Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55206 |
|---|---|
| ensemblid | ENSG00000139697.14 |
| hgncid | 22973 |
| symbol | SBNO1 |
| name | strawberry notch homolog 1 |
| refseq_nuc | NM_001167856.3 |
| refseq_prot | NP_001161328.1 |
| ensembl_nuc | ENST00000602398.3 |
| ensembl_prot | ENSP00000473665.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 123289109 |
| end | 123364847 |
| strand | - |
| ver | v1.2 |
| region | chr12:123289109-123364847 |
| region5000 | chr12:123284109-123369847 |
| regionname0 | SBNO1_chr12_123289109_123364847 |
| regionname5000 | SBNO1_chr12_123284109_123369847 |
| 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 | 1/0 | 1393 | 215 | 71 | 41 | 79 | 5 | 18 | 59 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002 | 0/1 | 1393 | 31 | 6 | 14 | 0 | 3 | 7 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0003 | 0/0 | 1393 | 9 | 0 | 1 | 4 | 0 | 4 | 4 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0004 | 0/0 | 1393 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0005 | 0/0 | 1393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0006 | 0/0 | 1393 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| 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 | 4182 | 88 | 2 | 28 | 42 | 4 | 12 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0002 | 0/0 | 4182 | 42 | 2 | 5 | 33 | 0 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0003 | 0/0 | 4182 | 35 | 34 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0004 | 0/1 | 4182 | 31 | 6 | 14 | 0 | 3 | 7 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0005 | 0/0 | 4182 | 24 | 22 | 2 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0006 | 1/0 | 4182 | 14 | 3 | 4 | 3 | 1 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0007 | 0/0 | 4182 | 9 | 0 | 1 | 4 | 0 | 4 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0008 | 0/0 | 4182 | 4 | 4 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0009 | 0/0 | 4182 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0010 | 0/0 | 4182 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0011 | 0/0 | 4182 | 2 | 0 | 0 | 0 | 0 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0012 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0013 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0014 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0015 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0016 | 0/0 | 4182 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| c0017 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| 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 | 0/0 | 6944 | 42 | 1 | 6 | 30 | 0 | 5 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0002 | 0/1 | 6946 | 20 | 1 | 10 | 0 | 1 | 7 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0003 | 0/0 | 6933 | 20 | 0 | 4 | 13 | 0 | 3 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0004 | 0/0 | 6945 | 12 | 0 | 8 | 1 | 3 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0005 | 0/0 | 6955 | 9 | 8 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0006 | 0/0 | 6938 | 8 | 7 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0007 | 0/0 | 6945 | 7 | 0 | 2 | 2 | 0 | 3 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0008 | 0/0 | 6945 | 6 | 0 | 0 | 2 | 0 | 4 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0009 | 0/0 | 6933 | 6 | 0 | 0 | 6 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0010 | 0/0 | 6945 | 5 | 0 | 2 | 1 | 1 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0011 | 0/0 | 6945 | 4 | 2 | 1 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0012 | 0/0 | 6938 | 4 | 4 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0013 | 0/0 | 6943 | 4 | 0 | 2 | 1 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0014 | 0/0 | 6943 | 4 | 4 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0015 | 0/0 | 6937 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0016 | 0/0 | 6939 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0017 | 0/0 | 6943 | 3 | 0 | 0 | 2 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0018 | 0/0 | 6946 | 3 | 0 | 1 | 1 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0019 | 0/0 | 6945 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0020 | 0/0 | 6946 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0021 | 0/0 | 6934 | 3 | 0 | 0 | 3 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0022 | 0/0 | 6937 | 3 | 0 | 0 | 3 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0023 | 0/0 | 6954 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0024 | 0/0 | 6938 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0025 | 0/0 | 6939 | 2 | 1 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0026 | 0/0 | 6939 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0027 | 0/0 | 6944 | 2 | 0 | 2 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0028 | 0/0 | 6943 | 2 | 0 | 2 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0029 | 0/0 | 6945 | 2 | 0 | 0 | 2 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0030 | 0/0 | 6943 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0031 | 0/0 | 6945 | 2 | 0 | 2 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0032 | 0/0 | 6946 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0033 | 0/0 | 6947 | 2 | 0 | 0 | 0 | 0 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0034 | 0/0 | 6938 | 2 | 1 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0035 | 0/0 | 6944 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0036 | 0/0 | 6945 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0037 | 0/0 | 6944 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0038 | 0/0 | 6944 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0039 | 0/0 | 6944 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0040 | 0/0 | 6945 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0041 | 0/0 | 6946 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0042 | 0/0 | 6944 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0043 | 0/0 | 6947 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0044 | 0/0 | 6948 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0045 | 0/0 | 6949 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0046 | 0/0 | 6936 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0047 | 0/0 | 6937 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0048 | 0/0 | 6940 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0049 | 0/0 | 6940 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0050 | 0/0 | 6941 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0051 | 0/0 | 6944 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0052 | 0/0 | 6945 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0053 | 0/0 | 6944 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0054 | 0/0 | 6944 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0055 | 0/0 | 6944 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0056 | 0/0 | 6944 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0057 | 0/0 | 6944 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0058 | 0/0 | 6942 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0059 | 0/0 | 6944 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0060 | 0/0 | 6945 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0061 | 0/0 | 6945 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0062 | 0/0 | 6944 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0063 | 0/0 | 6946 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0064 | 0/0 | 6946 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0065 | 0/0 | 6945 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0066 | 0/0 | 6944 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0067 | 0/0 | 6944 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0068 | 0/0 | 6945 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0069 | 0/0 | 6945 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0070 | 0/0 | 6946 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0071 | 0/0 | 6947 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0072 | 0/0 | 6944 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0073 | 0/0 | 6945 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0074 | 0/0 | 6945 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0075 | 0/0 | 6946 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0076 | 0/0 | 6946 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0077 | 0/0 | 6947 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0078 | 0/0 | 6946 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0079 | 0/0 | 6945 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0080 | 0/0 | 6946 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0081 | 0/0 | 6946 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0082 | 0/0 | 6947 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0083 | 0/0 | 6937 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0084 | 0/0 | 6944 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0085 | 0/0 | 6938 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0086 | 0/0 | 6934 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0087 | 1/0 | 6947 | 1 | 0 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0088 | 0/0 | 6938 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0089 | 0/0 | 6936 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0090 | 0/0 | 6934 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0091 | 0/0 | 6938 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0092 | 0/0 | 6933 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0093 | 0/0 | 6933 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0094 | 0/0 | 6934 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| t0095 | 0/0 | 6933 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| 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 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| 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 | 4182 | 88 | 2 | 28 | 42 | 4 | 12 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002 | 0/0 | 4182 | 42 | 2 | 5 | 33 | 0 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003 | 0/0 | 4182 | 35 | 34 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005 | 0/0 | 4182 | 24 | 22 | 2 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0006 | 1/0 | 4182 | 14 | 3 | 4 | 3 | 1 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0008 | 0/0 | 4182 | 4 | 4 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0010 | 0/0 | 4182 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0011 | 0/0 | 4182 | 2 | 0 | 0 | 0 | 0 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0012 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0013 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0014 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0015 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004 | 0/1 | 4182 | 31 | 6 | 14 | 0 | 3 | 7 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0003c0007 | 0/0 | 4182 | 9 | 0 | 1 | 4 | 0 | 4 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0004c0009 | 0/0 | 4182 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0005c0017 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0006c0016 | 0/0 | 4182 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11125 | 41 | 1 | 6 | 30 | 0 | 4 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0004 | 0/0 | 11126 | 12 | 0 | 8 | 1 | 3 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0007 | 0/0 | 11126 | 7 | 0 | 2 | 2 | 0 | 3 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0013 | 0/0 | 11124 | 4 | 0 | 2 | 1 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0017 | 0/0 | 11124 | 3 | 0 | 0 | 2 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0018 | 0/0 | 11127 | 3 | 0 | 1 | 1 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0027 | 0/0 | 11125 | 2 | 0 | 2 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0028 | 0/0 | 11124 | 2 | 0 | 2 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0029 | 0/0 | 11126 | 2 | 0 | 0 | 2 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0033 | 0/0 | 11128 | 2 | 0 | 0 | 0 | 0 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0052 | 0/0 | 11126 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0053 | 0/0 | 11125 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0054 | 0/0 | 11125 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0055 | 0/0 | 11125 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0056 | 0/0 | 11125 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0057 | 0/0 | 11125 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0058 | 0/0 | 11123 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0063 | 0/0 | 11127 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0083 | 0/0 | 11118 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0001t0084 | 0/0 | 11125 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0003 | 0/0 | 11114 | 18 | 0 | 4 | 13 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0009 | 0/0 | 11114 | 6 | 0 | 0 | 6 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0021 | 0/0 | 11115 | 3 | 0 | 0 | 3 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0022 | 0/0 | 11118 | 3 | 0 | 0 | 3 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0034 | 0/0 | 11119 | 2 | 1 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0085 | 0/0 | 11119 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0086 | 0/0 | 11115 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0088 | 0/0 | 11119 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0089 | 0/0 | 11117 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0090 | 0/0 | 11115 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0091 | 0/0 | 11119 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0092 | 0/0 | 11114 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0093 | 0/0 | 11114 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0094 | 0/0 | 11115 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0002t0095 | 0/0 | 11114 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0005 | 0/0 | 11136 | 9 | 8 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0014 | 0/0 | 11124 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0019 | 0/0 | 11126 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0023 | 0/0 | 11135 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0030 | 0/0 | 11124 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0043 | 0/0 | 11128 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0044 | 0/0 | 11129 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0045 | 0/0 | 11130 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0064 | 0/0 | 11127 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0065 | 0/0 | 11126 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0066 | 0/0 | 11125 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0067 | 0/0 | 11125 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0068 | 0/0 | 11126 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0069 | 0/0 | 11126 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0071 | 0/0 | 11128 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0072 | 0/0 | 11125 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0073 | 0/0 | 11126 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0074 | 0/0 | 11126 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0076 | 0/0 | 11127 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0077 | 0/0 | 11128 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0003t0078 | 0/0 | 11127 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0006 | 0/0 | 11119 | 6 | 5 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0012 | 0/0 | 11119 | 4 | 4 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0015 | 0/0 | 11118 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0016 | 0/0 | 11120 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0025 | 0/0 | 11120 | 2 | 1 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0026 | 0/0 | 11120 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0046 | 0/0 | 11117 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0047 | 0/0 | 11118 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0048 | 0/0 | 11121 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0005t0049 | 0/0 | 11121 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0006t0010 | 0/0 | 11126 | 5 | 0 | 2 | 1 | 1 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0006t0011 | 0/0 | 11126 | 4 | 2 | 1 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0006t0035 | 0/0 | 11125 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0006t0037 | 0/0 | 11125 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0006t0038 | 0/0 | 11125 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0006t0040 | 0/0 | 11126 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0006t0087 | 1/0 | 11128 | 1 | 0 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0008t0006 | 0/0 | 11119 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0008t0024 | 0/0 | 11119 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0010t0060 | 0/0 | 11126 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0010t0061 | 0/0 | 11126 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0011t0003 | 0/0 | 11114 | 2 | 0 | 0 | 0 | 0 | 2 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0012t0050 | 0/0 | 11122 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0013t0070 | 0/0 | 11127 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0014t0036 | 0/0 | 11126 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0001c0015t0051 | 0/0 | 11125 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004t0002 | 0/1 | 11127 | 20 | 1 | 10 | 0 | 1 | 7 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004t0020 | 0/0 | 11127 | 3 | 3 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004t0031 | 0/0 | 11126 | 2 | 0 | 2 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004t0032 | 0/0 | 11127 | 2 | 2 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004t0079 | 0/0 | 11126 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004t0080 | 0/0 | 11127 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004t0081 | 0/0 | 11127 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0002c0004t0082 | 0/0 | 11128 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0003c0007t0008 | 0/0 | 11126 | 6 | 0 | 0 | 2 | 0 | 4 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0003c0007t0039 | 0/0 | 11125 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0003c0007t0041 | 0/0 | 11127 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0003c0007t0042 | 0/0 | 11125 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0004c0009t0014 | 0/0 | 11124 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0004c0009t0062 | 0/0 | 11125 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0004c0009t0075 | 0/0 | 11127 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0005c0017t0059 | 0/0 | 11125 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| a0006c0016t0001 | 0/0 | 11125 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | copy fasta | chr12 | 123284109 | 123369847 