3 | a0004c0004t0001g0321a0004c0004t0001g0322a0004c0004t0001g0323 | 3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.380+2140C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270115 | ||||||
| chr9:70270117
|
A | C | 1 | a0010c0016t0002g0301 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.380+2142A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270117 | ||||||
| chr9:70270161
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+2186T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270161 | ||||||
| chr9:70270189
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+2214C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270189 | ||||||
| chr9:70270351
|
T | C | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.380+2376T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270351 | ||||||
| chr9:70270376
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+2401C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270376 | ||||||
| chr9:70270458
|
A | T | 1 | a0004c0004t0001g0320 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.380+2483A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270458 | ||||||
| chr9:70270459
|
T | C | 1 | a0002c0002t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.380+2484T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270459 | ||||||
| chr9:70270549
|
G | C | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.380+2574G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270549 | ||||||
| chr9:70270642
|
A | AT | 28 | a0001c0001t0002g0144a0001c0001t0002g0203a0001c0001t0002g0206others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.380+2691dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70270642 | |||||
| chr9:70270642
|
A | ATT | 88 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(85): Show | 94 | HG00099.hp2 HG00597.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.380+2690_380+2691d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70270642 | |||||
| chr9:70270642
|
A | ATTT | 16 | a0002c0002t0001g0027a0002c0002t0001g0056a0002c0002t0001g0057others(13): Show | 16 | HG01099.hp1 HG01106.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.380+2689_380+2691d others(5): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70270642 | |||||
| chr9:70270642
|
AT | A | 64 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0115others(61): Show | 68 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.380+2691delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70270642 | |||||
| chr9:70270710
|
A | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+2735A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270710 | ||||||
| chr9:70270725
|
C | G | 1 | a0004c0008t0005g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.380+2750C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270725 | ||||||
| chr9:70270844
|
G | A | 12 | a0003c0003t0001g0156a0003c0003t0001g0157a0003c0003t0001g0158others(9): Show | 12 | HG01361.hp1 HG01978.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.380+2869G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270844 | ||||||
| chr9:70270893
|
C | T | 111 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.380+2918C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270893 | ||||||
| chr9:70270902
|
C | G | 1 | a0001c0001t0002g0296 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.380+2927C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270902 | ||||||
| chr9:70271005
|
G | A | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.380+3030G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271005 | ||||||
| chr9:70271105
|
A | T | 1 | a0001c0001t0002g0253 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.380+3130A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271105 | ||||||
| chr9:70271141
|
GTTTTGGA others(10): Show |
G | 225 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(222): Show | 238 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.380+3182_380+3198d others(19): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70271141 | |||||
| chr9:70271212
|
A | T | 1 | a0003c0003t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.380+3237A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271212 | ||||||
| chr9:70271340
|
G | A | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+3365G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271340 | ||||||
| chr9:70271437
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+3462A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271437 | ||||||
| chr9:70271610
|
A | G | 1 | a0014c0018t0001g0196 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.380+3635A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271610 | ||||||
| chr9:70271624
|
G | A | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380+3649G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271624 | ||||||
| chr9:70271733
|
G | A | 2 | a0001c0001t0002g0212a0001c0001t0002g0259 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.380+3758G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271733 | ||||||
| chr9:70271786
|
G | A | 1 | a0002c0002t0001g0030 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.380+3811G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271786 | ||||||
| chr9:70272113
|
C | G | 1 | a0001c0001t0023g0252 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.380+4138C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272113 | ||||||
| chr9:70272127
|
A | C | 1 | a0001c0001t0023g0252 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.380+4152A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272127 | ||||||
| chr9:70272217
|
C | G | 1 | a0003c0003t0001g0195 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.380+4242C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272217 | ||||||
| chr9:70272494
|
T | A | 111 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.380+4519T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272494 | ||||||
| chr9:70272540
|
C | T | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.380+4565C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272540 | ||||||
| chr9:70272750
|
T | C | 1 | a0001c0001t0002g0303 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.381-4560T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272750 | ||||||
| chr9:70272769
|
A | C | 1 | a0004c0006t0001g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.381-4541A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272769 | ||||||
| chr9:70273049
|
G | C | 1 | a0002c0002t0022g0074 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.381-4261G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273049 | ||||||
| chr9:70273064
|
A | G | 1 | a0002c0002t0010g0055 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.381-4246A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273064 | ||||||
| chr9:70273189
|
C | CT | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.381-4110dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70273189 | |||||
| chr9:70273212
|
G | A | 1 | a0003c0003t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.381-4098G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273212 | ||||||
| chr9:70273326
|
A | AT | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.381-3979dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70273326 | |||||
| chr9:70273361
|
C | T | 32 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(29): Show | 32 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.381-3949C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273361 | ||||||
| chr9:70273470
|
A | G | 1 | a0002c0002t0001g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.381-3840A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273470 | ||||||
| chr9:70273596
|
C | T | 38 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.381-3714C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273596 | ||||||
| chr9:70273740
|
A | G | 2 | a0001c0001t0002g0105a0001c0001t0002g0118 | 2 | HG01978.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.381-3570A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273740 | ||||||
| chr9:70273974
|
A | G | 33 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(30): Show | 34 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.381-3336A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273974 | ||||||
| chr9:70274142
|
C | T | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.381-3168C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274142 | ||||||
| chr9:70274171
|
T | C | 1 | a0003c0003t0001g0146 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381-3139T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274171 | ||||||
| chr9:70274183
|
G | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.381-3127G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274183 | ||||||
| chr9:70274207
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-3103G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274207 | ||||||
| chr9:70274275
|
G | T | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142others(2): Show | 5 | HG00544.hp1 HG00642.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-3035G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274275 | ||||||
| chr9:70274324
|
A | G | 1 | a0004c0004t0001g0343 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.381-2986A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274324 | ||||||
| chr9:70274377
|
G | A | 5 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-2933G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274377 | ||||||
| chr9:70274469
|
C | CT | 6 | a0001c0001t0002g0295a0004c0008t0005g0100a0004c0008t0005g0101others(3): Show | 6 | HG00738.hp2 HG01433.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.381-2829dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70274469 | |||||
| chr9:70274470
|
T | C | 1 | a0002c0002t0001g0112 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.381-2840T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274470 | ||||||
| chr9:70274496
|
A | C | 48 | a0003c0003t0001g0010a0003c0003t0001g0119a0003c0003t0001g0145others(45): Show | 49 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.381-2814A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274496 | ||||||
| chr9:70274548
|
T | C | 7 | a0003c0003t0001g0174a0003c0003t0001g0176a0003c0003t0001g0177others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.381-2762T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274548 | ||||||
| chr9:70274565
|
A | T | 1 | a0001c0005t0003g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.381-2745A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274565 | ||||||
| chr9:70274880
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-2430G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274880 | ||||||
| chr9:70274908
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381-2402A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274908 | ||||||
| chr9:70274933
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-2377A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274933 | ||||||
| chr9:70274996
|
C | A | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381-2314C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274996 | ||||||
| chr9:70275347
|
C | T | 60 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0106others(57): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.381-1963C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275347 | ||||||
| chr9:70275415
|
G | A | 2 | a0003c0003t0001g0147a0003c0003t0001g0312 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.381-1895G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275415 | ||||||
| chr9:70275446
|
C | G | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381-1864C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275446 | ||||||
| chr9:70275493
|
A | G | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381-1817A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275493 | ||||||
| chr9:70275505
|
T | G | 6 | a0002c0002t0001g0004a0002c0002t0001g0031a0002c0002t0001g0032others(3): Show | 7 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.381-1805T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275505 | ||||||
| chr9:70275516
|
AATGTGAA others(53): Show |
A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-1685_381-1626d others(62): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70275516 | |||||
| chr9:70275615
|
C | A | 32 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(29): Show | 32 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.381-1695C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275615 | ||||||
| chr9:70275710
|
T | C | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-1600T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275710 | ||||||
| chr9:70275798
|
G | A | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.381-1512G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275798 | ||||||
| chr9:70275938
|
G | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-1372G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275938 | ||||||
| chr9:70275998
|
TG | T | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-1311delG | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275998 | ||||||
| chr9:70276070
|
G | A | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-1240G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276070 | ||||||
| chr9:70276232
|
C | A | 1 | a0001c0001t0002g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.381-1078C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276232 | ||||||
| chr9:70276659
|
T | C | 1 | a0003c0003t0001g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.381-651T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276659 | ||||||
| chr9:70276722
|
C | T | 1 | a0002c0002t0004g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.381-588C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276722 | ||||||
| chr9:70276911
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.381-399G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276911 | ||||||
| chr9:70276912
|
G | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.381-398G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276912 | ||||||
| chr9:70277022
|
C | T | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.381-288C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70277022 | ||||||
| chr9:70277534
|
G | A | 2 | a0003c0003t0001g0145a0003c0003t0001g0152 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.543+62G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277534 | ||||||
| chr9:70277718
|
A | G | 1 | a0002c0002t0001g0071 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.543+246A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277718 | ||||||
| chr9:70277756
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.543+284C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277756 | ||||||
| chr9:70277759
|
T | C | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+287T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277759 | ||||||
| chr9:70277803
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+331A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277803 | ||||||
| chr9:70277854
|
CTATATT | C | 9 | a0004c0004t0001g0324a0004c0004t0001g0325a0004c0004t0001g0326others(6): Show | 9 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+387_543+392del others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr9 | 70277854 | |||||
| chr9:70277993
|
T | C | 1 | a0003c0003t0008g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-498T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277993 | ||||||
| chr9:70278020
|
CAAT | C | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.544-470_544-468del others(3): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70278020 | ||||||
| chr9:70278077
|
T | C | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-414T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70278077 | ||||||
| chr9:70278126
|
G | A | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-365G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70278126 | ||||||
| chr9:70278382
|
GT | G | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.544-101delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr9 | 70278382 | |||||
| chr9:70278433
|
A | T | 1 | a0001c0001t0002g0294 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.544-58A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70278433 | ||||||
| chr9:70278663
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.678+38T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278663 | ||||||
| chr9:70278701
|
A | G | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+76A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278701 | ||||||
| chr9:70278775
|
G | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.678+150G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278775 | ||||||
| chr9:70278838
|
C | T | 2 | a0003c0003t0001g0193a0003c0003t0020g0194 | 2 | HG02165.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.678+213C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278838 | ||||||
| chr9:70278928
|
A | G | 1 | a0001c0005t0003g0022 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.678+303A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278928 | ||||||
| chr9:70279181
|
C | T | 1 | a0002c0002t0001g0056 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.678+556C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279181 | ||||||
| chr9:70279266
|
A | C | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.678+641A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279266 | ||||||
| chr9:70279407
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.678+782C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279407 | ||||||
| chr9:70279415
|
A | T | 1 | a0001c0005t0003g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.678+790A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279415 | ||||||
| chr9:70279513
|
T | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.678+888T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279513 | ||||||
| chr9:70279661
|
A | G | 6 | a0002c0002t0004g0007a0002c0002t0004g0084a0002c0002t0004g0085others(3): Show | 7 | HG01943.hp1 HG01975.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.678+1036A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279661 | ||||||
| chr9:70279674
|
G | A | 1 | a0001c0001t0002g0262 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.678+1049G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279674 | ||||||
| chr9:70279678
|
G | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.678+1053G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279678 | ||||||
| chr9:70279689
|
C | T | 1 | a0002c0002t0001g0054 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.678+1064C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279689 | ||||||
| chr9:70279732
|
G | A | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.679-1027G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279732 | ||||||
| chr9:70279813
|
G | A | 2 | a0001c0010t0002g0016a0001c0010t0002g0263 | 2 | HG02040.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.679-946G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279813 | ||||||
| chr9:70279817
|
C | CA | 14 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0264others(11): Show | 14 | HG00544.hp1 HG00733.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.679-921dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr9 | 70279817 | |||||
| chr9:70279817
|
CA | C | 33 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0261others(30): Show | 35 | HG00323.hp1 HG00609.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.679-921delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr9 | 70279817 | |||||
| chr9:70279817
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0001g0053 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.679-931_679-921del others(11): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr9 | 70279817 | |||||
| chr9:70279911
|
G | A | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.679-848G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279911 | ||||||
| chr9:70280080
|
G | A | 1 | a0001c0005t0003g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.679-679G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280080 | ||||||
| chr9:70280131
|
G | A | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.679-628G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280131 | ||||||
| chr9:70280208
|
C | T | 1 | a0003c0003t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.679-551C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280208 | ||||||
| chr9:70280426
|
A | G | 1 | a0003c0003t0001g0172 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.679-333A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280426 | ||||||
| chr9:70280449
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.679-310A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280449 | ||||||
| chr9:70280466
|
T | G | 5 | a0004c0006t0001g0331a0004c0006t0001g0332a0004c0006t0001g0333others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.679-293T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280466 | ||||||