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0013g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0013g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0013g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0017g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0017g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0017g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0018g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0018g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0018g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0027g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0027g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0028g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0028g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0029g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0029g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0033g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0033g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0052g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0053g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0054g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0055g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0056g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0057g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0058g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0063g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0083g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0001t0084g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0009g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0009g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0009g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0009g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0021g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0021g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0021g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0022g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0022g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0022g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0034g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0034g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0085g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0086g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0088g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0089g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0090g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0091g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0092g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0093g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0094g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0002t0095g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0014g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0014g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0019g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0019g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0019g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0023g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0023g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0030g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0030g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0043g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0044g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0045g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0064g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0065g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0066g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0067g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0068g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0069g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0071g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0072g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0073g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0074g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0076g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0077g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0003t0078g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0015g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0015g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0015g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0016g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0016g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0025g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0025g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0026g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0026g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0046g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0047g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0048g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0005t0049g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0010g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0010g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0010g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0010g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0011g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0011g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0035g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0037g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0038g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0040g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0006t0087g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0008t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0008t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0008t0024g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0008t0024g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0010t0060g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0010t0061g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0011t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0011t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0012t0050g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0013t0070g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0014t0036g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0001c0015t0051g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0020g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0020g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0020g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0031g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0031g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0032g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0032g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0079g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0080g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0081g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0002c0004t0082g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0008g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0008g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0008g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0039g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0041g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0003c0007t0042g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0004c0009t0014g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0004c0009t0062g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0004c0009t0075g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0005c0017t0059g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| a0006c0016t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0132 | EUR | GBR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00140 | hp2 | a0002 | c0004 | t0081 | g0042 | EUR | GBR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0142 | EUR | FIN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00280 | hp2 | a0001 | c0006 | t0010 | g0013 | EUR | FIN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00621 | hp1 | a0001 | c0002 | t0021 | g0250 | EAS | CHS | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00639 | hp2 | a0001 | c0001 | t0027 | g0093 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0213 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0237 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0225 | EAS | CHS | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00735 | hp2 | a0001 | c0001 | t0027 | g0165 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0215 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00738 | hp2 | a0002 | c0004 | t0002 | g0059 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00741 | hp1 | a0002 | c0004 | t0002 | g0044 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0238 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01070 | hp1 | a0002 | c0004 | t0031 | g0060 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0227 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01071 | hp1 | a0002 | c0004 | t0002 | g0061 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01074 | hp1 | a0001 | c0001 | t0057 | g0131 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01074 | hp2 | a0002 | c0004 | t0079 | g0045 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01081 | hp1 | a0002 | c0004 | t0002 | g0046 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01099 | hp1 | a0001 | c0003 | t0005 | g0030 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01106 | hp2 | a0002 | c0004 | t0002 | g0055 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01109 | hp1 | a0001 | c0005 | t0025 | g0201 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01109 | hp2 | a0002 | c0004 | t0080 | g0051 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01167 | hp1 | a0001 | c0001 | t0058 | g0196 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01167 | hp2 | a0002 | c0004 | t0002 | g0049 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01175 | hp2 | a0001 | c0006 | t0011 | g0003 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01243 | hp1 | a0001 | c0005 | t0006 | g0106 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01243 | hp2 | a0001 | c0002 | t0034 | g0217 | AMR | PUR | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01256 | hp1 | a0002 | c0004 | t0031 | g0052 | AMR | CLM | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01256 | hp2 | a0001 | c0001 | t0013 | g0172 | AMR | CLM | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | CLM | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01261 | hp2 | a0002 | c0004 | t0002 | g0047 | AMR | CLM | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01358 | hp1 | a0003 | c0007 | t0041 | g0019 | AMR | CLM | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | CLM | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01516 | hp1 | a0001 | c0001 | t0018 | g0211 | EUR | IBS | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01516 | hp2 | a0002 | c0004 | t0082 | g0041 | EUR | IBS | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01884 | hp1 | a0001 | c0005 | t0016 | g0097 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01884 | hp2 | a0001 | c0003 | t0077 | g0063 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01891 | hp1 | a0001 | c0001 | t0053 | g0177 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01891 | hp2 | a0001 | c0003 | t0014 | g0075 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01928 | hp1 | a0001 | c0001 | t0056 | g0157 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01928 | hp2 | a0001 | c0001 | t0028 | g0152 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01943 | hp1 | a0001 | c0015 | t0051 | g0128 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01943 | hp2 | a0001 | c0006 | t0035 | g0012 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01952 | hp1 | a0001 | c0001 | t0084 | g0150 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01952 | hp2 | a0001 | c0006 | t0010 | g0009 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0151 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01978 | hp2 | a0002 | c0004 | t0002 | g0081 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01993 | hp1 | a0001 | c0001 | t0013 | g0127 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG01993 | hp2 | a0002 | c0004 | t0002 | g0057 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02055 | hp1 | a0001 | c0008 | t0024 | g0112 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02055 | hp2 | a0001 | c0003 | t0071 | g0067 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02071 | hp1 | a0001 | c0001 | t0018 | g0194 | EAS | KHV | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02071 | hp2 | a0001 | c0002 | t0009 | g0243 | EAS | KHV | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0249 | EAS | KHV | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02132 | hp1 | a0001 | c0014 | t0036 | g0008 | EAS | KHV | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02145 | hp1 | a0001 | c0010 | t0060 | g0130 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02145 | hp2 | a0001 | c0005 | t0026 | g0108 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02148 | hp1 | a0001 | c0001 | t0018 | g0144 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02148 | hp2 | a0001 | c0006 | t0010 | g0014 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0224 | EAS | CDX | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02257 | hp1 | a0001 | c0003 | t0005 | g0032 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02257 | hp2 | a0001 | c0005 | t0012 | g0114 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0025 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02280 | hp1 | a0002 | c0004 | t0020 | g0091 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02280 | hp2 | a0004 | c0009 | t0075 | g0088 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02293 | hp1 | a0001 | c0001 | t0052 | g0176 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0228 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02300 | hp1 | a0001 | c0001 | t0028 | g0178 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02300 | hp2 | a0002 | c0004 | t0002 | g0062 | AMR | PEL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02451 | hp1 | a0001 | c0005 | t0015 | g0207 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02451 | hp2 | a0001 | c0003 | t0014 | g0076 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02523 | hp2 | a0001 | c0002 | t0021 | g0254 | EAS | KHV | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02572 | hp1 | a0001 | c0003 | t0005 | g0028 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02572 | hp2 | a0001 | c0003 | t0068 | g0084 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02602 | hp1 | a0003 | c0007 | t0008 | g0001 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02622 | hp1 | a0001 | c0003 | t0064 | g0086 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02622 | hp2 | a0001 | c0003 | t0005 | g0037 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02630 | hp1 | a0001 | c0003 | t0005 | g0026 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02630 | hp2 | a0001 | c0013 | t0070 | g0193 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02647 | hp1 | a0001 | c0005 | t0006 | g0104 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02647 | hp2 | a0001 | c0003 | t0023 | g0029 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02683 | hp1 | a0001 | c0006 | t0011 | g0004 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02683 | hp2 | a0001 | c0001 | t0017 | g0136 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02717 | hp1 | a0001 | c0005 | t0048 | g0118 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02717 | hp2 | a0001 | c0003 | t0005 | g0031 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02735 | hp1 | a0002 | c0004 | t0002 | g0092 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0236 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02738 | hp1 | a0001 | c0001 | t0063 | g0188 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02738 | hp2 | a0001 | c0002 | t0090 | g0222 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02809 | hp1 | a0001 | c0012 | t0050 | g0123 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02809 | hp2 | a0001 | c0003 | t0045 | g0027 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02818 | hp1 | a0001 | c0005 | t0015 | g0205 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02818 | hp2 | a0001 | c0003 | t0044 | g0034 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02886 | hp1 | a0001 | c0008 | t0024 | g0100 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02886 | hp2 | a0001 | c0003 | t0069 | g0089 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02895 | hp1 | a0001 | c0005 | t0006 | g0116 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02895 | hp2 | a0001 | c0003 | t0019 | g0080 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02896 | hp1 | a0002 | c0004 | t0020 | g0078 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02896 | hp2 | a0001 | c0005 | t0046 | g0102 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02897 | hp1 | a0001 | c0003 | t0019 | g0065 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02897 | hp2 | a0001 | c0005 | t0047 | g0103 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02922 | hp1 | a0004 | c0009 | t0062 | g0087 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02922 | hp2 | a0001 | c0010 | t0061 | g0119 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02965 | hp1 | a0001 | c0003 | t0066 | g0069 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02965 | hp2 | a0001 | c0003 | t0014 | g0074 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02970 | hp1 | a0001 | c0006 | t0040 | g0022 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02970 | hp2 | a0001 | c0005 | t0012 | g0111 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02976 | hp1 | a0001 | c0002 | t0085 | g0209 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02976 | hp2 | a0001 | c0003 | t0023 | g0024 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03017 | hp1 | a0002 | c0004 | t0002 | g0038 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03017 | hp2 | a0001 | c0001 | t0013 | g0148 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03041 | hp1 | a0004 | c0009 | t0014 | g0082 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03041 | hp2 | a0002 | c0004 | t0032 | g0073 | AFR | GWD | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03098 | hp1 | a0001 | c0003 | t0043 | g0035 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03098 | hp2 | a0001 | c0005 | t0026 | g0101 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03139 | hp1 | a0002 | c0004 | t0020 | g0039 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03139 | hp2 | a0001 | c0005 | t0012 | g0110 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03195 | hp1 | a0001 | c0003 | t0072 | g0068 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03195 | hp2 | a0001 | c0008 | t0006 | g0095 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03209 | hp1 | a0001 | c0005 | t0049 | g0107 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03209 | hp2 | a0001 | c0005 | t0016 | g0096 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03225 | hp1 | a0001 | c0003 | t0005 | g0033 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03225 | hp2 | a0001 | c0005 | t0016 | g0098 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03239 | hp2 | a0001 | c0006 | t0010 | g0011 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03486 | hp1 | a0001 | c0003 | t0030 | g0090 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03486 | hp2 | a0001 | c0003 | t0005 | g0036 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03490 | hp1 | a0002 | c0004 | t0002 | g0050 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03490 | hp2 | a0001 | c0001 | t0033 | g0167 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03491 | hp2 | a0003 | c0007 | t0008 | g0021 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03492 | hp1 | a0003 | c0007 | t0008 | g0020 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03492 | hp2 | a0001 | c0001 | t0033 | g0186 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03516 | hp1 | a0001 | c0002 | t0034 | g0218 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03516 | hp2 | a0001 | c0005 | t0015 | g0206 | AFR | ESN | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03654 | hp1 | a0002 | c0004 | t0002 | g0056 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03688 | hp1 | a0002 | c0004 | t0002 | g0048 | SAS | STU | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0179 | SAS | STU | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03831 | hp1 | a0001 | c0011 | t0003 | g0235 | SAS | BEB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0200 | SAS | BEB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03942 | hp1 | a0002 | c0004 | t0002 | g0054 | SAS | BEB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0147 | SAS | BEB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG04199 | hp1 | a0003 | c0007 | t0008 | g0016 | SAS | STU | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG04199 | hp2 | a0002 | c0004 | t0002 | g0043 | SAS | STU | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG04228 | hp1 | a0006 | c0016 | t0001 | g0191 | SAS | STU | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG04228 | hp2 | a0001 | c0011 | t0003 | g0234 | SAS | STU | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0257 | EAS | CHB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0248 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18942 | hp1 | a0001 | c0002 | t0089 | g0247 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0231 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18949 | hp2 | a0001 | c0002 | t0091 | g0223 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18951 | hp2 | a0003 | c0007 | t0039 | g0005 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18952 | hp2 | a0001 | c0002 | t0095 | g0260 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18953 | hp1 | a0001 | c0002 | t0022 | g0255 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18957 | hp2 | a0001 | c0001 | t0017 | g0185 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0259 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18972 | hp1 | a0001 | c0006 | t0037 | g0006 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18972 | hp2 | a0001 | c0002 | t0021 | g0244 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18977 | hp1 | a0003 | c0007 | t0042 | g0015 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18981 | hp1 | a0005 | c0017 | t0059 | g0184 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18981 | hp2 | a0001 | c0002 | t0094 | g0240 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18990 | hp1 | a0001 | c0001 | t0017 | g0129 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0219 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18991 | hp2 | a0001 | c0002 | t0009 | g0241 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18995 | hp2 | a0001 | c0002 | t0009 | g0251 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0232 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19000 | hp1 | a0001 | c0002 | t0093 | g0245 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19003 | hp1 | a0001 | c0001 | t0029 | g0137 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0258 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19005 | hp1 | a0003 | c0007 | t0008 | g0017 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19043 | hp1 | a0001 | c0003 | t0019 | g0064 | AFR | LWK | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19043 | hp2 | a0001 | c0003 | t0065 | g0072 | AFR | LWK | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19054 | hp1 | a0001 | c0002 | t0086 | g0220 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19054 | hp2 | a0001 | c0001 | t0029 | g0133 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19055 | hp2 | a0001 | c0002 | t0022 | g0230 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19056 | hp1 | a0001 | c0006 | t0038 | g0010 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19056 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19057 | hp2 | a0003 | c0007 | t0008 | g0018 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19063 | hp2 | a0001 | c0002 | t0092 | g0226 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19064 | hp1 | a0001 | c0002 | t0009 | g0252 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19064 | hp2 | a0001 | c0001 | t0083 | g0124 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19067 | hp1 | a0001 | c0001 | t0055 | g0189 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19067 | hp2 | a0001 | c0002 | t0009 | g0242 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19082 | hp1 | a0001 | c0002 | t0088 | g0239 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19082 | hp2 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19084 | hp1 | a0001 | c0002 | t0009 | g0253 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19084 | hp2 | a0001 | c0001 | t0013 | g0192 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19085 | hp1 | a0001 | c0001 | t0054 | g0164 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19085 | hp2 | a0001 | c0006 | t0010 | g0007 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19090 | hp1 | a0001 | c0002 | t0022 | g0256 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19240 | hp1 | a0001 | c0003 | t0074 | g0083 | AFR | YRI | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA19240 | hp2 | a0001 | c0003 | t0076 | g0071 | AFR | YRI | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA20129 | hp1 | a0001 | c0005 | t0006 | g0105 | AFR | ASW | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA20129 | hp2 | a0001 | c0006 | t0011 | g0002 | AFR | ASW | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0139 | EUR | TSI | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA20805 | hp2 | a0002 | c0004 | t0002 | g0040 | EUR | TSI | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02109 | hp1 | a0001 | c0005 | t0012 | g0117 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02109 | hp2 | a0002 | c0004 | t0032 | g0079 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02486 | hp1 | a0001 | c0005 | t0006 | g0109 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02486 | hp2 | a0001 | c0003 | t0073 | g0070 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02559 | hp1 | a0001 | c0003 | t0078 | g0077 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG02559 | hp2 | a0001 | c0003 | t0030 | g0085 | AFR | ACB | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03471 | hp1 | a0001 | c0005 | t0006 | g0115 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| HG03471 | hp2 | a0001 | c0006 | t0011 | g0023 | AFR | MSL | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA20300 | hp1 | a0001 | c0005 | t0025 | g0094 | AFR | USA | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA20300 | hp2 | a0002 | c0004 | t0002 | g0058 | AFR | USA | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA21309 | hp1 | a0001 | c0008 | t0006 | g0113 | AFR | LWK | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| NA21309 | hp2 | a0001 | c0003 | t0067 | g0066 | AFR | LWK | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0004 | t0002 | g0053 | REF | REF | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| homoSapiens_grch38 | hp1 | a0001 | c0006 | t0087 | g0221 | REF | REF | SBNO1_chr12_123284109_123369847 | SBNO1 | chr12 | 123284109 | 123369847 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123313662
|
T | C | 1 | a0003 | 9 | HG01358.hp1 HG02602.hp1 HG03491.hp2 others(6): Show |
missense_variant | MODERATE | c.3178A>G | p.Met1060Val | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/32 | 3325/11128 | 3178/4182 | 1060/1393 | chr12 | 123313662 | ||
| chr12:123321672
|
C | T | 1 | a0002 | 31 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
missense_variant | MODERATE | c.2186G>A | p.Ser729Asn | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 17/32 | 2333/11128 | 2186/4182 | 729/1393 | chr12 | 123321672 | ||
| chr12:123323693
|
T | C | 1 | a0006 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2112A>G | p.Ile704Met | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/32 | 2259/11128 | 2112/4182 | 704/1393 | chr12 | 123323693 | ||
| chr12:123341055
|
G | A | 1 | a0005 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.584C>T | p.Ser195Phe | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/32 | 731/11128 | 584/4182 | 195/1393 | chr12 | 123341055 | ||
| chr12:123341088
|
G | A | 1 | a0004 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
missense_variant&splice_region_variant | MODERATE | c.551C>T | p.Thr184Ile | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/32 | 698/11128 | 551/4182 | 184/1393 | chr12 | 123341088 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123309316
|
T | C | 1 | a0001c0008 | 4 | HG02055.hp1 HG02886.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.3624A>G | p.Ser1208Ser | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/32 | 3771/11128 | 3624/4182 | 1208/1393 | chr12 | 123309316 | ||
| chr12:123309379
|
T | C | 1 | a0001c0015 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.3561A>G | p.Ser1187Ser | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/32 | 3708/11128 | 3561/4182 | 1187/1393 | chr12 | 123309379 | ||
| chr12:123309557
|
G | T | 2 | a0001c0002a0001c0011 | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
synonymous_variant | LOW | c.3469C>A | p.Arg1157Arg | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 27/32 | 3616/11128 | 3469/4182 | 1157/1393 | chr12 | 123309557 | ||
| chr12:123315382
|
A | G | 1 | a0001c0014 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.3111T>C | p.Phe1037Phe | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/32 | 3258/11128 | 3111/4182 | 1037/1393 | chr12 | 123315382 | ||
| chr12:123315391
|
C | T | 2 | a0001c0002a0001c0011 | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
synonymous_variant | LOW | c.3102G>A | p.Arg1034Arg | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/32 | 3249/11128 | 3102/4182 | 1034/1393 | chr12 | 123315391 | ||
| chr12:123315427
|
A | G | 11 | a0001c0001a0001c0002a0001c0005others(8): Show | 167 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(164): Show |
synonymous_variant | LOW | c.3066T>C | p.Gly1022Gly | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/32 | 3213/11128 | 3066/4182 | 1022/1393 | chr12 | 123315427 | ||
| chr12:123317309
|
T | C | 3 | a0001c0005a0001c0008a0001c0012 | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
synonymous_variant | LOW | c.2847A>G | p.Gln949Gln | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/32 | 2994/11128 | 2847/4182 | 949/1393 | chr12 | 123317309 | ||
| chr12:123326326
|
G | A | 4 | a0001c0001a0001c0015a0005c0017others(1): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
synonymous_variant | LOW | c.1701C>T | p.Ile567Ile | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 14/32 | 1848/11128 | 1701/4182 | 567/1393 | chr12 | 123326326 | ||
| chr12:123327748
|
T | C | 1 | a0001c0011 | 2 | HG03831.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.1497A>G | p.Pro499Pro | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 12/32 | 1644/11128 | 1497/4182 | 499/1393 | chr12 | 123327748 | ||
| chr12:123328764
|
C | G | 1 | a0001c0013 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1266G>C | p.Leu422Leu | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/32 | 1413/11128 | 1266/4182 | 422/1393 | chr12 | 123328764 | ||
| chr12:123341012
|
C | T | 3 | a0001c0003a0002c0004a0004c0009 | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
synonymous_variant | LOW | c.627G>A | p.Lys209Lys | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/32 | 774/11128 | 627/4182 | 209/1393 | chr12 | 123341012 | ||
| chr12:123345412
|
C | T | 1 | a0001c0012 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.396G>A | p.Pro132Pro | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/32 | 543/11128 | 396/4182 | 132/1393 | chr12 | 123345412 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123289174
|
G | GA | 14 | a0001c0002t0092a0001c0005t0006a0001c0005t0012others(11): Show | 30 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6733dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6733 | chr12 | 123289174 | |||||
| chr12:123289435
|
G | A | 4 | a0001c0003t0019a0001c0003t0067a0001c0003t0076others(1): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6473C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6473 | chr12 | 123289435 | |||||
| chr12:123289495
|
C | T | 3 | a0001c0002t0009a0001c0002t0021a0001c0002t0088 | 10 | HG00621.hp1 HG02071.hp2 HG02523.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6413G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6413 | chr12 | 123289495 | |||||
| chr12:123289562
|
T | C | 1 | a0001c0001t0054 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6346A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6346 | chr12 | 123289562 | |||||
| chr12:123289581
|
C | T | 1 | a0002c0004t0020 | 3 | HG02280.hp1 HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6327G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6327 | chr12 | 123289581 | |||||
| chr12:123289586
|
A | G | 1 | a0001c0001t0029 | 2 | NA19003.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6322T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6322 | chr12 | 123289586 | |||||
| chr12:123289595
|
T | C | 1 | a0001c0003t0065 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6313A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6313 | chr12 | 123289595 | |||||
| chr12:123289606
|
C | T | 1 | a0001c0014t0036 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6302G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6302 | chr12 | 123289606 | |||||
| chr12:123289759
|
T | C | 1 | a0001c0010t0061 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6149A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 6149 | chr12 | 123289759 | |||||
| chr12:123290113
|
C | T | 1 | a0001c0006t0040 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5795G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5795 | chr12 | 123290113 | |||||
| chr12:123290323
|
C | G | 4 | a0001c0003t0030a0001c0003t0064a0001c0003t0068others(1): Show | 5 | HG02559.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5585G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5585 | chr12 | 123290323 | |||||
| chr12:123290350
|
G | A | 1 | a0001c0001t0055 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5558C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5558 | chr12 | 123290350 | |||||
| chr12:123290393
|
G | C | 4 | a0003c0007t0008a0003c0007t0039a0003c0007t0041others(1): Show | 9 | HG01358.hp1 HG02602.hp1 HG03491.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5515C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5515 | chr12 | 123290393 | |||||
| chr12:123290412
|
T | C | 1 | a0002c0004t0080 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5496A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5496 | chr12 | 123290412 | |||||
| chr12:123290534
|
G | A | 1 | a0002c0004t0081 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5374C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5374 | chr12 | 123290534 | |||||
| chr12:123290580
|
G | A | 27 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(24): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5328C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5328 | chr12 | 123290580 | |||||
| chr12:123290604
|
G | A | 1 | a0001c0001t0056 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5304C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5304 | chr12 | 123290604 | |||||
| chr12:123290717
|
T | C | 16 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(13): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5191A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5191 | chr12 | 123290717 | |||||
| chr12:123290742
|
C | CT | 11 | a0001c0006t0010a0001c0006t0011a0001c0006t0035others(8): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5165dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5165 | chr12 | 123290742 | |||||
| chr12:123290769
|
G | C | 3 | a0001c0010t0060a0001c0010t0061a0001c0013t0070 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5139C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5139 | chr12 | 123290769 | |||||
| chr12:123290838
|
T | C | 27 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(24): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5070A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5070 | chr12 | 123290838 | |||||
| chr12:123290886
|
C | T | 1 | a0001c0005t0012 | 4 | HG02109.hp1 HG02257.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5022G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5022 | chr12 | 123290886 | |||||
| chr12:123290905
|
G | GT | 11 | a0001c0001t0083a0001c0003t0071a0001c0006t0010others(8): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5002dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5002 | chr12 | 123290905 | |||||
| chr12:123290905
|
GT | G | 14 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(11): Show | 42 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*5002delA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 5002 | chr12 | 123290905 | |||||
| chr12:123290994
|
C | T | 1 | a0001c0008t0024 | 2 | HG02055.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4914G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4914 | chr12 | 123290994 | |||||
| chr12:123291217
|
A | G | 4 | a0001c0002t0009a0001c0002t0021a0001c0002t0088others(1): Show | 11 | HG00621.hp1 HG02071.hp2 HG02523.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4691T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4691 | chr12 | 123291217 | |||||
| chr12:123291255
|
T | C | 13 | a0001c0005t0006a0001c0005t0012a0001c0005t0015others(10): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4653A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4653 | chr12 | 123291255 | |||||
| chr12:123291604
|
A | C | 16 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(13): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*4304T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4304 | chr12 | 123291604 | |||||
| chr12:123291612
|
T | C | 1 | a0001c0001t0057 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4296A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4296 | chr12 | 123291612 | |||||
| chr12:123291679
|
T | TA | 5 | a0001c0001t0004a0001c0001t0018a0001c0003t0044others(2): Show | 18 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4228dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4228 | chr12 | 123291679 | |||||
| chr12:123291679
|
TA | T | 33 | a0001c0001t0013a0001c0001t0058a0001c0003t0014others(30): Show | 86 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*4228delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4228 | chr12 | 123291679 | |||||