| chr9:70280928
|
C | T | 1 | a0001c0001t0002g0248 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.819+29C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70280928 | ||||||
| chr9:70281107
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.819+208G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281107 | ||||||
| chr9:70281112
|
A | T | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.819+213A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281112 | ||||||
| chr9:70281133
|
G | A | 1 | a0004c0004t0001g0334 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.819+234G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281133 | ||||||
| chr9:70281193
|
C | T | 1 | a0003c0003t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.819+294C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281193 | ||||||
| chr9:70281204
|
C | T | 2 | a0003c0003t0001g0155a0003c0003t0001g0201 | 2 | HG01496.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.819+305C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281204 | ||||||
| chr9:70281262
|
G | A | 4 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0002g0143others(1): Show | 4 | HG00544.hp1 HG00642.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+363G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281262 | ||||||
| chr9:70281267
|
C | A | 120 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(117): Show | 126 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.819+368C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281267 | ||||||
| chr9:70281319
|
T | C | 122 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(119): Show | 128 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.819+420T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281319 | ||||||
| chr9:70281332
|
G | A | 3 | a0001c0001t0002g0203a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG01175.hp1 HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.819+433G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281332 | ||||||
| chr9:70281512
|
G | A | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.819+613G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281512 | ||||||
| chr9:70281543
|
G | A | 2 | a0004c0004t0001g0337a0004c0004t0001g0338 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.819+644G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281543 | ||||||
| chr9:70281571
|
T | C | 3 | a0003c0003t0001g0156a0003c0003t0001g0157a0003c0003t0001g0166 | 3 | NA18987.hp2 NA19055.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.819+672T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281571 | ||||||
| chr9:70281683
|
G | C | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820-739G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281683 | ||||||
| chr9:70281749
|
G | A | 1 | a0002c0002t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.820-673G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281749 | ||||||
| chr9:70281780
|
A | G | 1 | a0004c0004t0001g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.820-642A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281780 | ||||||
| chr9:70281842
|
CT | C | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.820-573delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr9 | 70281842 | |||||
| chr9:70281850
|
C | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.820-572C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281850 | ||||||
| chr9:70281898
|
T | A | 1 | a0001c0010t0002g0263 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.820-524T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281898 | ||||||
| chr9:70281959
|
G | A | 1 | a0003c0003t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.820-463G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281959 | ||||||
| chr9:70282039
|
G | GT | 6 | a0001c0001t0002g0292a0001c0001t0007g0290a0001c0001t0007g0291others(3): Show | 6 | HG00738.hp1 HG01070.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-371dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr9 | 70282039 | |||||
| chr9:70282041
|
T | G | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-381T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282041 | ||||||
| chr9:70282051
|
T | TTC | 117 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(114): Show | 123 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.820-371_820-370ins others(2): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282051 | ||||||
| chr9:70282172
|
G | T | 1 | a0001c0001t0002g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.820-250G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282172 | ||||||
| chr9:70282213
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.820-209G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282213 | ||||||
| chr9:70282384
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.820-38G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282384 | ||||||
| chr9:70282600
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.981+17A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70282600 | ||||||
| chr9:70282625
|
T | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.981+42T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70282625 | ||||||
| chr9:70282857
|
C | T | 6 | a0003c0003t0001g0003a0003c0003t0001g0168a0003c0003t0001g0169others(3): Show | 8 | HG02109.hp1 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+274C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70282857 | ||||||
| chr9:70282997
|
A | G | 1 | a0003c0003t0008g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.981+414A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70282997 | ||||||
| chr9:70283054
|
A | G | 57 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(54): Show | 59 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.981+471A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283054 | ||||||
| chr9:70283109
|
G | A | 7 | a0004c0004t0001g0344a0004c0008t0005g0100a0004c0008t0005g0101others(4): Show | 7 | HG00738.hp2 HG01433.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+526G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283109 | ||||||
| chr9:70283192
|
A | C | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.981+609A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283192 | ||||||
| chr9:70283235
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.981+652G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283235 | ||||||
| chr9:70283238
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.981+655C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283238 | ||||||
| chr9:70283625
|
C | T | 1 | a0002c0002t0001g0083 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.981+1042C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283625 | ||||||
| chr9:70283717
|
T | C | 1 | a0015c0020t0006g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.981+1134T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283717 | ||||||
| chr9:70283795
|
A | AT | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.981+1221dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr9 | 70283795 | |||||
| chr9:70283977
|
T | G | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.981+1394T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283977 | ||||||
| chr9:70284173
|
C | T | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.981+1590C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284173 | ||||||
| chr9:70284225
|
A | C | 1 | a0004c0004t0001g0339 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.981+1642A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284225 | ||||||
| chr9:70284358
|
A | G | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.981+1775A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284358 | ||||||
| chr9:70284556
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.982-1644A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284556 | ||||||
| chr9:70284567
|
G | C | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.982-1633G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284567 | ||||||
| chr9:70284610
|
C | G | 2 | a0003c0003t0001g0193a0003c0003t0020g0194 | 2 | HG02165.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.982-1590C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284610 | ||||||
| chr9:70284641
|
A | T | 1 | a0001c0005t0003g0022 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.982-1559A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284641 | ||||||
| chr9:70284649
|
C | T | 1 | a0002c0002t0001g0052 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.982-1551C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284649 | ||||||
| chr9:70284740
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.982-1460G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284740 | ||||||
| chr9:70284890
|
AT | A | 28 | a0001c0001t0002g0305a0002c0002t0001g0006a0002c0002t0001g0071others(25): Show | 30 | HG00609.hp2 HG00673.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.982-1298delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr9 | 70284890 | |||||
| chr9:70284904
|
A | G | 1 | a0003c0003t0001g0346 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.982-1296A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284904 | ||||||
| chr9:70284920
|
G | A | 341 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(338): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.982-1280G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284920 | ||||||
| chr9:70284951
|
A | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.982-1249A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284951 | ||||||
| chr9:70285024
|
T | TA | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-1175dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr9 | 70285024 | |||||
| chr9:70285238
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.982-962A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285238 | ||||||
| chr9:70285294
|
A | C | 6 | a0001c0001t0002g0120a0001c0001t0002g0243a0001c0001t0002g0244others(3): Show | 6 | HG00438.hp1 HG00597.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-906A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285294 | ||||||
| chr9:70285373
|
A | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.982-827A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285373 | ||||||
| chr9:70285432
|
G | A | 8 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0255others(5): Show | 8 | HG02486.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-768G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285432 | ||||||
| chr9:70285443
|
A | G | 25 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0122others(22): Show | 26 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.982-757A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285443 | ||||||
| chr9:70285583
|
A | G | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-617A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285583 | ||||||
| chr9:70285638
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.982-562G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285638 | ||||||
| chr9:70285802
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.982-398A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285802 | ||||||
| chr9:70285868
|
A | G | 2 | a0004c0004t0001g0329a0004c0004t0001g0330 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.982-332A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285868 | ||||||
| chr9:70286176
|
C | T | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.982-24C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70286176 | ||||||
| chr9:70286180
|
T | C | 339 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(336): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.982-20T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70286180 | ||||||
| chr9:70286343
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+72A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286343 | ||||||
| chr9:70286404
|
G | T | 5 | a0001c0001t0002g0212a0001c0001t0002g0242a0001c0001t0002g0259others(2): Show | 5 | HG02647.hp2 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+133G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286404 | ||||||
| chr9:70286490
|
T | C | 1 | a0004c0004t0001g0337 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1053+219T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286490 | ||||||
| chr9:70286562
|
G | C | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1053+291G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286562 | ||||||
| chr9:70286639
|
T | C | 4 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+368T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286639 | ||||||
| chr9:70286650
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1053+379C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286650 | ||||||
| chr9:70286651
|
G | T | 5 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+380G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286651 | ||||||
| chr9:70286717
|
C | CT | 10 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0139others(7): Show | 10 | HG02145.hp2 HG02300.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1053+467dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70286717 | |||||
| chr9:70286717
|
CT | C | 121 | a0001c0001t0002g0123a0001c0005t0003g0018a0001c0005t0003g0019others(118): Show | 126 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.1053+467delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70286717 | |||||
| chr9:70286717
|
CTT | C | 6 | a0002c0002t0001g0088a0002c0002t0001g0090a0003c0003t0001g0145others(3): Show | 6 | HG00323.hp1 HG01099.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+466_1053+467d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70286717 | |||||
| chr9:70286991
|
G | A | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1053+720G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286991 | ||||||
| chr9:70287109
|
C | A | 2 | a0001c0001t0002g0215a0001c0001t0015g0266 | 2 | NA18944.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1053+838C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287109 | ||||||
| chr9:70287149
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053+878A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287149 | ||||||
| chr9:70287156
|
A | T | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053+885A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287156 | ||||||
| chr9:70287159
|
T | G | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053+888T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287159 | ||||||
| chr9:70287470
|
A | G | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1053+1199A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287470 | ||||||
| chr9:70287485
|
T | G | 1 | a0001c0001t0002g0267 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1053+1214T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287485 | ||||||
| chr9:70287501
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+1230A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287501 | ||||||
| chr9:70287583
|
T | C | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+1312T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287583 | ||||||
| chr9:70287587
|
G | A | 55 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0119others(52): Show | 58 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1053+1316G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287587 | ||||||
| chr9:70287591
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+1320A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287591 | ||||||
| chr9:70287755
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+1484G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287755 | ||||||
| chr9:70287820
|
AAGAATTT others(18): Show |
A | 1 | a0002c0002t0001g0082 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1550_1053+157 others(29): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287820 | ||||||
| chr9:70287829
|
TG | T | 25 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(22): Show | 27 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1053+1562delG | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70287829 | |||||
| chr9:70287846
|
T | G | 1 | a0002c0002t0001g0082 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1575T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287846 | ||||||
| chr9:70287848
|
T | C | 1 | a0002c0002t0001g0082 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1577T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287848 | ||||||
| chr9:70287849
|
A | C | 1 | a0002c0002t0001g0082 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1578A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287849 | ||||||
| chr9:70287851
|
T | A | 1 | a0002c0002t0001g0082 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1580T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287851 | ||||||
| chr9:70288041
|
C | T | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1053+1770C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288041 | ||||||
| chr9:70288088
|
T | C | 1 | a0015c0020t0006g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1053+1817T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288088 | ||||||
| chr9:70288116
|
G | C | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1053+1845G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288116 | ||||||
| chr9:70288238
|
G | A | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+1967G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288238 | ||||||
| chr9:70288238
|
G | T | 64 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(61): Show | 66 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1053+1967G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288238 | ||||||
| chr9:70288445
|
A | T | 5 | a0004c0004t0001g0321a0004c0004t0001g0322a0004c0004t0001g0323others(2): Show | 5 | HG01099.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+2174A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288445 | ||||||
| chr9:70288455
|
TTTA | T | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1053+2187_1053+218 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70288455 | |||||
| chr9:70288499
|
A | G | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1053+2228A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288499 | ||||||
| chr9:70288528
|
T | C | 1 | a0007c0012t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1053+2257T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288528 | ||||||
| chr9:70288851
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1053+2580G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288851 | ||||||
| chr9:70288983
|
T | C | 4 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+2712T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288983 | ||||||
| chr9:70288991
|
C | T | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+2720C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288991 | ||||||
| chr9:70289026
|
A | G | 1 | a0002c0002t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1053+2755A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289026 | ||||||
| chr9:70289060
|
C | T | 2 | a0004c0004t0001g0329a0004c0004t0001g0330 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1053+2789C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289060 | ||||||
| chr9:70289064
|
G | T | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+2793G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289064 | ||||||
| chr9:70289074
|
G | A | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1053+2803G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289074 | ||||||
| chr9:70289132
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0143 | 2 | HG00544.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1053+2861G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289132 | ||||||
| chr9:70289239
|
C | T | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1053+2968C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289239 | ||||||
| chr9:70289303
|
G | A | 339 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(336): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1053+3032G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289303 | ||||||
| chr9:70289532
|
G | A | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1053+3261G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289532 | ||||||
| chr9:70289875
|
A | ATAT | 40 | a0001c0001t0021g0317a0001c0005t0003g0022a0002c0002t0001g0059others(37): Show | 40 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.1053+3627_1053+362 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70289875 | |||||
| chr9:70289875
|
A | ATATTAT | 29 | a0002c0002t0001g0006a0002c0002t0001g0030a0002c0002t0001g0038others(26): Show | 31 | HG00673.hp1 HG00673.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1053+3624_1053+362 others(10): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70289875 | |||||
| chr9:70289961
|
C | G | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+3690C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289961 | ||||||
| chr9:70289969
|