| chr12:123291679
|
TAA | T | 6 | a0001c0003t0030a0001c0005t0046a0001c0006t0011others(3): Show | 10 | HG01074.hp2 HG01175.hp2 HG01943.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4227_*4228delTT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4227 | chr12 | 123291679 | |||||
| chr12:123291679
|
TAAAA | T | 11 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(8): Show | 38 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4225_*4228delTTTT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4225 | chr12 | 123291679 | |||||
| chr12:123291703
|
A | C | 1 | a0001c0005t0026 | 2 | HG02145.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4205T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4205 | chr12 | 123291703 | |||||
| chr12:123291703
|
A | T | 1 | a0001c0001t0053 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4205T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4205 | chr12 | 123291703 | |||||
| chr12:123291735
|
G | T | 1 | a0001c0003t0064 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4173C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 4173 | chr12 | 123291735 | |||||
| chr12:123291919
|
C | CA | 15 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(12): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3988dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3988 | chr12 | 123291919 | |||||
| chr12:123292021
|
A | AT | 58 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(55): Show | 179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*3886dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3886 | chr12 | 123292021 | |||||
| chr12:123292021
|
A | ATT | 5 | a0001c0001t0052a0001c0001t0063a0001c0002t0085others(2): Show | 5 | HG02293.hp1 HG02738.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3885_*3886dupAA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3886 | chr12 | 123292021 | |||||
| chr12:123292021
|
A | T | 1 | a0001c0002t0089 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3887T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3887 | chr12 | 123292021 | |||||
| chr12:123292068
|
T | G | 1 | a0001c0006t0040 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3840A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3840 | chr12 | 123292068 | |||||
| chr12:123292103
|
C | T | 1 | a0001c0001t0027 | 2 | HG00639.hp2 HG00735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3805G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3805 | chr12 | 123292103 | |||||
| chr12:123292115
|
G | T | 1 | a0001c0015t0051 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3793C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3793 | chr12 | 123292115 | |||||
| chr12:123292202
|
T | C | 4 | a0003c0007t0008a0003c0007t0039a0003c0007t0041others(1): Show | 9 | HG01358.hp1 HG02602.hp1 HG03491.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3706A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3706 | chr12 | 123292202 | |||||
| chr12:123292426
|
T | C | 1 | a0005c0017t0059 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3482A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3482 | chr12 | 123292426 | |||||
| chr12:123292719
|
T | C | 1 | a0001c0013t0070 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3189A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3189 | chr12 | 123292719 | |||||
| chr12:123292771
|
G | A | 1 | a0001c0002t0034 | 2 | HG01243.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3137C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 3137 | chr12 | 123292771 | |||||
| chr12:123293164
|
T | C | 1 | a0002c0004t0032 | 2 | HG02109.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2744A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 2744 | chr12 | 123293164 | |||||
| chr12:123293268
|
G | T | 27 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(24): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2640C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 2640 | chr12 | 123293268 | |||||
| chr12:123293284
|
G | A | 5 | a0001c0006t0010a0001c0006t0035a0001c0006t0037others(2): Show | 9 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2624C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 2624 | chr12 | 123293284 | |||||
| chr12:123293320
|
T | G | 1 | a0001c0002t0085 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2588A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 2588 | chr12 | 123293320 | |||||
| chr12:123293528
|
G | A | 1 | a0001c0012t0050 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2380C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 2380 | chr12 | 123293528 | |||||
| chr12:123293632
|
T | C | 1 | a0001c0003t0077 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2276A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 2276 | chr12 | 123293632 | |||||
| chr12:123293808
|
G | C | 4 | a0001c0003t0071a0001c0003t0072a0001c0003t0073others(1): Show | 4 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2100C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 2100 | chr12 | 123293808 | |||||
| chr12:123293908
|
TCCA | T | 27 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(24): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1997_*1999delTGG | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1997 | chr12 | 123293908 | |||||
| chr12:123293922
|
G | T | 5 | a0001c0006t0010a0001c0006t0035a0001c0006t0037others(2): Show | 9 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1986C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1986 | chr12 | 123293922 | |||||
| chr12:123294207
|
A | ACGGTAAG | 11 | a0001c0006t0010a0001c0006t0011a0001c0006t0035others(8): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1694_*1700dupCTTA others(3): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1700 | chr12 | 123294207 | |||||
| chr12:123294257
|
GA | G | 23 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(20): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1650delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1650 | chr12 | 123294257 | |||||
| chr12:123294634
|
CA | C | 13 | a0001c0003t0074a0001c0003t0076a0001c0003t0077others(10): Show | 27 | HG01070.hp1 HG01109.hp1 HG01243.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1273delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1273 | chr12 | 123294634 | |||||
| chr12:123294634
|
CAA | C | 18 | a0001c0001t0007a0001c0001t0018a0001c0001t0029others(15): Show | 30 | HG00738.hp1 HG01516.hp1 HG01978.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1272_*1273delTT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1272 | chr12 | 123294634 | |||||
| chr12:123294634
|
CAAA | C | 26 | a0001c0001t0001a0001c0001t0004a0001c0001t0013others(23): Show | 87 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1271_*1273delTTT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1271 | chr12 | 123294634 | |||||
| chr12:123294634
|
CAAAA | C | 11 | a0001c0001t0017a0001c0002t0003a0001c0002t0009others(8): Show | 36 | HG00642.hp2 HG00673.hp1 HG01069.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1270_*1273delTTTT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1270 | chr12 | 123294634 | |||||
| chr12:123294651
|
AAAAAAAA others(4): Show |
A | 9 | a0001c0001t0083a0001c0006t0010a0001c0006t0035others(6): Show | 18 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1246_*1256delCTTT others(7): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1246 | chr12 | 123294651 | |||||
| chr12:123294652
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0006t0011a0001c0006t0040a0003c0007t0041 | 6 | HG01175.hp2 HG01358.hp1 HG02683.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1246_*1255delCTTT others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1246 | chr12 | 123294652 | |||||
| chr12:123294654
|
A | AAAAAAG | 2 | a0001c0003t0005a0001c0003t0023 | 11 | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1253_*1254insCTTT others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1253 | chr12 | 123294654 | |||||
| chr12:123294666
|
A | AG | 3 | a0001c0003t0005a0001c0003t0023a0001c0003t0045 | 12 | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1241_*1242insC | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1241 | chr12 | 123294666 | |||||
| chr12:123294670
|
G | GA | 3 | a0001c0003t0005a0001c0003t0023a0001c0003t0045 | 12 | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1237dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1237 | chr12 | 123294670 | |||||
| chr12:123294671
|
AAAAG | A | 16 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(13): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1233_*1236delCTTT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1233 | chr12 | 123294671 | |||||
| chr12:123294868
|
GTAACAAC others(2): Show |
G | 13 | a0001c0005t0006a0001c0005t0012a0001c0005t0015others(10): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1039delTTGT others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 1031 | chr12 | 123294868 | |||||
| chr12:123294942
|
G | A | 27 | a0001c0002t0003a0001c0002t0009a0001c0002t0021others(24): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*966C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 966 | chr12 | 123294942 | |||||
| chr12:123294982
|
T | A | 1 | a0003c0007t0042 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*926A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 926 | chr12 | 123294982 | |||||
| chr12:123295061
|
T | A | 1 | a0001c0002t0034 | 2 | HG01243.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*847A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 847 | chr12 | 123295061 | |||||
| chr12:123295345
|
T | G | 1 | a0001c0001t0084 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*563A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 563 | chr12 | 123295345 | |||||
| chr12:123295402
|
T | C | 1 | a0001c0001t0033 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*506A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 506 | chr12 | 123295402 | |||||
| chr12:123295593
|
G | A | 1 | a0001c0002t0095 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 315 | chr12 | 123295593 | |||||
| chr12:123295593
|
G | C | 1 | a0001c0002t0085 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*315C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 315 | chr12 | 123295593 | |||||
| chr12:123295714
|
A | G | 1 | a0001c0002t0086 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*194T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 32/32 | 194 | chr12 | 123295714 | |||||
| chr12:123364725
|
C | G | 83 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(80): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
5_prime_UTR_variant | MODIFIER | c.-25G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/32 | 14284 | chr12 | 123364725 | |||||
| chr12:123364797
|
A | G | 5 | a0001c0003t0005a0001c0003t0023a0001c0003t0043others(2): Show | 14 | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-97T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/32 | 14356 | chr12 | 123364797 | |||||
| chr12:123364800
|
A | AGCG | 11 | a0001c0006t0010a0001c0006t0011a0001c0006t0035others(8): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-103_-101dupCGC | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/32 | 14360 | chr12 | 123364800 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123296153
|
CAAG | C | 2 | a0001c0001t0004g0132a0001c0001t0004g0143 | 2 | HG00140.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.4040-106_4040-104d others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296153 | ||||||
| chr12:123296332
|
G | A | 1 | a0001c0006t0011g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4040-282C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296332 | ||||||
| chr12:123296365
|
T | TTTTAAGC others(34): Show |
67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.4040-316_4040-315i others(43): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296365 | ||||||
| chr12:123296553
|
G | C | 5 | a0001c0003t0030g0085a0001c0003t0030g0090a0001c0003t0064g0086others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4040-503C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296553 | ||||||
| chr12:123296554
|
T | TG | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.4040-505dupC | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296554 | ||||||
| chr12:123296555
|
G | GT | 88 | a0001c0001t0001g0099a0001c0001t0001g0122a0001c0001t0001g0125others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.4040-506dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296555 | ||||||
| chr12:123296556
|
T | G | 3 | a0001c0010t0060g0130a0001c0010t0061g0119a0001c0013t0070g0193 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4040-506A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296556 | ||||||
| chr12:123296566
|
T | G | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.4040-516A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296566 | ||||||
| chr12:123296567
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4040-517C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296567 | ||||||
| chr12:123296586
|
G | T | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4040-536C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296586 | ||||||
| chr12:123296600
|
C | T | 1 | a0002c0004t0020g0078 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4040-550G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296600 | ||||||
| chr12:123296659
|
G | C | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.4040-609C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296659 | ||||||
| chr12:123296736
|
T | G | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.4040-686A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296736 | ||||||
| chr12:123296760
|
G | A | 3 | a0001c0003t0005g0028a0001c0003t0005g0030a0001c0003t0005g0031 | 3 | HG01099.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4040-710C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296760 | ||||||
| chr12:123296839
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.4040-789C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296839 | ||||||
| chr12:123296865
|
G | GT | 45 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(42): Show | 45 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.4040-816dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123296865 | ||||||
| chr12:123297135
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4039+843C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297135 | ||||||
| chr12:123297328
|
TCAAAAAA others(64): Show |
T | 5 | a0001c0002t0003g0246a0001c0002t0090g0222a0001c0002t0091g0223others(2): Show | 5 | HG02738.hp2 NA18949.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.4039+579_4039+649d others(73): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297328 | ||||||
| chr12:123297329
|
C | CA | 49 | a0001c0001t0001g0099a0001c0001t0001g0122a0001c0001t0001g0125others(46): Show | 49 | HG00438.hp2 HG00673.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.4039+648dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297329 | ||||||
| chr12:123297329
|
C | CAA | 33 | a0001c0001t0001g0120a0001c0001t0001g0146a0001c0001t0001g0153others(30): Show | 33 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.4039+647_4039+648d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297329 | ||||||
| chr12:123297329
|
C | CAAA | 10 | a0001c0001t0001g0126a0001c0001t0001g0149a0001c0001t0001g0161others(7): Show | 10 | HG00621.hp2 HG01175.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.4039+646_4039+648d others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297329 | ||||||
| chr12:123297329
|
CA | C | 17 | a0001c0005t0025g0201a0001c0005t0048g0118a0001c0006t0010g0007others(14): Show | 17 | HG01109.hp1 HG01358.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.4039+648delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297329 | ||||||
| chr12:123297329
|
CAA | C | 35 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(32): Show | 35 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.4039+647_4039+648d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297329 | ||||||
| chr12:123297329
|
CAAAAAAA others(65): Show |
C | 36 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(33): Show | 36 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.4039+577_4039+648d others(74): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297329 | ||||||
| chr12:123297329
|
CAAAAAAA others(66): Show |
C | 3 | a0001c0002t0003g0238a0001c0002t0003g0258a0001c0002t0085g0209 | 3 | HG01069.hp1 HG02976.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.4039+576_4039+648d others(75): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297329 | ||||||
| chr12:123297400
|
C | CA | 13 | a0001c0003t0019g0064a0001c0003t0019g0080a0001c0003t0066g0069others(10): Show | 13 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.4039+577dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAA | 5 | a0001c0001t0004g0132a0001c0001t0013g0148a0001c0006t0011g0004others(2): Show | 5 | HG00140.hp1 HG02683.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.4039+573_4039+577d others(7): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAA | 10 | a0001c0001t0083g0124a0001c0006t0011g0002a0001c0006t0011g0023others(7): Show | 10 | HG01358.hp1 HG02602.hp1 HG03471.hp2 others(7): Show |
intron_variant | MODIFIER | c.4039+572_4039+577d others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(3): Show |
7 | a0001c0005t0006g0105a0001c0006t0010g0007a0001c0006t0010g0009others(4): Show | 7 | HG01952.hp2 HG02132.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.4039+568_4039+577d others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(4): Show |
3 | a0001c0005t0046g0102a0001c0006t0037g0006a0001c0008t0006g0113 | 3 | HG02896.hp2 NA18972.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4039+567_4039+577d others(13): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(5): Show |
1 | a0001c0005t0047g0103 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4039+566_4039+577d others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(7): Show |
1 | a0001c0005t0006g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4039+564_4039+577d others(16): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0029g0133a0001c0001t0058g0196a0001c0005t0006g0115 | 3 | HG01167.hp1 HG03471.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.4039+563_4039+577d others(17): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(9): Show |
8 | a0001c0001t0001g0174a0001c0001t0001g0198a0001c0001t0001g0202others(5): Show | 8 | HG01175.hp1 HG01256.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.4039+562_4039+577d others(18): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(10): Show |
19 | a0001c0001t0001g0099a0001c0001t0001g0126a0001c0001t0001g0145others(16): Show | 19 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.4039+561_4039+577d others(19): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(11): Show |
24 | a0001c0001t0001g0135a0001c0001t0001g0146a0001c0001t0001g0158others(21): Show | 24 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.4039+560_4039+577d others(20): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(12): Show |
24 | a0001c0001t0001g0120a0001c0001t0001g0153a0001c0001t0001g0156others(21): Show | 24 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.4039+559_4039+577d others(21): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(13): Show |
5 | a0001c0001t0001g0181a0001c0001t0053g0177a0001c0005t0012g0110others(2): Show | 5 | HG00621.hp2 HG01891.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.4039+558_4039+577d others(22): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(14): Show |
3 | a0001c0005t0012g0111a0001c0005t0012g0114a0001c0005t0016g0097 | 3 | HG01884.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4039+557_4039+577d others(23): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(15): Show |
6 | a0001c0001t0004g0139a0001c0001t0018g0211a0001c0005t0006g0116others(3): Show | 6 | HG01516.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.4039+556_4039+577d others(24): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0163 | 2 | HG03654.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.4039+577_4039+578i others(25): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0155 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4039+577_4039+578i others(26): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(18): Show |
3 | a0001c0001t0004g0141a0001c0001t0004g0142a0001c0008t0006g0095 | 3 | HG00280.hp1 HG01981.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4039+577_4039+578i others(27): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(20): Show |
1 | a0001c0008t0024g0112 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4039+577_4039+578i others(29): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(22): Show |
1 | a0001c0010t0060g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4039+577_4039+578i others(31): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(25): Show |
1 | a0001c0008t0024g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4039+577_4039+578i others(34): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4039+577_4039+578i others(36): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
C | CAAAAAAA others(31): Show |
1 | a0001c0005t0049g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4039+577_4039+578i others(40): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297400
|
CA | C | 6 | a0001c0001t0001g0190a0001c0003t0023g0024a0001c0003t0030g0085others(3): Show | 6 | HG01167.hp2 HG01256.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.4039+577delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297400 | ||||||
| chr12:123297422
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0055g0189 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4039+555_4039+556i others(22): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297422 | ||||||
| chr12:123297492
|
G | A | 75 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(72): Show | 75 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.4039+486C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297492 | ||||||
| chr12:123297709
|
G | A | 1 | a0001c0003t0065g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4039+269C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297709 | ||||||
| chr12:123297779
|
T | A | 9 | a0001c0005t0016g0096a0001c0005t0016g0097a0001c0005t0016g0098others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4039+199A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297779 | ||||||
| chr12:123297810
|
G | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0199others(1): Show | 4 | HG02132.hp2 NA18953.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.4039+168C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297810 | ||||||
| chr12:123297898
|
A | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.4039+80T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 31/31 | chr12 | 123297898 | ||||||
| chr12:123298256
|
ATTTCT | A | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.3846-90_3846-86del others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298256 | ||||||
| chr12:123298270
|
C | T | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3846-99G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298270 | ||||||
| chr12:123298281
|
G | A | 4 | a0001c0005t0012g0110a0001c0005t0012g0111a0001c0005t0012g0114others(1): Show | 4 | HG02109.hp1 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3846-110C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298281 | ||||||
| chr12:123298302
|
T | G | 4 | a0001c0001t0001g0198a0001c0001t0013g0172a0001c0001t0013g0192others(1): Show | 4 | HG01256.hp2 HG02300.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.3846-131A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298302 | ||||||
| chr12:123298319
|
C | T | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.3846-148G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298319 | ||||||
| chr12:123298410
|
T | G | 45 | a0001c0001t0004g0143a0001c0002t0003g0219a0001c0002t0003g0224others(42): Show | 45 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.3846-239A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298410 | ||||||
| chr12:123298447
|
G | A | 1 | a0001c0005t0025g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3846-276C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298447 | ||||||
| chr12:123298534
|
C | T | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3846-363G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298534 | ||||||
| chr12:123298567
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0199others(1): Show | 4 | HG02132.hp2 NA18953.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.3846-396A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298567 | ||||||
| chr12:123298850
|
G | C | 1 | a0001c0010t0061g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3846-679C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298850 | ||||||
| chr12:123298933
|
T | G | 4 | a0001c0003t0030g0085a0001c0003t0030g0090a0001c0003t0064g0086others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3846-762A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298933 | ||||||
| chr12:123298936
|
A | G | 2 | a0001c0005t0006g0104a0001c0005t0006g0106 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3846-765T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123298936 | ||||||
| chr12:123299080
|
A | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3846-909T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299080 | ||||||
| chr12:123299144
|
T | A | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.3846-973A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299144 | ||||||
| chr12:123299185
|
G | A | 1 | a0001c0005t0006g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3846-1014C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299185 | ||||||
| chr12:123299375
|
A | C | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3846-1204T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299375 | ||||||
| chr12:123299389
|
A | G | 7 | a0001c0002t0009g0243a0001c0002t0009g0251a0001c0002t0009g0252others(4): Show | 7 | HG00621.hp1 HG02071.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.3846-1218T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299389 | ||||||
| chr12:123299409
|
C | T | 9 | a0003c0007t0008g0001a0003c0007t0008g0016a0003c0007t0008g0017others(6): Show | 9 | HG01358.hp1 HG02602.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.3846-1238G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299409 | ||||||
| chr12:123299447
|
C | T | 31 | a0002c0004t0002g0038a0002c0004t0002g0040a0002c0004t0002g0043others(28): Show | 31 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.3846-1276G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299447 | ||||||
| chr12:123299533
|
T | C | 3 | a0001c0003t0014g0074a0001c0003t0014g0075a0001c0003t0014g0076 | 3 | HG01891.hp2 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3846-1362A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299533 | ||||||
| chr12:123299543
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3846-1372A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299543 | ||||||
| chr12:123299681
|
C | CA | 11 | a0001c0003t0019g0064a0001c0003t0065g0072a0001c0003t0076g0071others(8): Show | 11 | HG00741.hp1 HG01167.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.3846-1511dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAA | 14 | a0001c0006t0010g0007a0001c0006t0010g0011a0001c0006t0010g0013others(11): Show | 14 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.3846-1512_3846-151 others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAA | 79 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(76): Show | 79 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.3846-1514_3846-151 others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAAA | 11 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0171others(8): Show | 11 | HG00642.hp1 HG00673.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3846-1515_3846-151 others(9): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0003g0225 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3846-1520_3846-151 others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAAAAA others(4): Show |
6 | a0001c0002t0003g0224a0001c0002t0003g0229a0001c0002t0003g0249others(3): Show | 6 | HG02080.hp1 HG02155.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.3846-1521_3846-151 others(15): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAAAAA others(5): Show |
18 | a0001c0002t0003g0219a0001c0002t0003g0227a0001c0002t0003g0231others(15): Show | 18 | HG01069.hp1 HG01070.hp2 HG02735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3846-1522_3846-151 others(16): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAAAAA others(6): Show |
8 | a0001c0002t0003g0237a0001c0002t0009g0243a0001c0002t0009g0252others(5): Show | 8 | HG00642.hp2 HG02071.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3846-1523_3846-151 others(17): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAAAAA others(7): Show |
5 | a0001c0002t0003g0228a0001c0002t0021g0244a0001c0002t0021g0250others(2): Show | 5 | HG00621.hp1 HG02293.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.3846-1524_3846-151 others(18): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAAAAA others(9): Show |
1 | a0001c0002t0091g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3846-1526_3846-151 others(20): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299681
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0092g0226 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3846-1511_3846-151 others(24): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299681 | ||||||
| chr12:123299691
|
A | C | 1 | a0001c0003t0074g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3846-1520T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299691 | ||||||
| chr12:123299695
|
A | AC | 9 | a0003c0007t0008g0001a0003c0007t0008g0016a0003c0007t0008g0017others(6): Show | 9 | HG01358.hp1 HG02602.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.3846-1525_3846-152 others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299695 | ||||||
| chr12:123299700
|
C | A | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3846-1529G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299700 | ||||||
| chr12:123299910
|
G | A | 1 | a0002c0004t0032g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3846-1739C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123299910 | ||||||
| chr12:123300292
|
C | T | 4 | a0001c0002t0009g0241a0001c0002t0009g0242a0001c0002t0088g0239others(1): Show | 4 | NA18981.hp2 NA18991.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.3846-2121G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300292 | ||||||
| chr12:123300383
|
C | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3846-2212G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300383 | ||||||
| chr12:123300423
|
A | C | 1 | a0001c0003t0030g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3846-2252T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300423 | ||||||
| chr12:123300454
|
A | C | 3 | a0001c0010t0060g0130a0001c0010t0061g0119a0001c0013t0070g0193 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3846-2283T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300454 | ||||||
| chr12:123300532
|
C | T | 1 | a0001c0005t0025g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3845+2292G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300532 | ||||||
| chr12:123300641
|
G | C | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3845+2183C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300641 | ||||||
| chr12:123300843
|
T | C | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3845+1981A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300843 | ||||||
| chr12:123300951
|
C | G | 1 | a0001c0003t0014g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3845+1873G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300951 | ||||||
| chr12:123300970
|
C | A | 1 | a0001c0011t0003g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3845+1854G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300970 | ||||||
| chr12:123300971
|
A | C | 1 | a0001c0011t0003g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3845+1853T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300971 | ||||||
| chr12:123300975
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3845+1849T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300975 | ||||||
| chr12:123300978
|
A | ACC | 38 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(35): Show | 38 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.3845+1845_3845+184 others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300978 | ||||||
| chr12:123300979
|
A | C | 27 | a0001c0005t0015g0205a0001c0005t0015g0206a0001c0005t0015g0207others(24): Show | 27 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.3845+1845T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300979 | ||||||
| chr12:123300980
|
C | A | 42 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(39): Show | 42 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.3845+1844G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300980 | ||||||
| chr12:123300980
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0197a0001c0001t0001g0202a0001c0001t0058g0196 | 3 | HG00741.hp2 HG01167.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.3845+1834_3845+184 others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300980 | ||||||
| chr12:123300991
|
C | A | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.3845+1833G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123300991 | ||||||
| chr12:123301333
|
G | T | 1 | a0001c0006t0010g0007 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3845+1491C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301333 | ||||||
| chr12:123301443
|
C | G | 2 | a0001c0002t0034g0217a0001c0002t0034g0218 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3845+1381G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301443 | ||||||
| chr12:123301514
|
G | T | 3 | a0001c0003t0005g0028a0001c0003t0005g0030a0001c0003t0005g0031 | 3 | HG01099.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.3845+1310C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301514 | ||||||
| chr12:123301697
|
T | A | 2 | a0001c0002t0034g0217a0001c0002t0034g0218 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3845+1127A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301697 | ||||||
| chr12:123301922
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3845+902C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301922 | ||||||
| chr12:123301941
|
G | GT | 7 | a0001c0001t0001g0125a0001c0001t0001g0182a0001c0001t0001g0199others(4): Show | 7 | HG01256.hp2 HG02809.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.3845+882dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301941 | ||||||
| chr12:123301941
|
G | T | 1 | a0001c0001t0029g0137 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3845+883C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301941 | ||||||
| chr12:123301944
|
TG | T | 42 | a0001c0001t0018g0211a0001c0002t0003g0219a0001c0002t0003g0224others(39): Show | 42 | HG00642.hp2 HG00673.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.3845+879delC | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301944 | ||||||
| chr12:123301945
|
G | T | 148 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(145): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.3845+879C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123301945 | ||||||
| chr12:123302249
|
TG | T | 19 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(16): Show | 19 | HG00280.hp2 HG01358.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.3845+574delC | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123302249 | ||||||
| chr12:123302250
|
G | T | 5 | a0001c0002t0009g0253a0001c0006t0010g0014a0001c0006t0011g0003others(2): Show | 5 | HG01175.hp2 HG02148.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3845+574C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123302250 | ||||||
| chr12:123302250
|
GT | G | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3845+573delA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123302250 | ||||||
| chr12:123302251
|
T | G | 1 | a0001c0002t0009g0253 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3845+573A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123302251 | ||||||
| chr12:123302346
|
G | C | 1 | a0001c0001t0013g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3845+478C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123302346 | ||||||
| chr12:123302537
|
C | T | 5 | a0001c0003t0066g0069a0001c0003t0071g0067a0001c0003t0072g0068others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3845+287G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123302537 | ||||||
| chr12:123302544
|
G | A | 11 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3845+280C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 30/31 | chr12 | 123302544 | ||||||
| chr12:123302924
|
T | C | 2 | a0001c0002t0003g0227a0001c0002t0003g0228 | 2 | HG01070.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3769-24A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123302924 | ||||||
| chr12:123302958
|
C | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3769-58G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123302958 | ||||||
| chr12:123303011
|
A | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3769-111T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303011 | ||||||
| chr12:123303183
|
T | A | 3 | a0002c0004t0002g0038a0002c0004t0002g0043a0002c0004t0002g0050 | 3 | HG03017.hp1 HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3769-283A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303183 | ||||||
| chr12:123303264
|
C | T | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.3769-364G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303264 | ||||||
| chr12:123303634
|
A | AAGGAGTC | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.3769-735_3769-734i others(9): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303634 | ||||||
| chr12:123303658
|
GTAACAT | G | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3769-764_3769-759d others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303658 | ||||||
| chr12:123303699
|