G | A | 2 | a0004c0004t0001g0335a0004c0004t0001g0339 | 2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1053+3698G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289969 | ||||||
| chr9:70290052
|
A | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0105others(58): Show | 65 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1053+3781A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290052 | ||||||
| chr9:70290446
|
G | A | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1053+4175G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290446 | ||||||
| chr9:70290488
|
G | A | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1053+4217G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290488 | ||||||
| chr9:70290558
|
T | C | 1 | a0001c0001t0017g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1053+4287T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290558 | ||||||
| chr9:70290825
|
A | T | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+4554A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290825 | ||||||
| chr9:70290839
|
A | G | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+4568A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290839 | ||||||
| chr9:70291006
|
T | G | 7 | a0001c0001t0002g0213a0001c0001t0002g0219a0001c0001t0002g0220others(4): Show | 7 | HG00735.hp1 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1053+4735T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291006 | ||||||
| chr9:70291128
|
CTAGT | C | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1053+4859_1053+486 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70291128 | |||||
| chr9:70291168
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+4897T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291168 | ||||||
| chr9:70291196
|
G | A | 5 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+4925G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291196 | ||||||
| chr9:70291235
|
T | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+4964T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291235 | ||||||
| chr9:70291553
|
A | G | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+5282A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291553 | ||||||
| chr9:70291610
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1053+5339A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291610 | ||||||
| chr9:70291755
|
A | G | 4 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0051others(1): Show | 4 | NA18953.hp1 NA18963.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+5484A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291755 | ||||||
| chr9:70291778
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053+5507C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291778 | ||||||
| chr9:70291845
|
AT | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1053+5586delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70291845 | |||||
| chr9:70291925
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+5654A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291925 | ||||||
| chr9:70291972
|
T | G | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1053+5701T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291972 | ||||||
| chr9:70291985
|
G | A | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+5714G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291985 | ||||||
| chr9:70292052
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+5781A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292052 | ||||||
| chr9:70292176
|
AC | A | 60 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0106others(57): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1054-5788delC | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70292176 | |||||
| chr9:70292228
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1054-5738G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292228 | ||||||
| chr9:70292293
|
C | T | 1 | a0003c0003t0001g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1054-5673C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292293 | ||||||
| chr9:70292341
|
T | C | 1 | a0003c0003t0001g0159 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1054-5625T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292341 | ||||||
| chr9:70292345
|
A | G | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-5621A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292345 | ||||||
| chr9:70292349
|
G | A | 1 | a0003c0003t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1054-5617G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292349 | ||||||
| chr9:70292451
|
A | C | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1054-5515A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292451 | ||||||
| chr9:70292691
|
A | G | 1 | a0001c0001t0002g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1054-5275A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292691 | ||||||
| chr9:70292791
|
T | C | 5 | a0004c0004t0001g0325a0004c0004t0001g0326a0004c0004t0001g0329others(2): Show | 5 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-5175T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292791 | ||||||
| chr9:70292897
|
C | T | 1 | a0003c0003t0001g0165 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1054-5069C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292897 | ||||||
| chr9:70293156
|
G | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-4810G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293156 | ||||||
| chr9:70293265
|
A | G | 1 | a0003c0003t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1054-4701A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293265 | ||||||
| chr9:70293380
|
C | G | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1054-4586C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293380 | ||||||
| chr9:70293458
|
C | G | 64 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(61): Show | 66 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1054-4508C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293458 | ||||||
| chr9:70293535
|
T | G | 1 | a0004c0006t0001g0342 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1054-4431T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293535 | ||||||
| chr9:70293580
|
A | G | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1054-4386A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293580 | ||||||
| chr9:70293588
|
C | T | 38 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1054-4378C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293588 | ||||||
| chr9:70293839
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-4127T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293839 | ||||||
| chr9:70293963
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1054-4003G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293963 | ||||||
| chr9:70294079
|
G | C | 2 | a0001c0001t0002g0215a0001c0001t0015g0266 | 2 | NA18944.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1054-3887G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294079 | ||||||
| chr9:70294196
|
G | A | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-3770G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294196 | ||||||
| chr9:70294331
|
G | A | 2 | a0002c0002t0001g0091a0002c0002t0001g0092 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054-3635G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294331 | ||||||
| chr9:70294422
|
A | G | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1054-3544A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294422 | ||||||
| chr9:70294489
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-3477G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294489 | ||||||
| chr9:70294706
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1054-3260A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294706 | ||||||
| chr9:70294817
|
G | C | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1054-3149G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294817 | ||||||
| chr9:70295046
|
A | T | 38 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1054-2920A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295046 | ||||||
| chr9:70295066
|
C | T | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1054-2900C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295066 | ||||||
| chr9:70295069
|
C | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-2897C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295069 | ||||||
| chr9:70295203
|
C | A | 3 | a0003c0003t0001g0174a0003c0003t0001g0177a0003c0003t0001g0199 | 3 | HG00099.hp1 HG00323.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1054-2763C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295203 | ||||||
| chr9:70295232
|
A | G | 1 | a0001c0001t0002g0305 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1054-2734A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295232 | ||||||
| chr9:70295250
|
G | T | 2 | a0004c0004t0001g0324a0004c0004t0001g0343 | 2 | NA18955.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1054-2716G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295250 | ||||||
| chr9:70295301
|
TA | T | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1054-2654delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70295301 | |||||
| chr9:70295329
|
G | A | 1 | a0001c0001t0002g0268 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1054-2637G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295329 | ||||||
| chr9:70295361
|
C | T | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-2605C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295361 | ||||||
| chr9:70295363
|
C | T | 118 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(115): Show | 124 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1054-2603C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295363 | ||||||
| chr9:70295425
|
T | G | 1 | a0004c0004t0001g0339 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1054-2541T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295425 | ||||||
| chr9:70295470
|
C | CA | 60 | a0001c0001t0016g0297a0002c0002t0001g0006a0002c0002t0001g0037others(57): Show | 62 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1054-2479dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70295470 | |||||
| chr9:70295470
|
C | CAA | 50 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(47): Show | 54 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1054-2480_1054-247 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70295470 | |||||
| chr9:70295485
|
A | G | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1054-2481A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295485 | ||||||
| chr9:70295515
|
A | G | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-2451A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295515 | ||||||
| chr9:70295577
|
C | T | 1 | a0003c0003t0001g0202 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1054-2389C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295577 | ||||||
| chr9:70295649
|
G | A | 1 | a0002c0002t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1054-2317G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295649 | ||||||
| chr9:70295681
|
A | G | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-2285A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295681 | ||||||
| chr9:70295705
|
G | A | 3 | a0004c0004t0001g0321a0004c0004t0001g0322a0004c0004t0001g0323 | 3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1054-2261G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295705 | ||||||
| chr9:70295748
|
C | T | 3 | a0001c0001t0002g0203a0001c0001t0002g0217a0001c0001t0002g0283 | 3 | HG01168.hp2 HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1054-2218C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295748 | ||||||
| chr9:70295764
|
C | A | 4 | a0003c0003t0001g0010a0003c0003t0001g0182a0003c0003t0001g0183others(1): Show | 5 | NA18940.hp2 NA18954.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-2202C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295764 | ||||||
| chr9:70295817
|
G | A | 60 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0106others(57): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1054-2149G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295817 | ||||||
| chr9:70295833
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-2133G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295833 | ||||||
| chr9:70295885
|
A | G | 1 | a0003c0003t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1054-2081A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295885 | ||||||
| chr9:70295909
|
G | A | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1054-2057G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295909 | ||||||
| chr9:70295968
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1054-1998C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295968 | ||||||
| chr9:70295971
|
T | C | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-1995T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295971 | ||||||
| chr9:70296036
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-1930G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296036 | ||||||
| chr9:70296269
|
A | G | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1054-1697A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296269 | ||||||
| chr9:70296318
|
A | G | 111 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1054-1648A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296318 | ||||||
| chr9:70296425
|
G | A | 8 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0255others(5): Show | 8 | HG02486.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-1541G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296425 | ||||||
| chr9:70296466
|
A | G | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1054-1500A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296466 | ||||||
| chr9:70296524
|
G | T | 38 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1054-1442G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296524 | ||||||
| chr9:70296532
|
A | G | 1 | a0001c0001t0002g0292 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1054-1434A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296532 | ||||||
| chr9:70296534
|
C | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-1432C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296534 | ||||||
| chr9:70296539
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-1427T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296539 | ||||||
| chr9:70296552
|
C | CA | 31 | a0002c0002t0001g0037a0002c0002t0001g0061a0002c0002t0013g0319others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054-1400dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70296552 | |||||
| chr9:70296552
|
C | CAA | 6 | a0004c0004t0001g0341a0004c0008t0005g0100a0004c0008t0005g0101others(3): Show | 6 | HG00140.hp2 HG00738.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054-1401_1054-140 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70296552 | |||||
| chr9:70296571
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-1395A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296571 | ||||||
| chr9:70296725
|
A | G | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-1241A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296725 | ||||||
| chr9:70296775
|
A | G | 1 | a0003c0003t0001g0346 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1054-1191A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296775 | ||||||
| chr9:70296962
|
C | G | 111 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1054-1004C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296962 | ||||||
| chr9:70296999
|
T | C | 1 | a0002c0002t0004g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1054-967T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296999 | ||||||
| chr9:70297014
|
TTATTTC | T | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-950_1054-945d others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70297014 | |||||
| chr9:70297047
|
C | CT | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-918dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70297047 | |||||
| chr9:70297059
|
C | G | 57 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(54): Show | 59 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1054-907C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297059 | ||||||
| chr9:70297133
|
T | C | 1 | a0001c0001t0002g0295 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1054-833T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297133 | ||||||
| chr9:70297202
|
G | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1054-764G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297202 | ||||||
| chr9:70297534
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-432A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297534 | ||||||
| chr9:70297540
|
A | G | 5 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-426A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297540 | ||||||
| chr9:70298800
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1309+579G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70298800 | ||||||
| chr9:70298844
|
C | G | 1 | a0003c0003t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1309+623C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70298844 | ||||||
| chr9:70298903
|
T | C | 1 | a0002c0002t0004g0084 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1309+682T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70298903 | ||||||
| chr9:70298993
|
T | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0125a0001c0001t0002g0126 | 4 | HG01074.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309+772T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70298993 | ||||||
| chr9:70299128
|
A | G | 26 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(23): Show | 26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1309+907A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299128 | ||||||
| chr9:70299307
|
A | G | 1 | a0004c0004t0001g0341 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1310-739A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299307 | ||||||
| chr9:70299336
|
T | A | 64 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(61): Show | 66 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1310-710T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299336 | ||||||
| chr9:70299436
|
C | T | 1 | a0003c0003t0001g0172 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1310-610C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299436 | ||||||
| chr9:70299586
|
A | C | 341 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(338): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1310-460A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299586 | ||||||
| chr9:70299627
|
T | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1310-419T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299627 | ||||||
| chr9:70299631
|
C | T | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1310-415C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299631 | ||||||
| chr9:70299657
|
TC | T | 56 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(53): Show | 60 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1310-380delC | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 70299657 | |||||
| chr9:70299732
|
A | G | 339 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(336): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1310-314A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299732 | ||||||
| chr9:70299733
|
G | T | 1 | a0003c0003t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1310-313G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299733 | ||||||
| chr9:70299787
|
T | TTTTG | 9 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(6): Show | 9 | HG01496.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1310-235_1310-232d others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 70299787 | |||||
| chr9:70299787
|
TTTTG | T | 58 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0119others(55): Show | 61 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1310-235_1310-232d others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 70299787 | |||||
| chr9:70300363
|
G | C | 1 | a0001c0001t0017g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1464+163G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300363 | ||||||
| chr9:70300374
|
G | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1464+174G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300374 | ||||||
| chr9:70300376
|
A | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1464+176A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300376 | ||||||
| chr9:70300434
|
T | C | 4 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0081others(1): Show | 4 | HG00673.hp2 NA18967.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464+234T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300434 | ||||||
| chr9:70300568
|
A | G | 6 | a0003c0003t0001g0145a0003c0003t0001g0152a0003c0003t0001g0153others(3): Show | 6 | HG01496.hp2 HG02300.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1464+368A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300568 | ||||||
| chr9:70300719
|
T | G | 1 | a0002c0002t0001g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1464+519T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300719 | ||||||
| chr9:70301027
|
C | T | 111 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1464+827C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301027 | ||||||
| chr9:70301623
|
C | T | 1 | a0004c0004t0001g0320 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1464+1423C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301623 | ||||||
| chr9:70301689
|
A | G | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1464+1489A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301689 | ||||||
| chr9:70301790
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1464+1590T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301790 | ||||||
| chr9:70301810
|
A | G | 38 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1464+1610A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301810 | ||||||
| chr9:70301878
|
A | G | 2 | a0001c0001t0002g0257a0001c0001t0002g0316 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1464+1678A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301878 | ||||||
| chr9:70302028
|
A | T | 1 | a0001c0001t0002g0316 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1464+1828A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302028 | ||||||
| chr9:70302040
|
C | A | 1 | a0001c0001t0002g0269 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1464+1840C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302040 | ||||||
| chr9:70302188
|
A | G | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1464+1988A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302188 | ||||||
| chr9:70302220
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1464+2020G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302220 | ||||||
| chr9:70302233
|
G | C | 106 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(103): Show | 114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1464+2033G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302233 | ||||||
| chr9:70302278
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1464+2078G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302278 | ||||||
| chr9:70302458
|
A | G | 2 | a0003c0003t0001g0147a0003c0003t0001g0312 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1464+2258A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302458 | ||||||
| chr9:70302466
|
C | G | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1464+2266C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302466 | ||||||
| chr9:70302494
|
G | GA | 12 | a0001c0001t0002g0008a0001c0001t0002g0125a0001c0001t0002g0126others(9): Show | 13 | HG00544.hp1 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1464+2303dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302494 | |||||
| chr9:70302494
|
G | GAA | 20 | a0002c0002t0001g0004a0002c0002t0001g0031a0002c0002t0001g0034others(17): Show | 21 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1464+2302_1464+230 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302494 | |||||
| chr9:70302494
|
G | GAAA | 35 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(32): Show | 37 | HG00140.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1464+2301_1464+230 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302494 | |||||
| chr9:70302502
|
A | AAAT | 13 | a0004c0004t0001g0320a0004c0004t0001g0335a0004c0004t0001g0337others(10): Show | 13 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1464+2303_1464+230 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302502 | |||||
| chr9:70302502
|
A | AAT | 47 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0025others(44): Show | 50 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1464+2318_1464+231 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302502 | |||||
| chr9:70302504
|
T | A | 206 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(203): Show | 217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1464+2304T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302504 | ||||||
| chr9:70302506
|
T | A | 50 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0110others(47): Show | 52 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1464+2306T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302506 | ||||||
| chr9:70302732
|
C | G | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1465-2515C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302732 | ||||||
| chr9:70302813
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465-2434A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302813 | ||||||
| chr9:70302894
|
T | G | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1465-2353T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302894 | ||||||
| chr9:70303237
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465-2010A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303237 | ||||||
| chr9:70303247
|
A | C | 9 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(6): Show | 9 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1465-2000A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303247 | ||||||
| chr9:70303249
|
AAT | A | 6 | a0001c0001t0002g0295a0005c0007t0002g0015a0005c0007t0002g0279others(3): Show | 7 | HG01358.hp2 HG01891.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-1996_1465-199 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70303249 | |||||
| chr9:70303251
|
T | C | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 112 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1465-1996T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303251 | ||||||
| chr9:70303301
|
CTATAAT | C | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1465-1941_1465-193 others(10): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70303301 | |||||
| chr9:70303307
|
T | C | 286 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(283): Show | 300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1465-1940T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303307 | ||||||
| chr9:70303310
|
T | C | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1465-1937T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303310 | ||||||
| chr9:70303319
|
T | A | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465-1928T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303319 | ||||||
| chr9:70303341
|
C | A | 1 | a0001c0001t0002g0249 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1465-1906C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303341 | ||||||
| chr9:70303447
|
C | G | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1465-1800C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303447 | ||||||
| chr9:70303457
|
G | A | 1 | a0004c0004t0001g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1465-1790G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303457 | ||||||
| chr9:70303671
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1465-1576C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303671 | ||||||
| chr9:70303692
|
A | G | 1 | a0002c0002t0001g0315 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1465-1555A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303692 | ||||||
| chr9:70303918
|
A | C | 1 | a0002c0002t0001g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1465-1329A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303918 | ||||||
| chr9:70303975
|
T | C | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1465-1272T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303975 | ||||||
| chr9:70304115
|
G | T | 1 | a0003c0003t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1465-1132G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304115 | ||||||
| chr9:70304178
|
T | A | 1 | a0003c0003t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1465-1069T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304178 | ||||||
| chr9:70304300
|
A | G | 4 | a0002c0002t0001g0025a0002c0002t0001g0026a0006c0011t0009g0310others(1): Show | 4 | HG02895.hp1 HG02897.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-947A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304300 | ||||||
| chr9:70304413
|
A | G | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1465-834A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304413 | ||||||
| chr9:70304558
|
A | T | 1 | a0001c0010t0002g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1465-689A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304558 | ||||||
| chr9:70304611
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1465-636C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304611 | ||||||
| chr9:70304718
|
C | A | 32 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(29): Show | 34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.1465-529C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304718 | ||||||
| chr9:70304752
|
G | T | 1 | a0001c0001t0002g0299 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1465-495G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304752 | ||||||
| chr9:70304796
|
G | GT | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1465-440dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70304796 | |||||
| chr9:70305134
|
A | G | 1 | a0004c0004t0001g0339 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1465-113A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70305134 | ||||||
| chr9:70305159
|
A | G | 3 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0288 | 3 | NA18961.hp1 NA18994.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1465-88A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70305159 | ||||||
| chr9:70305707
|
C | T | 1 | a0002c0002t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1578+347C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70305707 | ||||||
| chr9:70305764
|
T | C | 2 | a0003c0003t0001g0147a0003c0003t0001g0312 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1578+404T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70305764 | ||||||
| chr9:70305808
|
A | G | 57 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(54): Show | 59 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1578+448A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70305808 | ||||||
| chr9:70306102
|
T | G | 1 | a0004c0006t0001g0331 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1578+742T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306102 | ||||||
| chr9:70306121
|
A | G | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1578+761A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306121 | ||||||
| chr9:70306129
|
A | G | 2 | a0003c0003t0001g0152a0004c0004t0001g0339 | 2 | HG01106.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1578+769A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306129 | ||||||
| chr9:70306458
|
A | G | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1578+1098A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306458 | ||||||
| chr9:70306564
|
G | T | 1 | a0003c0003t0001g0202 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1578+1204G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306564 | ||||||
| chr9:70307117
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+1757G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307117 | ||||||
| chr9:70307147
|
C | T | 1 | a0002c0002t0001g0089 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1578+1787C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307147 | ||||||
| chr9:70307221
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+1861T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307221 | ||||||
| chr9:70307251
|
G | A | 5 | a0005c0007t0002g0015a0005c0007t0002g0279a0005c0007t0002g0280others(2): Show | 6 | HG01358.hp2 HG02630.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578+1891G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307251 | ||||||
| chr9:70307361
|
A | G | 1 | a0003c0003t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1578+2001A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307361 | ||||||
| chr9:70307382
|
A | C | 2 | a0002c0002t0001g0079a0002c0002t0001g0083 | 2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1578+2022A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307382 | ||||||
| chr9:70307399
|
T | C | 1 | a0002c0002t0001g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1578+2039T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307399 | ||||||
| chr9:70307433
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+2073C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307433 | ||||||
| chr9:70307550
|
T | C | 1 | a0002c0002t0001g0071 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1578+2190T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307550 | ||||||
| chr9:70307585
|
C | T | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1578+2225C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307585 | ||||||
| chr9:70307603
|
A | G | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1578+2243A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307603 | ||||||
| chr9:70307628
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1578+2268G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307628 | ||||||
| chr9:70307799
|
C | T | 1 | a0002c0002t0001g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1578+2439C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307799 | ||||||
| chr9:70307803
|
C | T | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+2443C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307803 | ||||||
| chr9:70307809
|
A | G | 10 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0128others(7): Show | 10 | HG00323.hp2 HG00408.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1578+2449A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307809 | ||||||
| chr9:70308006
|
T | A | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1578+2646T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308006 | ||||||
| chr9:70308095
|
G | A | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1578+2735G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308095 | ||||||
| chr9:70308250
|
C | G | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+2890C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308250 | ||||||
| chr9:70308274
|
T | C | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1578+2914T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308274 | ||||||
| chr9:70308332
|
G | A | 1 | a0009c0019t0003g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1578+2972G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308332 | ||||||
| chr9:70308334
|
G | A | 4 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+2974G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308334 | ||||||
| chr9:70308399
|
T | A | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1578+3039T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308399 | ||||||
| chr9:70308409
|
C | T | 7 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(4): Show | 7 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+3049C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308409 | ||||||
| chr9:70308590
|
C | CA | 12 | a0001c0001t0002g0128a0001c0001t0002g0135a0001c0001t0002g0136others(9): Show | 12 | HG01358.hp2 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1578+3259dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | |||||
| chr9:70308590
|
CA | C | 134 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(131): Show | 145 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1578+3259delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | |||||
| chr9:70308590
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0009t0014g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1578+3250_1578+325 others(14): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | |||||
| chr9:70308590
|
CAAAAAAA others(4): Show |
C | 6 | a0002c0002t0001g0048a0002c0009t0006g0095a0002c0009t0006g0098others(3): Show | 6 | HG01891.hp2 HG02056.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+3249_1578+325 others(15): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | |||||
| chr9:70308590
|
CAAAAAAA others(5): Show |
C | 112 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(109): Show | 118 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1578+3248_1578+325 others(16): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | |||||
| chr9:70308619
|
A | G | 1 | a0002c0002t0001g0038 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1578+3259A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308619 | ||||||
| chr9:70308662
|
G | A | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1578+3302G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308662 | ||||||
| chr9:70308687
|
T | G | 1 | a0002c0002t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1578+3327T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308687 | ||||||
| chr9:70308702
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+3342T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308702 | ||||||
| chr9:70309016
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1578+3656G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309016 | ||||||
| chr9:70309219
|
A | C | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1578+3859A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309219 | ||||||
| chr9:70309248
|
C | A | 1 | a0001c0001t0002g0117 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1578+3888C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309248 | ||||||
| chr9:70309250
|
T | C | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+3890T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309250 | ||||||
| chr9:70309318
|
C | CTT | 7 | a0001c0001t0002g0212a0001c0001t0002g0242a0001c0001t0002g0255others(4): Show | 7 | HG01070.hp1 HG02622.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+3988_1578+398 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
C | CTTTT | 7 | a0001c0001t0002g0215a0001c0001t0002g0248a0001c0001t0002g0249others(4): Show | 7 | HG00544.hp2 HG00609.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+3986_1578+398 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
C | CTTTTT | 40 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0203others(37): Show | 43 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1578+3985_1578+398 others(9): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
C | CTTTTTT | 32 | a0001c0001t0002g0001a0001c0001t0002g0120a0001c0001t0002g0204others(29): Show | 35 | HG00408.hp2 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1578+3984_1578+398 others(10): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
C | CTTTTTTT | 7 | a0001c0001t0002g0205a0001c0001t0002g0245a0001c0001t0002g0246others(4): Show | 7 | HG00438.hp1 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+3983_1578+398 others(11): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0230 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1578+3980_1578+398 others(14): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
C | CTTTTTTT others(5): Show |
1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1578+3978_1578+398 others(16): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CT | C | 9 | a0001c0001t0002g0208a0001c0001t0002g0211a0001c0005t0003g0019others(6): Show | 10 | HG01884.hp1 HG02080.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1578+3989delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTT | C | 25 | a0001c0001t0002g0271a0001c0005t0003g0018a0001c0005t0003g0020others(22): Show | 25 | HG00673.hp2 HG00738.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1578+3988_1578+398 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTT | C | 35 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(32): Show | 37 | HG00741.hp1 HG01256.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.1578+3987_1578+398 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTTT | C | 21 | a0002c0002t0001g0077a0003c0003t0001g0003a0003c0003t0001g0010others(18): Show | 24 | HG00609.hp1 HG01255.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1578+3986_1578+398 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTTTT | C | 16 | a0003c0003t0001g0106a0003c0003t0001g0151a0003c0003t0001g0174others(13): Show | 16 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1578+3985_1578+398 others(9): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTTTTTT others(3): Show |
C | 1 | a0004c0004t0001g0337 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1578+3980_1578+398 others(14): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTTTTTT others(4): Show |
C | 23 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(20): Show | 23 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1578+3979_1578+398 others(15): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0002g0011a0001c0001t0002g0225a0001c0001t0002g0302others(2): Show | 6 | NA18747.hp1 NA18949.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+3978_1578+398 others(16): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTTTTTT others(6): Show |
C | 56 | a0001c0001t0002g0224a0001c0001t0002g0226a0001c0001t0002g0285others(53): Show | 60 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1578+3977_1578+398 others(17): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0002g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1578+3976_1578+398 others(18): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309318