C | T | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.3769-799G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303699 | ||||||
| chr12:123303838
|
AAAAG | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3768+740_3768+743d others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303838 | ||||||
| chr12:123303911
|
A | C | 1 | a0001c0010t0061g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3768+671T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303911 | ||||||
| chr12:123303922
|
C | CT | 174 | a0001c0001t0001g0099a0001c0001t0001g0122a0001c0001t0001g0125others(171): Show | 174 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(171): Show |
intron_variant | MODIFIER | c.3768+659dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303922 | ||||||
| chr12:123303922
|
C | CTT | 19 | a0001c0001t0001g0126a0001c0001t0001g0149a0001c0001t0001g0154others(16): Show | 19 | HG00438.hp1 HG00438.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.3768+658_3768+659d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303922 | ||||||
| chr12:123303922
|
CTTT | C | 19 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(16): Show | 19 | HG01358.hp1 HG01943.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.3768+657_3768+659d others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303922 | ||||||
| chr12:123303947
|
G | C | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3768+635C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303947 | ||||||
| chr12:123303955
|
C | G | 1 | a0001c0003t0014g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3768+627G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303955 | ||||||
| chr12:123303995
|
C | T | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3768+587G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123303995 | ||||||
| chr12:123304002
|
C | G | 1 | a0001c0001t0007g0179 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3768+580G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123304002 | ||||||
| chr12:123304211
|
G | A | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.3768+371C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123304211 | ||||||
| chr12:123304255
|
A | T | 5 | a0001c0003t0066g0069a0001c0003t0071g0067a0001c0003t0072g0068others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3768+327T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123304255 | ||||||
| chr12:123304329
|
G | T | 1 | a0001c0003t0045g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3768+253C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123304329 | ||||||
| chr12:123304360
|
A | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3768+222T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123304360 | ||||||
| chr12:123304488
|
G | A | 1 | a0001c0005t0015g0206 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3768+94C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123304488 | ||||||
| chr12:123304509
|
T | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3768+73A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 29/31 | chr12 | 123304509 | ||||||
| chr12:123304827
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3631-108C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123304827 | ||||||
| chr12:123305396
|
A | C | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3631-677T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123305396 | ||||||
| chr12:123305460
|
T | C | 69 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(66): Show | 69 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.3631-741A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123305460 | ||||||
| chr12:123305504
|
T | C | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.3631-785A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123305504 | ||||||
| chr12:123305533
|
C | T | 1 | a0001c0002t0085g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3631-814G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123305533 | ||||||
| chr12:123305967
|
C | T | 1 | a0001c0015t0051g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3631-1248G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123305967 | ||||||
| chr12:123305991
|
T | G | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3631-1272A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123305991 | ||||||
| chr12:123306236
|
C | A | 9 | a0003c0007t0008g0001a0003c0007t0008g0016a0003c0007t0008g0017others(6): Show | 9 | HG01358.hp1 HG02602.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.3631-1517G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123306236 | ||||||
| chr12:123306249
|
C | T | 2 | a0001c0005t0025g0201a0001c0005t0048g0118 | 2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.3631-1530G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123306249 | ||||||
| chr12:123306618
|
C | G | 94 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.3631-1899G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123306618 | ||||||
| chr12:123306654
|
G | A | 6 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3631-1935C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123306654 | ||||||
| chr12:123306680
|
C | T | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.3631-1961G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123306680 | ||||||
| chr12:123306786
|
AAATATTA others(14): Show |
A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3631-2088_3631-206 others(25): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123306786 | ||||||
| chr12:123306869
|
C | T | 1 | a0001c0005t0025g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3631-2150G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123306869 | ||||||
| chr12:123306907
|
G | A | 3 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004 | 3 | HG01175.hp2 HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3631-2188C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123306907 | ||||||
| chr12:123307020
|
T | TA | 111 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0125others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.3630+2289dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAA | 7 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0199others(4): Show | 7 | HG00642.hp2 HG02165.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.3630+2288_3630+228 others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAA | 16 | a0001c0006t0010g0009a0001c0006t0010g0011a0001c0006t0010g0013others(13): Show | 16 | HG00280.hp2 HG01358.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.3630+2286_3630+228 others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAA | 10 | a0001c0002t0009g0241a0001c0002t0009g0242a0001c0002t0009g0243others(7): Show | 10 | HG00621.hp1 HG02071.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.3630+2285_3630+228 others(9): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAAAA others(10): Show |
12 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0227others(9): Show | 12 | HG01070.hp2 HG02155.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.3630+2273_3630+228 others(21): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAAAA others(11): Show |
5 | a0001c0002t0003g0225a0001c0002t0003g0231a0001c0002t0003g0233others(2): Show | 5 | HG00673.hp1 NA18948.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.3630+2272_3630+228 others(22): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAAAA others(12): Show |
3 | a0001c0002t0003g0232a0001c0002t0089g0247a0001c0002t0090g0222 | 3 | HG02738.hp2 NA18942.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3630+2271_3630+228 others(23): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAAAA others(13): Show |
4 | a0001c0002t0003g0246a0001c0002t0003g0249a0001c0002t0022g0230others(1): Show | 4 | HG02080.hp1 NA18993.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.3630+2270_3630+228 others(24): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAAAA others(14): Show |
1 | a0001c0002t0092g0226 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3630+2269_3630+228 others(25): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAAAA others(16): Show |
1 | a0001c0002t0003g0248 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3630+2289_3630+229 others(27): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAAAA others(19): Show |
1 | a0001c0002t0091g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3630+2289_3630+229 others(30): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TAAAAAAA others(26): Show |
1 | a0001c0002t0095g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3630+2289_3630+229 others(37): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
T | TTAAAA | 4 | a0001c0006t0010g0007a0001c0006t0011g0002a0001c0006t0011g0004others(1): Show | 4 | HG02683.hp1 HG03471.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.3630+2289_3630+229 others(9): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307020
|
TA | T | 5 | a0001c0002t0034g0217a0001c0002t0034g0218a0001c0003t0019g0080others(2): Show | 5 | HG01070.hp1 HG01243.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3630+2289delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307020 | ||||||
| chr12:123307063
|
C | T | 1 | a0001c0003t0076g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3630+2247G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307063 | ||||||
| chr12:123307102
|
T | C | 19 | a0001c0008t0006g0113a0002c0004t0002g0038a0002c0004t0002g0040others(16): Show | 19 | HG00140.hp2 HG00738.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.3630+2208A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307102 | ||||||
| chr12:123307145
|
C | T | 1 | a0001c0012t0050g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3630+2165G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307145 | ||||||
| chr12:123307311
|
A | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3630+1999T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307311 | ||||||
| chr12:123307409
|
C | T | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3630+1901G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307409 | ||||||
| chr12:123307489
|
A | T | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3630+1821T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307489 | ||||||
| chr12:123307490
|
T | G | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3630+1820A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307490 | ||||||
| chr12:123307655
|
G | A | 1 | a0001c0002t0009g0253 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3630+1655C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307655 | ||||||
| chr12:123307874
|
C | G | 1 | a0001c0003t0005g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3630+1436G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307874 | ||||||
| chr12:123307918
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3630+1392C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123307918 | ||||||
| chr12:123308003
|
C | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3630+1307G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123308003 | ||||||
| chr12:123308138
|
T | C | 2 | a0001c0001t0004g0212a0001c0001t0018g0211 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3630+1172A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123308138 | ||||||
| chr12:123308154
|
T | C | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3630+1156A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123308154 | ||||||
| chr12:123308225
|
A | G | 1 | a0001c0003t0005g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3630+1085T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123308225 | ||||||
| chr12:123308301
|
C | A | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.3630+1009G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123308301 | ||||||
| chr12:123308368
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3630+942A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123308368 | ||||||
| chr12:123309067
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3630+243C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123309067 | ||||||
| chr12:123309084
|
AAAG | A | 92 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.3630+223_3630+225d others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123309084 | ||||||
| chr12:123309113
|
A | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3630+197T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 28/31 | chr12 | 123309113 | ||||||
| chr12:123309475
|
T | C | 241 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.3537+14A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 27/31 | chr12 | 123309475 | ||||||
| chr12:123309903
|
A | T | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.3296-47T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123309903 | ||||||
| chr12:123310010
|
C | G | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.3296-154G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310010 | ||||||
| chr12:123310022
|
T | C | 1 | a0001c0001t0013g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3296-166A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310022 | ||||||
| chr12:123310034
|
A | C | 94 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.3296-178T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310034 | ||||||
| chr12:123310040
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0125 | 2 | HG03491.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.3296-184G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310040 | ||||||
| chr12:123310299
|
T | TCCTGGCT others(9): Show |
1 | a0001c0003t0073g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3296-444_3296-443i others(18): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310299 | ||||||
| chr12:123310302
|
T | C | 1 | a0001c0003t0073g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3296-446A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310302 | ||||||
| chr12:123310322
|
C | A | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3296-466G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310322 | ||||||
| chr12:123310324
|
G | C | 190 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(187): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.3296-468C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310324 | ||||||
| chr12:123310378
|
C | T | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.3296-522G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310378 | ||||||
| chr12:123310383
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3296-527C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310383 | ||||||
| chr12:123310409
|
T | C | 3 | a0001c0005t0015g0205a0001c0005t0015g0206a0001c0005t0015g0207 | 3 | HG02451.hp1 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3296-553A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310409 | ||||||
| chr12:123310732
|
A | G | 1 | a0001c0008t0006g0095 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3295+323T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310732 | ||||||
| chr12:123310823
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3295+232C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123310823 | ||||||
| chr12:123311017
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3295+38C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123311017 | ||||||
| chr12:123311033
|
C | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3295+22G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 25/31 | chr12 | 123311033 | ||||||
| chr12:123311208
|
G | T | 1 | a0001c0001t0063g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3221-79C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311208 | ||||||
| chr12:123311212
|
G | C | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3221-83C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311212 | ||||||
| chr12:123311544
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3221-415C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311544 | ||||||
| chr12:123311644
|
T | C | 3 | a0001c0003t0005g0028a0001c0003t0005g0030a0001c0003t0005g0031 | 3 | HG01099.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.3221-515A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311644 | ||||||
| chr12:123311689
|
A | AATCAATC others(5): Show |
1 | a0001c0006t0011g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3221-561_3221-560i others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311689 | ||||||
| chr12:123311689
|
AACCT | A | 5 | a0001c0006t0010g0009a0001c0006t0010g0014a0001c0006t0038g0010others(2): Show | 5 | HG01358.hp1 HG01952.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.3221-564_3221-561d others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311689 | ||||||
| chr12:123311691
|
C | CCTAT | 19 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0149others(16): Show | 19 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.3221-566_3221-563d others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311691 | ||||||
| chr12:123311691
|
C | CCTATCTA others(1): Show |
9 | a0001c0001t0001g0120a0001c0001t0001g0155a0001c0001t0001g0160others(6): Show | 9 | HG01243.hp1 HG01358.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3221-570_3221-563d others(10): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311691 | ||||||
| chr12:123311691
|
C | CCTATCTA others(5): Show |
2 | a0001c0001t0007g0200a0001c0001t0018g0211 | 2 | HG01516.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.3221-574_3221-563d others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311691 | ||||||
| chr12:123311691
|
C | T | 63 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(60): Show | 63 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.3221-562G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311691 | ||||||
| chr12:123311712
|
CTATCTAT others(3): Show |
C | 1 | a0001c0003t0065g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3221-593_3221-584d others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311712 | ||||||
| chr12:123311716
|
C | CTA | 4 | a0001c0001t0004g0121a0001c0003t0005g0031a0004c0009t0062g0087others(1): Show | 4 | HG02280.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3221-589_3221-588d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311716 | ||||||
| chr12:123311716
|
CTATCTAT others(11): Show |
C | 1 | a0001c0001t0001g0162 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3221-605_3221-588d others(20): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311716 | ||||||
| chr12:123311720
|
C | A | 9 | a0001c0001t0004g0121a0001c0003t0005g0028a0001c0003t0005g0031others(6): Show | 9 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3221-591G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTA | 4 | a0001c0001t0001g0166a0001c0001t0028g0152a0001c0003t0074g0083others(1): Show | 4 | HG01081.hp2 HG01928.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3221-593_3221-592d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATATAT others(3): Show |
1 | a0001c0005t0048g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3221-601_3221-592d others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATATAT others(7): Show |
1 | a0001c0005t0015g0205 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3221-605_3221-592d others(16): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATATAT others(9): Show |