|
CTTTTTTT others(8): Show |
C | 24 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0122others(21): Show | 25 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1578+3975_1578+398 others(19): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | |||||
| chr9:70309330
|
TTTTTTTT others(13): Show |
T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+3971_1578+399 others(24): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309330 | ||||||
| chr9:70309349
|
T | G | 4 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027others(1): Show | 4 | HG00597.hp2 NA18947.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+3989T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309349 | ||||||
| chr9:70309349
|
T | TTTTTTTT others(13): Show |
1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1578+3989_1578+399 others(24): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309349 | ||||||
| chr9:70309373
|
C | T | 2 | a0001c0005t0003g0023a0001c0005t0003g0024 | 2 | HG01496.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1578+4013C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309373 | ||||||
| chr9:70309589
|
T | G | 58 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0119others(55): Show | 61 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1578+4229T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309589 | ||||||
| chr9:70309872
|
C | G | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1578+4512C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309872 | ||||||
| chr9:70310192
|
C | T | 1 | a0015c0020t0006g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1579-4550C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310192 | ||||||
| chr9:70310200
|
G | A | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579-4542G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310200 | ||||||
| chr9:70310381
|
CAGTG | C | 25 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(22): Show | 27 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1579-4358_1579-435 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70310381 | |||||
| chr9:70310475
|
G | C | 1 | a0001c0001t0002g0118 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1579-4267G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310475 | ||||||
| chr9:70310602
|
A | G | 1 | a0002c0002t0001g0315 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1579-4140A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310602 | ||||||
| chr9:70310666
|
T | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-4076T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310666 | ||||||
| chr9:70310731
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-4011G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310731 | ||||||
| chr9:70310761
|
T | C | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-3981T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310761 | ||||||
| chr9:70310763
|
CATCAG | C | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-3978_1579-397 others(9): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310763 | ||||||
| chr9:70310782
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-3960A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310782 | ||||||
| chr9:70310985
|
T | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-3757T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310985 | ||||||
| chr9:70311470
|
A | C | 1 | a0002c0002t0001g0047 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1579-3272A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70311470 | ||||||
| chr9:70311701
|
CA | C | 14 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(11): Show | 14 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1579-3026delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70311701 | |||||
| chr9:70311959
|
A | T | 1 | a0001c0001t0002g0248 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1579-2783A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70311959 | ||||||
| chr9:70311992
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-2750G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70311992 | ||||||
| chr9:70312075
|
C | T | 1 | a0003c0003t0001g0202 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1579-2667C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312075 | ||||||
| chr9:70312120
|
C | CA | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579-2594dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | |||||
| chr9:70312120
|
CA | C | 34 | a0001c0001t0002g0125a0001c0001t0002g0203a0001c0001t0002g0209others(31): Show | 34 | HG00609.hp2 HG00735.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.1579-2594delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | |||||
| chr9:70312120
|
CAA | C | 197 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(194): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1579-2595_1579-259 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | |||||
| chr9:70312120
|
CAAA | C | 72 | a0001c0001t0002g0302a0001c0001t0002g0307a0001c0001t0007g0293others(69): Show | 76 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1579-2596_1579-259 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | |||||
| chr9:70312120
|
CAAAA | C | 25 | a0002c0002t0001g0006a0002c0002t0001g0072a0002c0002t0001g0073others(22): Show | 27 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1579-2597_1579-259 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | |||||
| chr9:70312299
|
G | A | 1 | a0002c0002t0001g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1579-2443G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312299 | ||||||
| chr9:70312315
|
C | T | 1 | a0001c0005t0003g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1579-2427C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312315 | ||||||
| chr9:70312560
|
C | T | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1579-2182C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312560 | ||||||
| chr9:70312631
|
T | A | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-2111T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312631 | ||||||
| chr9:70312677
|
A | T | 11 | a0001c0001t0002g0011a0001c0001t0002g0225a0001c0001t0002g0227others(8): Show | 12 | HG01099.hp2 HG01261.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579-2065A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312677 | ||||||
| chr9:70312781
|
C | T | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1579-1961C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312781 | ||||||
| chr9:70313078
|
G | T | 1 | a0012c0014t0001g0065 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1579-1664G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313078 | ||||||
| chr9:70313250
|
A | T | 25 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0122others(22): Show | 26 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1579-1492A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313250 | ||||||
| chr9:70313352
|
C | T | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1579-1390C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313352 | ||||||
| chr9:70313466
|
T | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-1276T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313466 | ||||||
| chr9:70313470
|
G | A | 1 | a0003c0003t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1579-1272G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313470 | ||||||
| chr9:70313569
|
C | G | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-1173C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313569 | ||||||
| chr9:70313603
|
T | C | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579-1139T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313603 | ||||||
| chr9:70313796
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-946A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313796 | ||||||
| chr9:70313887
|
T | C | 7 | a0003c0003t0001g0174a0003c0003t0001g0176a0003c0003t0001g0177others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1579-855T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313887 | ||||||
| chr9:70313937
|
G | T | 1 | a0001c0001t0002g0276 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1579-805G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313937 | ||||||
| chr9:70314118
|
CCTT | C | 3 | a0004c0004t0001g0325a0004c0004t0001g0329a0004c0004t0001g0330 | 3 | HG01070.hp2 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1579-619_1579-617d others(5): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70314118 | |||||
| chr9:70314183
|
A | G | 24 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(21): Show | 24 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1579-559A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314183 | ||||||
| chr9:70314207
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1579-535A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314207 | ||||||
| chr9:70314310
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-432A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314310 | ||||||
| chr9:70314364
|
C | G | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1579-378C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314364 | ||||||
| chr9:70314377
|
G | T | 2 | a0004c0004t0001g0344a0013c0015t0011g0108 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1579-365G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314377 | ||||||
| chr9:70314467
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-275A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314467 | ||||||
| chr9:70314493
|
A | C | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1579-249A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314493 | ||||||
| chr9:70314495
|
T | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-247T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314495 | ||||||
| chr9:70314587
|
T | C | 106 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(103): Show | 114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1579-155T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314587 | ||||||
| chr9:70314849
|
A | C | 1 | a0001c0001t0002g0305 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1673+13A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | chr9 | 70314849 | ||||||
| chr9:70314852
|
A | G | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1673+16A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | chr9 | 70314852 | ||||||
| chr9:70314853
|
C | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1673+17C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | chr9 | 70314853 | ||||||
| chr9:70315308
|
T | TAAAA | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1674-137_1674-134d others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr9 | 70315308 | |||||
| chr9:70315428
|
C | T | 1 | a0001c0005t0003g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1674-18C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | chr9 | 70315428 | ||||||
| chr9:70315931
|
T | C | 1 | a0001c0001t0002g0215 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1806+353T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70315931 | ||||||
| chr9:70316082
|
G | T | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1806+504G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316082 | ||||||
| chr9:70316275
|
G | A | 24 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(21): Show | 24 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1806+697G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316275 | ||||||
| chr9:70316317
|
A | T | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1806+739A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316317 | ||||||
| chr9:70316385
|
A | G | 2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1806+807A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316385 | ||||||
| chr9:70316451
|
CTTAACAG others(6): Show |
C | 7 | a0003c0003t0001g0174a0003c0003t0001g0176a0003c0003t0001g0177others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1806+874_1806+886d others(15): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316451 | ||||||
| chr9:70316453
|
TA | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1806+877delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 70316453 | |||||
| chr9:70316582
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1806+1004A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316582 | ||||||
| chr9:70317165
|
T | A | 1 | a0003c0003t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1807-1349T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317165 | ||||||
| chr9:70317233
|
A | G | 21 | a0001c0001t0002g0001a0001c0001t0002g0215a0001c0001t0002g0224others(18): Show | 24 | HG00408.hp2 HG00735.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1807-1281A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317233 | ||||||
| chr9:70317245
|
C | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1807-1269C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317245 | ||||||
| chr9:70317260
|
T | G | 8 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0255others(5): Show | 8 | HG02486.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1807-1254T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317260 | ||||||
| chr9:70317295
|
C | T | 1 | a0002c0002t0001g0052 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1807-1219C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317295 | ||||||
| chr9:70317528
|
T | C | 1 | a0003c0003t0001g0202 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1807-986T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317528 | ||||||
| chr9:70317838
|
T | G | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1807-676T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317838 | ||||||
| chr9:70317952
|
A | ACTCTTCT others(10): Show |
55 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(52): Show | 57 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.1807-549_1807-548i others(19): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 70317952 | |||||
| chr9:70317966
|
C | G | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1807-548C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317966 | ||||||
| chr9:70318023
|
G | A | 1 | a0002c0002t0001g0318 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1807-491G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318023 | ||||||
| chr9:70318149
|
C | G | 1 | a0001c0005t0003g0022 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1807-365C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318149 | ||||||
| chr9:70318292
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1807-222G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318292 | ||||||
| chr9:70318305
|
T | C | 60 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0106others(57): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1807-209T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318305 | ||||||
| chr9:70318343
|
G | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1807-171G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318343 | ||||||
| chr9:70318357
|
C | G | 1 | a0001c0001t0002g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1807-157C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318357 | ||||||
| chr9:70318361
|
C | G | 2 | a0003c0003t0001g0147a0003c0003t0001g0312 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1807-153C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318361 | ||||||
| chr9:70318983
|
G | C | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2150+20G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70318983 | ||||||
| chr9:70319042
|
G | C | 339 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(336): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2150+79G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319042 | ||||||
| chr9:70319082
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2150+119C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319082 | ||||||
| chr9:70319114
|
T | C | 1 | a0003c0003t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2150+151T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319114 | ||||||
| chr9:70319174
|
T | C | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2150+211T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319174 | ||||||
| chr9:70319278
|
T | C | 1 | a0003c0003t0001g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2150+315T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319278 | ||||||
| chr9:70319448
|
A | T | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2150+485A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319448 | ||||||
| chr9:70319713
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2150+750C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319713 | ||||||
| chr9:70319795
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2150+832A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319795 | ||||||
| chr9:70320287
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2150+1324A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70320287 | ||||||
| chr9:70320403
|
G | A | 4 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150+1440G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70320403 | ||||||
| chr9:70320514
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2150+1551A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70320514 | ||||||
| chr9:70320561
|
A | G | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150+1598A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70320561 | ||||||
| chr9:70321082
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2150+2119G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321082 | ||||||
| chr9:70321153
|
G | A | 1 | a0002c0002t0001g0318 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2150+2190G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321153 | ||||||
| chr9:70321155
|
A | G | 346 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(343): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2150+2192A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321155 | ||||||
| chr9:70321236
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2151-2247T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321236 | ||||||
| chr9:70321248
|
C | T | 2 | a0001c0001t0002g0237a0001c0001t0002g0248 | 2 | NA18972.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2151-2235C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321248 | ||||||
| chr9:70321252
|
A | G | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-2231A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321252 | ||||||
| chr9:70321392
|
G | A | 3 | a0001c0001t0002g0232a0001c0001t0002g0239a0004c0006t0001g0342 | 3 | HG02129.hp1 HG02809.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2151-2091G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321392 | ||||||
| chr9:70321394
|
C | CT | 65 | a0001c0001t0002g0212a0001c0001t0002g0248a0001c0001t0002g0254others(62): Show | 67 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2151-2073dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70321394 | |||||
| chr9:70321394
|
C | CTT | 54 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(51): Show | 58 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2151-2074_2151-207 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70321394 | |||||
| chr9:70321414
|
A | G | 1 | a0004c0004t0001g0334 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2151-2069A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321414 | ||||||
| chr9:70321429
|
GT | G | 112 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(109): Show | 120 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2151-2052delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70321429 | |||||
| chr9:70321647
|
G | A | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2151-1836G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321647 | ||||||
| chr9:70321826
|
A | C | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2151-1657A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321826 | ||||||
| chr9:70321901
|
TTTG | T | 64 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142others(61): Show | 66 | HG00140.hp2 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2151-1567_2151-156 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70321901 | |||||
| chr9:70321933
|
A | G | 6 | a0002c0002t0001g0004a0002c0002t0001g0031a0002c0002t0001g0032others(3): Show | 7 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2151-1550A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321933 | ||||||
| chr9:70321969
|
A | T | 1 | a0001c0001t0002g0133 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2151-1514A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321969 | ||||||
| chr9:70322103
|
T | C | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2151-1380T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322103 | ||||||
| chr9:70322183
|
CTATT | C | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2151-1297_2151-129 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70322183 | |||||
| chr9:70322345
|
G | C | 1 | a0002c0002t0001g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2151-1138G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322345 | ||||||
| chr9:70322426
|
A | C | 4 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(1): Show | 4 | NA18950.hp2 NA18995.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.2151-1057A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322426 | ||||||
| chr9:70322522
|
G | A | 1 | a0004c0004t0001g0334 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2151-961G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322522 | ||||||
| chr9:70322573
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2151-910C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322573 | ||||||
| chr9:70322641
|
GCCTGGCC others(13): Show |
G | 4 | a0001c0001t0002g0292a0001c0001t0007g0290a0001c0001t0007g0291others(1): Show | 4 | HG00738.hp1 HG01070.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2151-837_2151-818d others(22): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70322641 | |||||
| chr9:70322665
|
G | C | 1 | a0001c0001t0002g0272 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2151-818G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322665 | ||||||
| chr9:70322837
|
A | G | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-646A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322837 | ||||||
| chr9:70322909
|
C | T | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2151-574C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322909 | ||||||
| chr9:70322915
|
T | C | 4 | a0001c0001t0002g0122a0001c0001t0002g0129a0001c0001t0002g0130others(1): Show | 4 | HG00408.hp1 NA18612.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2151-568T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322915 | ||||||
| chr9:70322985
|
C | G | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2151-498C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322985 | ||||||
| chr9:70322986
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2151-497G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322986 | ||||||
| chr9:70323022
|
G | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2151-461G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70323022 | ||||||
| chr9:70323337
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2151-146T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70323337 | ||||||
| chr9:70323612
|
G | A | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2274+6G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 16/24 | chr9 | 70323612 | ||||||
| chr9:70323782
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2274+176G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 16/24 | chr9 | 70323782 | ||||||
| chr9:70323962
|
T | G | 1 | a0003c0003t0001g0191 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2275-59T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 16/24 | chr9 | 70323962 | ||||||
| chr9:70324157
|
C | G | 3 | a0003c0003t0001g0174a0003c0003t0001g0177a0003c0003t0001g0199 | 3 | HG00099.hp1 HG00323.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2397+14C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324157 | ||||||
| chr9:70324209
|
C | T | 4 | a0004c0008t0005g0101a0004c0008t0005g0102a0004c0008t0005g0103others(1): Show | 4 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397+66C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324209 | ||||||
| chr9:70324279
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2397+136G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324279 | ||||||
| chr9:70324394
|
A | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+251A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324394 | ||||||
| chr9:70324487
|
T | C | 339 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(336): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2397+344T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324487 | ||||||
| chr9:70324519
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+376A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324519 | ||||||
| chr9:70324767
|
C | T | 1 | a0004c0004t0018g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2397+624C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324767 | ||||||
| chr9:70324786
|
C | T | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2397+643C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324786 | ||||||
| chr9:70324884
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+741T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324884 | ||||||
| chr9:70324990
|
G | A | 125 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142others(122): Show | 131 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2397+847G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324990 | ||||||
| chr9:70325169
|
G | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+1026G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325169 | ||||||
| chr9:70325236
|
G | A | 1 | a0015c0020t0006g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2397+1093G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325236 | ||||||
| chr9:70325249
|
T | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+1106T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325249 | ||||||
| chr9:70325253
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2397+1110C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325253 | ||||||
| chr9:70325348
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+1205G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325348 | ||||||
| chr9:70325381
|
A | G | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2397+1238A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325381 | ||||||
| chr9:70325381
|
A | T | 2 | a0001c0001t0002g0121a0001c0001t0002g0127 | 2 | HG02055.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2397+1238A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325381 | ||||||
| chr9:70325579
|
T | A | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2397+1436T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325579 | ||||||
| chr9:70325670
|
T | C | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2397+1527T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325670 | ||||||
| chr9:70325818
|
A | G | 2 | a0004c0004t0001g0324a0004c0004t0001g0343 | 2 | NA18955.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2397+1675A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325818 | ||||||
| chr9:70326054
|
A | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0272a0001c0001t0002g0289 | 4 | HG01257.hp2 HG01975.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.2397+1911A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326054 | ||||||
| chr9:70326384
|
G | A | 1 | a0002c0002t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2397+2241G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326384 | ||||||
| chr9:70326596
|
CT | C | 44 | a0001c0001t0002g0122a0001c0001t0002g0126a0001c0001t0002g0131others(41): Show | 46 | HG00609.hp1 HG00673.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2397+2469delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70326596 | |||||
| chr9:70326650
|
G | A | 2 | a0001c0001t0002g0215a0001c0001t0015g0266 | 2 | NA18944.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2397+2507G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326650 | ||||||
| chr9:70326818
|
T | G | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2397+2675T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326818 | ||||||
| chr9:70326851
|
C | T | 6 | a0001c0001t0002g0295a0005c0007t0002g0015a0005c0007t0002g0279others(3): Show | 7 | HG01358.hp2 HG01891.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2397+2708C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326851 | ||||||
| chr9:70326889
|
G | A | 2 | a0003c0003t0001g0147a0003c0003t0001g0312 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2397+2746G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326889 | ||||||
| chr9:70327037
|
T | C | 1 | a0002c0002t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2397+2894T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327037 | ||||||
| chr9:70327080
|
A | G | 61 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0105others(58): Show | 65 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2397+2937A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327080 | ||||||
| chr9:70327090
|
T | G | 3 | a0002c0002t0001g0112a0002c0002t0001g0114a0002c0002t0001g0315 | 3 | NA18940.hp1 NA19006.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2397+2947T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327090 | ||||||
| chr9:70327231
|
C | T | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2397+3088C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327231 | ||||||
| chr9:70327320
|
A | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2397+3177A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327320 | ||||||
| chr9:70327582
|
A | G | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+3439A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327582 | ||||||
| chr9:70327628
|
A | G | 1 | a0002c0002t0001g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2397+3485A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327628 | ||||||
| chr9:70327828
|
G | T | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2397+3685G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327828 | ||||||
| chr9:70327897
|
G | A | 3 | a0004c0004t0001g0321a0004c0004t0001g0322a0004c0004t0001g0323 | 3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2397+3754G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327897 | ||||||
| chr9:70327944
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2397+3801G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327944 | ||||||
| chr9:70328019
|
C | T | 26 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(23): Show | 26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.2397+3876C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328019 | ||||||
| chr9:70328140
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2397+3997C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328140 | ||||||
| chr9:70328183
|
C | T | 1 | a0004c0004t0018g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2397+4040C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328183 | ||||||
| chr9:70328185
|
A | T | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+4042A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328185 | ||||||
| chr9:70328373
|
C | T | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2397+4230C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328373 | ||||||
| chr9:70328434
|
A | G | 3 | a0003c0003t0001g0153a0003c0003t0001g0155a0003c0003t0001g0201 | 3 | HG01496.hp2 HG02300.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2397+4291A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328434 | ||||||
| chr9:70328543
|
T | C | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2397+4400T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328543 | ||||||
| chr9:70328596
|
C | T | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+4453C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328596 | ||||||
| chr9:70328655
|
G | A | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2397+4512G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328655 | ||||||
| chr9:70328808
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2397+4665G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328808 | ||||||
| chr9:70328861
|
C | T | 15 | a0003c0003t0001g0010a0003c0003t0001g0145a0003c0003t0001g0152others(12): Show | 16 | HG01496.hp2 HG02083.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2397+4718C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328861 | ||||||
| chr9:70328998
|
C | T | 6 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210others(3): Show | 6 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2397+4855C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328998 | ||||||
| chr9:70329000
|
T | G | 5 | a0003c0003t0001g0178a0003c0003t0001g0186a0003c0003t0001g0187others(2): Show | 5 | NA18945.hp2 NA18961.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+4857T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329000 | ||||||
| chr9:70329012
|
C | T | 1 | a0015c0020t0006g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2397+4869C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329012 | ||||||
| chr9:70329044
|
A | C | 1 | a0004c0008t0005g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2397+4901A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329044 | ||||||
| chr9:70329082
|
A | G | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2397+4939A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329082 | ||||||
| chr9:70329115
|
T | A | 1 | a0001c0001t0002g0105 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2397+4972T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329115 | ||||||
| chr9:70329412
|
G | A | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2397+5269G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329412 | ||||||
| chr9:70329486
|
C | T | 58 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0119others(55): Show | 61 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2397+5343C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329486 | ||||||
| chr9:70329499
|
G | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+5356G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329499 | ||||||
| chr9:70329510
|
G | A | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2397+5367G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329510 | ||||||
| chr9:70329526
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2397+5383A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329526 | ||||||
| chr9:70329628
|
C | G | 1 | a0001c0001t0002g0270 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2397+5485C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329628 | ||||||
| chr9:70329882
|
G | T | 60 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0106others(57): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2397+5739G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329882 | ||||||
| chr9:70329944
|
G | T | 1 | a0003c0003t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2397+5801G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329944 | ||||||
| chr9:70330038
|
A | C | 1 | a0001c0005t0003g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2397+5895A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330038 | ||||||
| chr9:70330076
|
T | C | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2397+5933T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330076 | ||||||
| chr9:70330145
|
A | T | 1 | a0003c0003t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2397+6002A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330145 | ||||||
| chr9:70330286
|
T | C | 1 | a0001c0001t0002g0299 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2397+6143T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330286 | ||||||
| chr9:70330548
|
C | CT | 63 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0105others(60): Show | 67 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2397+6423dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70330548 | |||||
| chr9:70330548
|
CT | C | 115 | a0001c0001t0002g0131a0001c0001t0002g0217a0001c0001t0007g0290others(112): Show | 121 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2397+6423delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70330548 | |||||
| chr9:70330548
|
CTT | C | 7 | a0002c0002t0001g0028a0002c0002t0004g0085a0002c0009t0006g0095others(4): Show | 7 | HG01070.hp2 HG01891.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2397+6422_2397+642 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70330548 | |||||
| chr9:70330567
|
C | T | 1 | a0001c0005t0003g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2397+6424C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330567 | ||||||
| chr9:70330568
|
A | C | 1 | a0001c0005t0003g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2397+6425A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330568 | ||||||
| chr9:70330646
|
G | A | 1 | a0002c0002t0001g0041 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2397+6503G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330646 | ||||||
| chr9:70330657
|
C | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+6514C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330657 | ||||||
| chr9:70331095
|
G | A | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2397+6952G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331095 | ||||||
| chr9:70331175
|
T | A | 5 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+7032T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331175 | ||||||
| chr9:70331241
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2397+7098T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331241 | ||||||
| chr9:70331413
|
A | T | 38 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.2397+7270A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331413 | ||||||
| chr9:70331415
|
AAAAC | A | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2397+7274_2397+727 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70331415 | |||||
| chr9:70331419
|
CAG | C | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+7277_2397+727 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331419 | ||||||
| chr9:70331471
|
G | A | 338 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(335): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2397+7328G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331471 | ||||||
| chr9:70331471
|
G | T | 1 | a0001c0005t0003g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2397+7328G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331471 | ||||||
| chr9:70331495
|
A | G | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2397+7352A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331495 | ||||||
| chr9:70331505
|
G | GT | 122 | a0001c0001t0002g0288a0002c0002t0001g0002a0002c0002t0001g0004others(119): Show | 128 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2397+7372dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70331505 | |||||
| chr9:70331519
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+7376C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331519 | ||||||
| chr9:70331777
|
G | A | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+7634G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331777 | ||||||
| chr9:70331941
|
G | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+7798G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331941 | ||||||
| chr9:70331960
|
C | T | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2397+7817C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331960 | ||||||
| chr9:70332045
|
T | C | 1 | a0003c0003t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2397+7902T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332045 | ||||||
| chr9:70332101
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2397+7958C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332101 | ||||||
| chr9:70332156
|
C | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+8013C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332156 | ||||||
| chr9:70332227
|
A | G | 2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2397+8084A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332227 | ||||||
| chr9:70332232
|
A | G | 1 | a0005c0007t0002g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2397+8089A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332232 | ||||||
| chr9:70332523
|
C | CA | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(54): Show | 61 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.2397+8401dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332523 | |||||
| chr9:70332523
|
C | CAA | 7 | a0002c0002t0001g0038a0002c0002t0001g0042a0002c0002t0001g0070others(4): Show | 7 | HG01891.hp2 HG02080.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2397+8400_2397+840 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332523 | |||||
| chr9:70332523
|
CA | C | 66 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0122others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.2397+8401delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332523 | |||||
| chr9:70332523
|
CAA | C | 126 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(123): Show | 134 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.2397+8400_2397+840 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332523 | |||||
| chr9:70332660
|
C | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+8517C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332660 | ||||||
| chr9:70332691
|
T | C | 1 | a0004c0004t0001g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2397+8548T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332691 | ||||||
| chr9:70332828
|
C | CTGA | 32 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(29): Show | 34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2397+8686_2397+868 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332828 | |||||
| chr9:70332918
|