1 | a0001c0005t0025g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3221-607_3221-592d others(18): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATATAT others(11): Show |
1 | a0001c0010t0060g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3221-609_3221-592d others(20): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATCTA | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0003t0067g0066others(1): Show | 4 | HG03209.hp2 NA18952.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.3221-592_3221-591i others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATCTAT others(1): Show |
3 | a0001c0003t0014g0074a0001c0005t0006g0105a0001c0012t0050g0123 | 3 | HG02809.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3221-592_3221-591i others(10): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATCTAT others(3): Show |
2 | a0001c0005t0015g0206a0001c0005t0025g0094 | 2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3221-592_3221-591i others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATCTAT others(7): Show |
1 | a0001c0003t0014g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3221-592_3221-591i others(16): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATCTAT others(3): Show |
3 | a0001c0001t0001g0198a0001c0003t0019g0064a0001c0010t0061g0119 | 3 | HG02922.hp2 NA19005.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3221-592_3221-591i others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
C | CTATCTAT others(7): Show |
2 | a0001c0001t0013g0192a0001c0003t0077g0063 | 2 | HG01884.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3221-592_3221-591i others(16): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
CTA | C | 14 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0163others(11): Show | 14 | HG00735.hp2 HG02109.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.3221-593_3221-592d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
CTATATA | C | 3 | a0001c0001t0033g0167a0001c0001t0033g0186a0002c0004t0002g0053 | 3 | HG03490.hp2 HG03492.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3221-597_3221-592d others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
CTATATAT others(1): Show |
C | 10 | a0001c0006t0010g0007a0001c0006t0011g0023a0003c0007t0008g0001others(7): Show | 10 | HG02602.hp1 HG03471.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.3221-599_3221-592d others(10): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
CTATATAT others(3): Show |
C | 30 | a0002c0004t0002g0038a0002c0004t0002g0040a0002c0004t0002g0043others(27): Show | 30 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.3221-601_3221-592d others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
CTATATAT others(7): Show |
C | 4 | a0001c0002t0003g0227a0001c0002t0003g0228a0001c0002t0086g0220others(1): Show | 4 | HG01070.hp2 HG02293.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.3221-605_3221-592d others(16): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311720
|
CTATATAT others(11): Show |
C | 37 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(34): Show | 37 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.3221-609_3221-592d others(20): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311720 | ||||||
| chr12:123311722
|
A | ATC | 20 | a0001c0001t0001g0122a0001c0001t0001g0159a0001c0001t0001g0169others(17): Show | 20 | HG00280.hp1 HG01074.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.3221-594_3221-593i others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311722 | ||||||
| chr12:123311722
|
A | ATCTATC | 24 | a0001c0001t0001g0099a0001c0001t0001g0138a0001c0001t0001g0175others(21): Show | 24 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.3221-594_3221-593i others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311722 | ||||||
| chr12:123311722
|
A | ATCTATCT others(3): Show |
9 | a0001c0001t0001g0183a0001c0001t0001g0197a0001c0001t0054g0164others(6): Show | 9 | HG00741.hp2 HG01099.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.3221-594_3221-593i others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311722 | ||||||
| chr12:123311724
|
A | C | 49 | a0001c0001t0001g0126a0001c0001t0001g0134a0001c0001t0001g0135others(46): Show | 49 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.3221-595T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311724 | ||||||
| chr12:123311726
|
A | C | 25 | a0001c0001t0001g0125a0001c0001t0001g0159a0001c0001t0001g0161others(22): Show | 25 | HG00741.hp2 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3221-597T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311726 | ||||||
| chr12:123311728
|
A | C | 28 | a0001c0001t0001g0149a0001c0001t0001g0199a0001c0001t0004g0210others(25): Show | 28 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.3221-599T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311728 | ||||||
| chr12:123311730
|
A | C | 12 | a0001c0001t0001g0161a0001c0001t0001g0173a0001c0001t0001g0202others(9): Show | 12 | HG01175.hp1 HG01243.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.3221-601T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311730 | ||||||
| chr12:123311732
|
A | C | 27 | a0001c0001t0004g0210a0001c0001t0004g0213a0001c0001t0004g0214others(24): Show | 27 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.3221-603T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311732 | ||||||
| chr12:123311734
|
A | C | 6 | a0001c0001t0001g0161a0001c0001t0001g0173a0001c0002t0034g0217others(3): Show | 6 | HG01243.hp2 HG02300.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3221-605T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311734 | ||||||
| chr12:123311736
|
A | C | 20 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(17): Show | 20 | HG00280.hp2 HG01358.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.3221-607T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311736 | ||||||
| chr12:123311738
|
A | C | 7 | a0001c0002t0003g0227a0001c0002t0003g0228a0001c0002t0034g0217others(4): Show | 7 | HG01070.hp2 HG01243.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.3221-609T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311738 | ||||||
| chr12:123311740
|
A | C | 2 | a0001c0014t0036g0008a0003c0007t0008g0001 | 2 | HG02132.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.3221-611T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311740 | ||||||
| chr12:123311746
|
A | T | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3221-617T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311746 | ||||||
| chr12:123311748
|
A | T | 3 | a0001c0003t0014g0074a0001c0003t0014g0076a0001c0013t0070g0193 | 3 | HG02451.hp2 HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3221-619T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311748 | ||||||
| chr12:123311750
|
T | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0202a0001c0001t0017g0136others(1): Show | 4 | HG00741.hp2 HG01167.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.3221-621A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123311750 | ||||||
| chr12:123312081
|
CT | C | 70 | a0001c0001t0056g0157a0001c0001t0058g0196a0001c0002t0003g0219others(67): Show | 70 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.3221-953delA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312081 | ||||||
| chr12:123312152
|
AC | A | 3 | a0001c0010t0060g0130a0001c0010t0061g0119a0001c0013t0070g0193 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3221-1024delG | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312152 | ||||||
| chr12:123312215
|
C | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3221-1086G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312215 | ||||||
| chr12:123312288
|
G | A | 1 | a0001c0003t0044g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3221-1159C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312288 | ||||||
| chr12:123312300
|
T | C | 1 | a0001c0003t0005g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3221-1171A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312300 | ||||||
| chr12:123312302
|
C | T | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.3221-1173G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312302 | ||||||
| chr12:123312450
|
A | G | 67 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(64): Show | 67 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.3220+1170T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312450 | ||||||
| chr12:123312469
|
T | C | 2 | a0001c0001t0027g0093a0001c0001t0027g0165 | 2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.3220+1151A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312469 | ||||||
| chr12:123312664
|
T | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3220+956A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312664 | ||||||
| chr12:123312668
|
A | G | 4 | a0001c0008t0006g0095a0001c0008t0006g0113a0001c0008t0024g0100others(1): Show | 4 | HG02055.hp1 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3220+952T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312668 | ||||||
| chr12:123312711
|
GA | G | 41 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(38): Show | 41 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.3220+908delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123312711 | ||||||
| chr12:123313020
|
T | C | 92 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.3220+600A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313020 | ||||||
| chr12:123313201
|
A | AAAAT | 12 | a0001c0001t0007g0147a0001c0001t0007g0179a0001c0001t0083g0124others(9): Show | 12 | HG01074.hp2 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.3220+415_3220+418d others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313201 | ||||||
| chr12:123313201
|
AAAAT | A | 57 | a0001c0001t0001g0145a0001c0001t0001g0159a0001c0001t0001g0166others(54): Show | 57 | HG00280.hp2 HG00639.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.3220+415_3220+418d others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313201 | ||||||
| chr12:123313201
|
AAAATAAA others(1): Show |
A | 41 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0135others(38): Show | 41 | HG00642.hp2 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.3220+411_3220+418d others(10): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313201 | ||||||
| chr12:123313201
|
AAAATAAA others(5): Show |
A | 38 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0227others(35): Show | 38 | HG00621.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.3220+407_3220+418d others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313201 | ||||||
| chr12:123313201
|
AAAATAAA others(9): Show |
A | 5 | a0001c0001t0057g0131a0001c0005t0025g0201a0001c0005t0048g0118others(2): Show | 5 | HG01074.hp1 HG01109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3220+403_3220+418d others(18): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313201 | ||||||
| chr12:123313201
|
AAAATAAA others(21): Show |
A | 1 | a0001c0002t0085g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3220+391_3220+418d others(30): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313201 | ||||||
| chr12:123313252
|
A | T | 1 | a0001c0002t0003g0219 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3220+368T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313252 | ||||||
| chr12:123313287
|
A | T | 1 | a0001c0003t0030g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3220+333T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313287 | ||||||
| chr12:123313314
|
T | A | 1 | a0003c0007t0008g0018 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3220+306A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313314 | ||||||
| chr12:123313427
|
C | G | 1 | a0003c0007t0041g0019 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3220+193G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313427 | ||||||
| chr12:123313527
|
A | G | 9 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(6): Show | 9 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.3220+93T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313527 | ||||||
| chr12:123313586
|
C | G | 4 | a0001c0001t0001g0145a0001c0001t0004g0121a0001c0001t0028g0152others(1): Show | 4 | HG01928.hp2 HG02293.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.3220+34G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313586 | ||||||
| chr12:123313597
|
T | G | 1 | a0001c0005t0012g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3220+23A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 24/31 | chr12 | 123313597 | ||||||
| chr12:123313723
|
CA | C | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
splice_region_variant&intron_variant | LOW | c.3121-5delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123313723 | ||||||
| chr12:123313805
|
C | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3121-86G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123313805 | ||||||
| chr12:123313835
|
T | C | 1 | a0001c0006t0011g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3121-116A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123313835 | ||||||
| chr12:123313877
|
T | C | 1 | a0002c0004t0020g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3121-158A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123313877 | ||||||
| chr12:123314270
|
G | A | 1 | a0001c0006t0038g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3121-551C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314270 | ||||||
| chr12:123314334
|
A | AT | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.3121-616dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314334 | ||||||
| chr12:123314334
|
A | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3121-615T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314334 | ||||||
| chr12:123314531
|
T | C | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3121-812A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314531 | ||||||
| chr12:123314606
|
C | T | 1 | a0001c0010t0060g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3120+767G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314606 | ||||||
| chr12:123314830
|
C | T | 1 | a0001c0010t0061g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3120+543G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314830 | ||||||
| chr12:123314892
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0183a0001c0001t0001g0190 | 3 | HG00639.hp1 HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3120+481C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314892 | ||||||
| chr12:123314906
|
A | AT | 5 | a0001c0002t0003g0238a0001c0002t0034g0218a0001c0002t0085g0209others(2): Show | 5 | HG01069.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3120+466dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314906 | ||||||
| chr12:123314906
|
A | ATT | 38 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(35): Show | 38 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.3120+465_3120+466d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314906 | ||||||
| chr12:123314991
|
C | T | 1 | a0001c0006t0010g0009 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3120+382G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123314991 | ||||||
| chr12:123315089
|
A | T | 2 | a0001c0001t0004g0212a0001c0001t0018g0211 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3120+284T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123315089 | ||||||
| chr12:123315184
|
T | C | 1 | a0001c0002t0021g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3120+189A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 23/31 | chr12 | 123315184 | ||||||
| chr12:123315829
|
A | G | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2936-169T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123315829 | ||||||
| chr12:123316000
|
G | A | 1 | a0003c0007t0041g0019 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2936-340C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316000 | ||||||
| chr12:123316149
|
CATATACT | C | 10 | a0001c0003t0023g0024a0001c0005t0006g0104a0001c0005t0006g0105others(7): Show | 10 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2936-496_2936-490d others(9): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316149 | ||||||
| chr12:123316205
|
G | T | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2936-545C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316205 | ||||||
| chr12:123316273
|
A | G | 190 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(187): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2936-613T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316273 | ||||||
| chr12:123316318
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2936-658C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316318 | ||||||
| chr12:123316386
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2936-726C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316386 | ||||||
| chr12:123316503
|
C | T | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2935+718G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316503 | ||||||
| chr12:123316513
|
T | C | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2935+708A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316513 | ||||||
| chr12:123316694
|
TTTC | T | 5 | a0001c0002t0003g0227a0001c0002t0003g0229a0001c0002t0022g0230others(2): Show | 5 | HG01070.hp2 HG02970.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2935+524_2935+526d others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316694 | ||||||
| chr12:123316701
|
TTC | T | 39 | a0001c0002t0003g0224a0001c0002t0003g0225a0001c0002t0003g0228others(36): Show | 39 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.2935+518_2935+519d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316701 | ||||||
| chr12:123316703
|
C | CT | 117 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2935+517dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316703 | ||||||
| chr12:123316758
|
A | G | 2 | a0001c0001t0004g0212a0001c0001t0018g0211 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2935+463T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316758 | ||||||
| chr12:123316764
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2935+457C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316764 | ||||||
| chr12:123316810
|
C | T | 2 | a0002c0004t0002g0046a0002c0004t0002g0048 | 2 | HG01081.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2935+411G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316810 | ||||||
| chr12:123316947
|
C | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2935+274G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123316947 | ||||||
| chr12:123317125
|
T | G | 190 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(187): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2935+96A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 21/31 | chr12 | 123317125 | ||||||
| chr12:123317393
|
A | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2800-37T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123317393 | ||||||
| chr12:123317454
|
T | C | 1 | a0002c0004t0002g0059 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2800-98A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123317454 | ||||||
| chr12:123317582
|
A | G | 1 | a0002c0004t0002g0059 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2800-226T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123317582 | ||||||