C | T | 2 | a0001c0001t0002g0122a0001c0001t0002g0130 | 2 | HG00408.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2397+8775C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332918 | ||||||
| chr9:70332994
|
A | T | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2397+8851A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332994 | ||||||
| chr9:70333055
|
G | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+8912G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333055 | ||||||
| chr9:70333110
|
T | TA | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2397+8976dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70333110 | |||||
| chr9:70333113
|
A | G | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.2397+8970A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333113 | ||||||
| chr9:70333290
|
A | G | 1 | a0002c0002t0001g0047 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2397+9147A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333290 | ||||||
| chr9:70333303
|
G | C | 4 | a0001c0001t0002g0304a0001c0001t0002g0306a0001c0001t0002g0307others(1): Show | 4 | HG00544.hp2 NA18965.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2397+9160G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333303 | ||||||
| chr9:70333468
|
G | T | 1 | a0002c0002t0001g0043 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2397+9325G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333468 | ||||||
| chr9:70333470
|
C | T | 1 | a0002c0002t0001g0043 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2397+9327C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333470 | ||||||
| chr9:70333583
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2397+9440T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333583 | ||||||
| chr9:70333601
|
C | T | 1 | a0001c0010t0002g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2397+9458C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333601 | ||||||
| chr9:70333641
|
G | T | 2 | a0001c0005t0003g0023a0001c0005t0003g0024 | 2 | HG01496.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2397+9498G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333641 | ||||||
| chr9:70333749
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2397+9606A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333749 | ||||||
| chr9:70333791
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+9648C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333791 | ||||||
| chr9:70333828
|
T | A | 5 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+9685T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333828 | ||||||
| chr9:70333893
|
T | TG | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.2397+9750_2397+975 others(5): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333893 | ||||||
| chr9:70334037
|
AGACATTG others(21): Show |
A | 1 | a0004c0004t0001g0343 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2397+9895_2397+992 others(32): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334037 | ||||||
| chr9:70334129
|
G | GT | 47 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(44): Show | 48 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.2398-9999dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70334129 | |||||
| chr9:70334132
|
T | G | 8 | a0003c0003t0001g0106a0004c0008t0005g0100a0004c0008t0005g0101others(5): Show | 8 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2397+9989T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334132 | ||||||
| chr9:70334183
|
A | C | 32 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(29): Show | 34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2398-9961A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334183 | ||||||
| chr9:70334252
|
G | A | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2398-9892G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334252 | ||||||
| chr9:70334388
|
T | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-9756T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334388 | ||||||
| chr9:70334418
|
A | C | 4 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0081others(1): Show | 4 | HG00673.hp2 NA18967.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.2398-9726A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334418 | ||||||
| chr9:70334439
|
C | T | 1 | a0004c0004t0001g0325 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2398-9705C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334439 | ||||||
| chr9:70334557
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2398-9587A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334557 | ||||||
| chr9:70334724
|
G | T | 1 | a0003c0003t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2398-9420G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334724 | ||||||
| chr9:70334736
|
A | G | 2 | a0002c0002t0001g0030a0002c0002t0001g0038 | 2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.2398-9408A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334736 | ||||||
| chr9:70334746
|
C | T | 1 | a0001c0005t0003g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2398-9398C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334746 | ||||||
| chr9:70334752
|
A | G | 32 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(29): Show | 34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2398-9392A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334752 | ||||||
| chr9:70334868
|
C | G | 1 | a0001c0001t0002g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2398-9276C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334868 | ||||||
| chr9:70334877
|
C | A | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2398-9267C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334877 | ||||||
| chr9:70334949
|
G | A | 1 | a0003c0003t0001g0346 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2398-9195G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334949 | ||||||
| chr9:70335238
|
T | G | 25 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(22): Show | 27 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.2398-8906T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335238 | ||||||
| chr9:70335316
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2398-8828T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335316 | ||||||
| chr9:70335330
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-8814G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335330 | ||||||
| chr9:70335408
|
A | G | 345 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(342): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2398-8736A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335408 | ||||||
| chr9:70335452
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-8692G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335452 | ||||||
| chr9:70335462
|
A | G | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2398-8682A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335462 | ||||||
| chr9:70335526
|
C | T | 1 | a0002c0002t0001g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2398-8618C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335526 | ||||||
| chr9:70335536
|
T | A | 2 | a0001c0001t0002g0257a0001c0001t0002g0316 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2398-8608T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335536 | ||||||
| chr9:70335589
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2398-8555A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335589 | ||||||
| chr9:70335696
|
A | G | 1 | a0002c0002t0019g0045 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2398-8448A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335696 | ||||||
| chr9:70335713
|
A | G | 119 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(116): Show | 125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2398-8431A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335713 | ||||||
| chr9:70336207
|
TGTA | T | 31 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(28): Show | 33 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.2398-7935_2398-793 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70336207 | |||||
| chr9:70336213
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2398-7931C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336213 | ||||||
| chr9:70336501
|
A | G | 38 | a0001c0001t0002g0008a0001c0001t0002g0110a0001c0001t0002g0111others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.2398-7643A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336501 | ||||||
| chr9:70336703
|
A | G | 1 | a0001c0001t0002g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2398-7441A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336703 | ||||||
| chr9:70336855
|
A | G | 1 | a0002c0002t0022g0074 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2398-7289A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336855 | ||||||
| chr9:70336909
|
G | A | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2398-7235G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336909 | ||||||
| chr9:70336938
|
C | T | 25 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0122others(22): Show | 26 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2398-7206C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336938 | ||||||
| chr9:70337118
|
C | T | 52 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(49): Show | 54 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.2398-7026C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337118 | ||||||
| chr9:70337173
|
C | T | 1 | a0003c0003t0001g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2398-6971C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337173 | ||||||
| chr9:70337206
|
T | G | 2 | a0004c0008t0005g0101a0004c0008t0005g0104 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2398-6938T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337206 | ||||||
| chr9:70337373
|
A | G | 1 | a0001c0001t0002g0284 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2398-6771A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337373 | ||||||
| chr9:70337438
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2398-6706G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337438 | ||||||
| chr9:70337450
|
GT | G | 81 | a0001c0001t0002g0110a0001c0001t0002g0124a0001c0001t0002g0126others(78): Show | 84 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2398-6670delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | |||||
| chr9:70337450
|
GTT | G | 86 | a0001c0001t0002g0008a0001c0001t0002g0111a0001c0001t0002g0121others(83): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.2398-6671_2398-667 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | |||||
| chr9:70337450
|
GTTT | G | 27 | a0002c0002t0001g0006a0002c0002t0001g0046a0002c0002t0001g0071others(24): Show | 29 | HG00673.hp2 HG01256.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.2398-6672_2398-667 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | |||||
| chr9:70337450
|
GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0002g0242a0001c0001t0002g0264a0001c0001t0002g0295 | 3 | HG01891.hp1 NA18991.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2398-6683_2398-667 others(18): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | |||||
| chr9:70337450
|
GTTTTTTT others(8): Show |
G | 109 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 117 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.2398-6684_2398-667 others(19): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | |||||
| chr9:70337519
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-6625A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337519 | ||||||
| chr9:70337589
|
G | T | 1 | a0004c0004t0001g0326 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2398-6555G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337589 | ||||||
| chr9:70337772
|
A | T | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2398-6372A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337772 | ||||||
| chr9:70337788
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2398-6356G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337788 | ||||||
| chr9:70337814
|
T | G | 1 | a0003c0003t0008g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2398-6330T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337814 | ||||||
| chr9:70337851
|
A | AT | 182 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(179): Show | 193 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.2398-6279dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337851 | |||||
| chr9:70337851
|
A | ATT | 8 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(5): Show | 8 | HG01433.hp2 HG01928.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.2398-6280_2398-627 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337851 | |||||
| chr9:70337851
|
AT | A | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(54): Show | 61 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.2398-6279delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337851 | |||||
| chr9:70337958
|
G | A | 106 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(103): Show | 114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2398-6186G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337958 | ||||||
| chr9:70337973
|
G | T | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2398-6171G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337973 | ||||||
| chr9:70338053
|
C | T | 3 | a0003c0003t0001g0156a0003c0003t0001g0157a0003c0003t0001g0166 | 3 | NA18987.hp2 NA19055.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2398-6091C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338053 | ||||||
| chr9:70338126
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0277 | 3 | HG01928.hp2 HG02148.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2398-6018C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338126 | ||||||
| chr9:70338444
|
G | A | 26 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(23): Show | 28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.2398-5700G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338444 | ||||||
| chr9:70338568
|
A | C | 106 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(103): Show | 114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2398-5576A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338568 | ||||||
| chr9:70338576
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2398-5568A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338576 | ||||||
| chr9:70338605
|
A | G | 1 | a0001c0001t0002g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2398-5539A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338605 | ||||||
| chr9:70338752
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-5392C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338752 | ||||||
| chr9:70338836
|
A | G | 1 | a0001c0005t0003g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2398-5308A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338836 | ||||||
| chr9:70338840
|
C | T | 1 | a0004c0004t0018g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2398-5304C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338840 | ||||||
| chr9:70338843
|
T | C | 1 | a0001c0001t0016g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2398-5301T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338843 | ||||||
| chr9:70338867
|
T | A | 1 | a0002c0002t0019g0045 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2398-5277T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338867 | ||||||
| chr9:70339066
|
A | C | 2 | a0003c0003t0001g0178a0003c0003t0001g0186 | 2 | NA18961.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2398-5078A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339066 | ||||||
| chr9:70339225
|
C | T | 1 | a0010c0016t0002g0301 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2398-4919C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339225 | ||||||
| chr9:70339360
|
C | T | 150 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(147): Show | 159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2398-4784C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339360 | ||||||
| chr9:70339361
|
G | A | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2398-4783G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339361 | ||||||
| chr9:70339423
|
C | T | 1 | a0010c0016t0002g0301 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2398-4721C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339423 | ||||||
| chr9:70339662
|
A | G | 1 | a0001c0001t0021g0317 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2398-4482A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339662 | ||||||
| chr9:70339914
|
G | A | 2 | a0002c0002t0001g0091a0002c0002t0001g0092 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2398-4230G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339914 | ||||||
| chr9:70339986
|
C | CGTT | 60 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0106others(57): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2398-4158_2398-415 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339986 | ||||||
| chr9:70339987
|
C | A | 60 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0106others(57): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2398-4157C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339987 | ||||||
| chr9:70339992
|
C | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-4152C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339992 | ||||||
| chr9:70340288
|
C | CT | 32 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(29): Show | 34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2398-3846dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70340288 | |||||
| chr9:70340324
|
A | G | 1 | a0002c0002t0001g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2398-3820A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340324 | ||||||
| chr9:70340559
|
AATG | A | 25 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0122others(22): Show | 26 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2398-3581_2398-357 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70340559 | |||||
| chr9:70340727
|
T | C | 2 | a0003c0003t0001g0146a0003c0003t0001g0314 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2398-3417T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340727 | ||||||
| chr9:70340815
|
G | A | 3 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0235 | 3 | HG00642.hp1 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2398-3329G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340815 | ||||||
| chr9:70340841
|
G | C | 341 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(338): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.2398-3303G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340841 | ||||||
| chr9:70340846
|
G | A | 1 | a0011c0017t0002g0214 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2398-3298G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340846 | ||||||
| chr9:70340931
|
G | C | 2 | a0003c0003t0001g0146a0003c0003t0001g0314 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2398-3213G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340931 | ||||||
| chr9:70341027
|
G | A | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2398-3117G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341027 | ||||||
| chr9:70341135
|
G | T | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2398-3009G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341135 | ||||||
| chr9:70341174
|
G | T | 1 | a0001c0001t0002g0210 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2398-2970G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341174 | ||||||
| chr9:70341251
|
C | T | 116 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(113): Show | 122 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2398-2893C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341251 | ||||||
| chr9:70341371
|
A | G | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2398-2773A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341371 | ||||||
| chr9:70341542
|
A | G | 61 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(58): Show | 63 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.2398-2602A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341542 | ||||||
| chr9:70341598
|
C | A | 118 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(115): Show | 124 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2398-2546C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341598 | ||||||
| chr9:70341607
|
C | A | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2398-2537C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341607 | ||||||
| chr9:70341642
|
T | G | 56 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(53): Show | 60 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2398-2502T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341642 | ||||||
| chr9:70341781
|
A | G | 161 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(158): Show | 170 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2398-2363A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341781 | ||||||
| chr9:70341841
|
A | G | 116 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(113): Show | 122 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2398-2303A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341841 | ||||||
| chr9:70341944
|
A | G | 118 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(115): Show | 124 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2398-2200A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341944 | ||||||
| chr9:70341952
|
C | T | 153 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(150): Show | 162 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.2398-2192C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341952 | ||||||
| chr9:70341953
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-2191G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341953 | ||||||
| chr9:70342057
|
C | T | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2398-2087C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342057 | ||||||
| chr9:70342092
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-2052A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342092 | ||||||
| chr9:70342116
|
A | G | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2398-2028A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342116 | ||||||
| chr9:70342224
|
G | C | 279 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(276): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.2398-1920G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342224 | ||||||
| chr9:70342230
|
G | A | 3 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020 | 3 | HG02572.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2398-1914G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342230 | ||||||
| chr9:70342253
|
G | T | 1 | a0016c0022t0012g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2398-1891G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342253 | ||||||
| chr9:70342320
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-1824C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342320 | ||||||
| chr9:70342407
|
A | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-1737A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342407 | ||||||
| chr9:70342440
|
C | T | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2398-1704C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342440 | ||||||
| chr9:70342625
|
C | G | 60 | a0003c0003t0001g0003a0003c0003t0001g0010a0003c0003t0001g0106others(57): Show | 63 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2398-1519C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342625 | ||||||
| chr9:70342696
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2398-1448A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342696 | ||||||
| chr9:70342770
|
G | T | 3 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0288 | 3 | NA18961.hp1 NA18994.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2398-1374G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342770 | ||||||
| chr9:70342846
|
G | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2398-1298G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342846 | ||||||
| chr9:70342884
|
T | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-1260T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342884 | ||||||
| chr9:70342909
|
G | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-1235G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342909 | ||||||
| chr9:70343147
|
C | CT | 94 | a0001c0001t0021g0317a0002c0002t0001g0002a0002c0002t0001g0004others(91): Show | 98 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2398-983dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70343147 | |||||
| chr9:70343147
|
C | CTT | 27 | a0002c0002t0001g0006a0002c0002t0001g0059a0002c0002t0001g0071others(24): Show | 29 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.2398-984_2398-983d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70343147 | |||||
| chr9:70343149
|
T | C | 2 | a0001c0001t0002g0267a0001c0001t0002g0276 | 2 | HG00741.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2398-995T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343149 | ||||||
| chr9:70343262
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-882C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343262 | ||||||
| chr9:70343263
|
G | A | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2398-881G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343263 | ||||||
| chr9:70343321
|
T | A | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2398-823T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343321 | ||||||
| chr9:70343331
|
G | A | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2398-813G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343331 | ||||||
| chr9:70343680
|
G | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-464G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343680 | ||||||
| chr9:70343722
|
G | A | 158 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(155): Show | 167 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.2398-422G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343722 | ||||||
| chr9:70343777
|
C | A | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2398-367C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343777 | ||||||
| chr9:70343872
|
AGCTAGAC others(12): Show |
A | 1 | a0007c0012t0001g0107 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2398-269_2398-251d others(21): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70343872 | |||||
| chr9:70344361
|
A | G | 1 | a0004c0004t0018g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2523+92A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344361 | ||||||
| chr9:70344390
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2523+121T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344390 | ||||||
| chr9:70344407
|
AAT | A | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2523+154_2523+155d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr9 | 70344407 | |||||
| chr9:70344499
|
G | A | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2523+230G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344499 | ||||||
| chr9:70344512
|
C | A | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2523+243C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344512 | ||||||
| chr9:70344597
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2523+328T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344597 | ||||||
| chr9:70344627
|
T | C | 1 | a0001c0001t0002g0008 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2523+358T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344627 | ||||||
| chr9:70344774
|
G | A | 5 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210others(2): Show | 5 | HG01884.hp1 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523+505G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344774 | ||||||
| chr9:70344776
|
T | A | 1 | a0004c0004t0001g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2523+507T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344776 | ||||||
| chr9:70344818
|
A | G | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2523+549A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344818 | ||||||
| chr9:70344840
|
C | T | 1 | a0002c0002t0010g0055 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2523+571C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344840 | ||||||
| chr9:70345140
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2523+871T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345140 | ||||||
| chr9:70345171
|
TCTA | T | 110 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(107): Show | 118 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2523+906_2523+908d others(5): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr9 | 70345171 | |||||
| chr9:70345174
|
ACT | A | 3 | a0001c0001t0002g0239a0001c0001t0002g0259a0001c0001t0002g0260 | 3 | HG02129.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2523+906_2523+907d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345174 | ||||||
| chr9:70345178
|
A | T | 3 | a0001c0001t0002g0239a0001c0001t0002g0259a0001c0001t0002g0260 | 3 | HG02129.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2523+909A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345178 | ||||||
| chr9:70345565
|
A | G | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2524-1040A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345565 | ||||||
| chr9:70345875
|
T | C | 341 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(338): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.2524-730T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345875 | ||||||
| chr9:70346407
|
C | T | 1 | a0002c0002t0001g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2524-198C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346407 | ||||||
| chr9:70346412
|
C | T | 1 | a0001c0001t0002g0269 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2524-193C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346412 | ||||||
| chr9:70346429
|
G | A | 1 | a0015c0020t0006g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2524-176G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346429 | ||||||
| chr9:70346487
|
G | A | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG00733.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2524-118G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346487 | ||||||
| chr9:70346514
|
T | A | 1 | a0004c0006t0001g0340 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2524-91T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346514 | ||||||
| chr9:70346668
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2568+19T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 19/24 | chr9 | 70346668 | ||||||
| chr9:70346729
|
C | T | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2568+80C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 19/24 | chr9 | 70346729 | ||||||
| chr9:70346905
|
C | T | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2569-161C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 19/24 | chr9 | 70346905 | ||||||
| chr9:70346946
|
C | A | 1 | a0001c0001t0002g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2569-120C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 19/24 | chr9 | 70346946 | ||||||
| chr9:70347179
|
T | C | 7 | a0003c0003t0001g0158a0003c0003t0001g0159a0003c0003t0001g0161others(4): Show | 7 | HG02080.hp2 HG02129.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.2664+18T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 20/24 | chr9 | 70347179 | ||||||
| chr9:70347238
|
G | C | 1 | a0004c0004t0001g0334 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2664+77G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 20/24 | chr9 | 70347238 | ||||||
| chr9:70347277
|
C | T | 1 | a0001c0005t0003g0022 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2664+116C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 20/24 | chr9 | 70347277 | ||||||
| chr9:70347900
|
A | G | 1 | a0001c0001t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2770-19A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 21/24 | chr9 | 70347900 | ||||||
| chr9:70348125
|
T | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889+87T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348125 | ||||||
| chr9:70348252
|
T | A | 111 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2889+214T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348252 | ||||||
| chr9:70348305
|
G | A | 13 | a0001c0001t0002g0120a0001c0001t0002g0243a0001c0001t0002g0244others(10): Show | 13 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.2889+267G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348305 | ||||||
| chr9:70348429
|
C | T | 55 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(52): Show | 59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2889+391C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348429 | ||||||
| chr9:70348430
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889+392G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348430 | ||||||
| chr9:70348486
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2889+448G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348486 | ||||||
| chr9:70348535
|
A | C | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889+497A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348535 | ||||||
| chr9:70348553
|
C | T | 1 | a0004c0004t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2889+515C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348553 | ||||||
| chr9:70348626
|
G | A | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2889+588G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348626 | ||||||
| chr9:70348652
|
C | T | 32 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0072others(29): Show | 34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2889+614C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348652 | ||||||
| chr9:70348667
|
G | T | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2889+629G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348667 | ||||||
| chr9:70348698
|
A | G | 1 | a0001c0001t0002g0271 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2889+660A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348698 | ||||||
| chr9:70348723
|
A | G | 2 | a0007c0012t0001g0107a0007c0012t0001g0179 | 2 | HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2889+685A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348723 | ||||||
| chr9:70348780
|
A | G | 1 | a0005c0007t0002g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2889+742A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348780 | ||||||
| chr9:70349034
|
A | G | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2889+996A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349034 | ||||||
| chr9:70349048
|
TTTAA | T | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2889+1014_2889+101 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr9 | 70349048 | |||||
| chr9:70349127
|
C | T | 1 | a0001c0001t0002g0298 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2890-987C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349127 | ||||||
| chr9:70349128
|
G | A | 3 | a0003c0003t0001g0153a0003c0003t0001g0155a0003c0003t0001g0201 | 3 | HG01496.hp2 HG02300.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2890-986G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349128 | ||||||
| chr9:70349131
|
A | G | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2890-983A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349131 | ||||||
| chr9:70349177
|
C | T | 1 | a0008c0021t0001g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2890-937C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349177 | ||||||
| chr9:70349181
|
T | C | 1 | a0002c0002t0001g0029 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2890-933T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349181 | ||||||
| chr9:70349193
|
A | G | 1 | a0016c0022t0012g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2890-921A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349193 | ||||||
| chr9:70349221
|
C | T | 1 | a0010c0016t0002g0301 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2890-893C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349221 | ||||||
| chr9:70349227
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2890-887C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349227 | ||||||
| chr9:70349239
|
G | T | 1 | a0002c0002t0019g0045 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2890-875G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349239 | ||||||
| chr9:70349346
|
C | T | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2890-768C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349346 | ||||||
| chr9:70349407
|
A | G | 1 | a0002c0002t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2890-707A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349407 | ||||||
| chr9:70349414
|
CATAGAAG others(19): Show |
C | 1 | a0002c0002t0001g0026 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2890-698_2890-673d others(28): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr9 | 70349414 | |||||
| chr9:70349623
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2890-491G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349623 | ||||||
| chr9:70349672
|
A | G | 8 | a0001c0005t0003g0018a0001c0005t0003g0019a0001c0005t0003g0020others(5): Show | 8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2890-442A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349672 | ||||||
| chr9:70349826
|
C | G | 7 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0002g0240others(4): Show | 7 | HG01099.hp2 HG01261.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2890-288C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349826 | ||||||
| chr9:70349851
|
A | G | 25 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(22): Show | 25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2890-263A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349851 | ||||||
| chr9:70349972
|
A | G | 1 | a0015c0020t0006g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2890-142A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349972 | ||||||
| chr9:70350092
|
T | A | 1 | a0001c0010t0002g0263 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2890-22T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70350092 | ||||||
| chr9:70350341
|
G | C | 1 | a0001c0001t0002g0298 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3070-35G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 23/24 | chr9 | 70350341 | ||||||
| chr9:70350361
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3070-15G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 23/24 | chr9 | 70350361 | ||||||
| chr9:70350522
|
A | G | 341 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(338): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.3165+51A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70350522 | ||||||
| chr9:70350704
|
T | C | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.3165+233T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70350704 | ||||||
| chr9:70350723
|
T | C | 158 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(155): Show | 167 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.3165+252T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70350723 | ||||||
| chr9:70350797
|
T | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3165+326T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70350797 | ||||||
| chr9:70351054
|
A | G | 1 | a0016c0022t0012g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3165+583A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351054 | ||||||
| chr9:70351146
|
G | A | 2 | a0006c0011t0009g0310a0006c0011t0009g0311 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3165+675G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351146 | ||||||
| chr9:70351227
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3165+756G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351227 | ||||||
| chr9:70351353
|
C | CA | 8 | a0001c0001t0002g0125a0001c0001t0002g0210a0001c0001t0017g0218others(5): Show | 8 | HG00741.hp1 HG01256.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.3166-822dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr9 | 70351353 | |||||
| chr9:70351703
|
A | T | 1 | a0013c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3166-488A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351703 | ||||||
| chr9:70351803
|
C | T | 121 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(118): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.3166-388C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351803 | ||||||
| chr9:70351853
|
A | T | 1 | a0002c0002t0013g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3166-338A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351853 | ||||||
| chr9:70351869
|
A | G | 26 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(23): Show | 26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.3166-322A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351869 | ||||||
| chr9:70351882
|
C | T | 5 | a0002c0009t0006g0095a0002c0009t0006g0098a0002c0009t0014g0097others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3166-309C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351882 | ||||||
| chr9:70351941
|
A | G | 220 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0011others(217): Show | 232 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.3166-250A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351941 | ||||||
| chr9:70352017
|
G | T | 6 | a0004c0008t0005g0100a0004c0008t0005g0101a0004c0008t0005g0102others(3): Show | 6 | HG00738.hp2 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.3166-174G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70352017 | ||||||
| chr9:70352036
|
G | A | 1 | a0002c0002t0001g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3166-155G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70352036 | ||||||
| chr9:70352070
|
G | GA | 27 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0322others(24): Show | 27 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.3166-112dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr9 | 70352070 | |||||
| chr9:70352148
|
C | A | 1 | a0004c0004t0018g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3166-43C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70352148 |