| chr12:123317648
|
G | A | 1 | a0001c0005t0025g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2800-292C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123317648 | ||||||
| chr12:123317779
|
G | A | 1 | a0001c0003t0067g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2800-423C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123317779 | ||||||
| chr12:123317785
|
T | C | 4 | a0001c0005t0012g0110a0001c0005t0012g0111a0001c0005t0012g0114others(1): Show | 4 | HG02109.hp1 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2800-429A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123317785 | ||||||
| chr12:123318014
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2800-658A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318014 | ||||||
| chr12:123318143
|
A | G | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2800-787T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318143 | ||||||
| chr12:123318267
|
T | C | 68 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(65): Show | 68 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.2800-911A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318267 | ||||||
| chr12:123318540
|
C | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2800-1184G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318540 | ||||||
| chr12:123318737
|
C | CAA | 38 | a0001c0002t0003g0219a0001c0002t0003g0225a0001c0002t0003g0227others(35): Show | 38 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.2799+1161_2799+116 others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318737 | ||||||
| chr12:123318737
|
C | CAAA | 5 | a0001c0002t0003g0224a0001c0002t0003g0249a0001c0002t0009g0243others(2): Show | 5 | HG02071.hp2 HG02080.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.2799+1160_2799+116 others(7): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318737 | ||||||
| chr12:123318737
|
CA | C | 116 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2799+1162delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318737 | ||||||
| chr12:123318865
|
CAG | C | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.2799+1033_2799+103 others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318865 | ||||||
| chr12:123318922
|
C | T | 4 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004others(1): Show | 4 | HG01175.hp2 HG02683.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2799+978G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318922 | ||||||
| chr12:123318967
|
G | GT | 23 | a0001c0001t0001g0155a0001c0001t0001g0161a0001c0001t0001g0173others(20): Show | 23 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2799+932dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318967 | ||||||
| chr12:123318967
|
GT | G | 27 | a0001c0005t0006g0109a0001c0005t0006g0115a0001c0005t0046g0102others(24): Show | 27 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.2799+932delA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123318967 | ||||||
| chr12:123319124
|
C | T | 1 | a0001c0001t0007g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2799+776G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319124 | ||||||
| chr12:123319165
|
CCAT | C | 3 | a0001c0010t0060g0130a0001c0010t0061g0119a0001c0013t0070g0193 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2799+732_2799+734d others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319165 | ||||||
| chr12:123319188
|
A | C | 1 | a0002c0004t0002g0047 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2799+712T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319188 | ||||||
| chr12:123319216
|
C | T | 1 | a0002c0004t0002g0040 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2799+684G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319216 | ||||||
| chr12:123319333
|
G | A | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2799+567C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319333 | ||||||
| chr12:123319342
|
C | T | 2 | a0001c0001t0004g0132a0001c0001t0004g0143 | 2 | HG00140.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2799+558G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319342 | ||||||
| chr12:123319476
|
C | G | 1 | a0003c0007t0008g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2799+424G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319476 | ||||||
| chr12:123319567
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2799+333G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319567 | ||||||
| chr12:123319581
|
G | A | 1 | a0001c0012t0050g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2799+319C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319581 | ||||||
| chr12:123319643
|
A | G | 4 | a0001c0005t0006g0109a0001c0005t0006g0115a0001c0005t0046g0102others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2799+257T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319643 | ||||||
| chr12:123319843
|
T | C | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2799+57A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 20/31 | chr12 | 123319843 | ||||||
| chr12:123320174
|
G | C | 68 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(65): Show | 68 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.2668-143C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 19/31 | chr12 | 123320174 | ||||||
| chr12:123320192
|
T | G | 1 | a0001c0012t0050g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2668-161A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 19/31 | chr12 | 123320192 | ||||||
| chr12:123320205
|
C | T | 1 | a0002c0004t0002g0055 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2668-174G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 19/31 | chr12 | 123320205 | ||||||
| chr12:123320224
|
A | G | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2668-193T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 19/31 | chr12 | 123320224 | ||||||
| chr12:123320634
|
T | C | 1 | a0001c0002t0003g0259 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2492-27A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 18/31 | chr12 | 123320634 | ||||||
| chr12:123321082
|
G | C | 22 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(19): Show | 22 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.2324-216C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 17/31 | chr12 | 123321082 | ||||||
| chr12:123321285
|
G | C | 1 | a0001c0010t0060g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2323+250C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 17/31 | chr12 | 123321285 | ||||||
| chr12:123321403
|
G | A | 4 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004others(1): Show | 4 | HG01175.hp2 HG02683.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2323+132C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 17/31 | chr12 | 123321403 | ||||||
| chr12:123321736
|
C | T | 3 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106 | 3 | HG01243.hp1 HG02647.hp1 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.2126-4G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123321736 | ||||||
| chr12:123321916
|
G | A | 2 | a0001c0001t0029g0133a0001c0001t0029g0137 | 2 | NA19003.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2126-184C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123321916 | ||||||
| chr12:123321917
|
T | G | 1 | a0002c0004t0002g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2126-185A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123321917 | ||||||
| chr12:123322119
|
T | C | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2126-387A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322119 | ||||||
| chr12:123322195
|
C | G | 1 | a0002c0004t0020g0078 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2126-463G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322195 | ||||||
| chr12:123322201
|
T | C | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2126-469A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322201 | ||||||
| chr12:123322361
|
C | T | 3 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004 | 3 | HG01175.hp2 HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2126-629G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322361 | ||||||
| chr12:123322418
|
C | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2126-686G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322418 | ||||||
| chr12:123322471
|
A | T | 44 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(41): Show | 44 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2126-739T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322471 | ||||||
| chr12:123322490
|
G | A | 6 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2126-758C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322490 | ||||||
| chr12:123322566
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2126-834C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322566 | ||||||
| chr12:123322577
|
G | T | 1 | a0003c0007t0008g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2126-845C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322577 | ||||||
| chr12:123322703
|
T | C | 240 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(237): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2126-971A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322703 | ||||||
| chr12:123322703
|
T | G | 1 | a0001c0001t0007g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2126-971A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322703 | ||||||
| chr12:123322815
|
G | C | 4 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004others(1): Show | 4 | HG01175.hp2 HG02683.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+865C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322815 | ||||||
| chr12:123322884
|
AAAAAAAA others(3): Show |
A | 43 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.2125+786_2125+795d others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322884 | ||||||
| chr12:123322998
|
A | G | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2125+682T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123322998 | ||||||
| chr12:123323009
|
A | T | 1 | a0001c0001t0004g0213 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2125+671T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123323009 | ||||||
| chr12:123323508
|
C | A | 1 | a0003c0007t0008g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2125+172G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123323508 | ||||||
| chr12:123323509
|
G | A | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2125+171C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123323509 | ||||||
| chr12:123323526
|
T | C | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.2125+154A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 16/31 | chr12 | 123323526 | ||||||
| chr12:123323890
|
G | T | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1974-59C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123323890 | ||||||
| chr12:123323901
|
T | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG01928.hp1 HG02080.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1974-70A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123323901 | ||||||
| chr12:123323905
|
T | C | 1 | a0001c0005t0006g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1974-74A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123323905 | ||||||
| chr12:123324205
|
C | CCAGTCAT others(12): Show |
3 | a0001c0010t0060g0130a0001c0010t0061g0119a0001c0013t0070g0193 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1974-393_1974-375d others(21): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324205 | ||||||
| chr12:123324324
|
C | CT | 5 | a0001c0002t0003g0228a0001c0002t0009g0242a0001c0002t0091g0223others(2): Show | 5 | HG02293.hp2 NA18949.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1974-494dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324324 | ||||||
| chr12:123324324
|
CTT | C | 206 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(203): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1974-495_1974-494d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324324 | ||||||
| chr12:123324324
|
CTTT | C | 5 | a0001c0003t0014g0076a0001c0005t0047g0103a0002c0004t0031g0052others(2): Show | 5 | HG00140.hp2 HG01109.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1974-496_1974-494d others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324324 | ||||||
| chr12:123324331
|
T | C | 9 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(6): Show | 9 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1974-500A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324331 | ||||||
| chr12:123324385
|
C | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1974-554G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324385 | ||||||
| chr12:123324510
|
C | T | 1 | a0001c0006t0010g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1974-679G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324510 | ||||||
| chr12:123324522
|
G | A | 2 | a0001c0001t0007g0140a0001c0001t0007g0180 | 2 | NA19056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1974-691C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324522 | ||||||
| chr12:123324579
|
C | T | 1 | a0002c0004t0002g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1974-748G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324579 | ||||||
| chr12:123324724
|
C | T | 1 | a0001c0003t0005g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1973+778G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324724 | ||||||
| chr12:123324949
|
C | T | 1 | a0001c0005t0025g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1973+553G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123324949 | ||||||
| chr12:123325251
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1973+251C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123325251 | ||||||
| chr12:123325271
|
C | T | 2 | a0001c0006t0037g0006a0001c0006t0038g0010 | 2 | NA18972.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1973+231G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123325271 | ||||||
| chr12:123325298
|
T | C | 1 | a0002c0004t0002g0059 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1973+204A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 15/31 | chr12 | 123325298 | ||||||
| chr12:123325662
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1876-63A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 14/31 | chr12 | 123325662 | ||||||
| chr12:123325776
|
AATTTAGG | A | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1876-184_1876-178d others(9): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 14/31 | chr12 | 123325776 | ||||||
| chr12:123325824
|
C | T | 1 | a0001c0002t0003g0225 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1876-225G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 14/31 | chr12 | 123325824 | ||||||
| chr12:123325828
|
T | G | 22 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(19): Show | 22 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1876-229A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 14/31 | chr12 | 123325828 | ||||||
| chr12:123325878
|
C | T | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1875+274G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 14/31 | chr12 | 123325878 | ||||||
| chr12:123325915
|
T | C | 9 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(6): Show | 9 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1875+237A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 14/31 | chr12 | 123325915 | ||||||
| chr12:123326115
|
A | AC | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1875+36dupG | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 14/31 | chr12 | 123326115 | ||||||
| chr12:123326455
|
T | C | 2 | a0003c0007t0008g0020a0003c0007t0008g0021 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1693-121A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123326455 | ||||||
| chr12:123326678
|
C | A | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1693-344G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123326678 | ||||||
| chr12:123326778
|
T | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1693-444A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123326778 | ||||||
| chr12:123326814
|
A | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1693-480T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123326814 | ||||||
| chr12:123326824
|
G | A | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1693-490C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123326824 | ||||||
| chr12:123326951
|
A | C | 1 | a0001c0001t0001g0198 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1692+475T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123326951 | ||||||
| chr12:123327001
|
TTTTTTG | T | 9 | a0003c0007t0008g0001a0003c0007t0008g0016a0003c0007t0008g0017others(6): Show | 9 | HG01358.hp1 HG02602.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.1692+419_1692+424d others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123327001 | ||||||
| chr12:123327035
|
T | A | 1 | a0001c0003t0005g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1692+391A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123327035 | ||||||
| chr12:123327137
|
G | T | 23 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(20): Show | 23 | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1692+289C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123327137 | ||||||
| chr12:123327181
|
T | C | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1692+245A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123327181 | ||||||
| chr12:123327225
|
G | C | 6 | a0001c0001t0001g0120a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG00438.hp1 HG01928.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.1692+201C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123327225 | ||||||
| chr12:123327353
|
G | A | 25 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(22): Show | 25 | HG01099.hp1 HG01243.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1692+73C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 13/31 | chr12 | 123327353 | ||||||
| chr12:123327582
|
G | A | 2 | a0001c0003t0043g0035a0001c0003t0044g0034 | 2 | HG02818.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.1539-3C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 12/31 | chr12 | 123327582 | ||||||
| chr12:123327642
|
G | A | 1 | a0001c0005t0025g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1539-63C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 12/31 | chr12 | 123327642 | ||||||
| chr12:123327650
|
G | T | 4 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004others(1): Show | 4 | HG01175.hp2 HG02683.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1538+57C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 12/31 | chr12 | 123327650 | ||||||
| chr12:123327660
|
C | T | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1538+47G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 12/31 | chr12 | 123327660 | ||||||
| chr12:123328064
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1297-37T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/31 | chr12 | 123328064 | ||||||
| chr12:123328082
|
G | C | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1297-55C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/31 | chr12 | 123328082 | ||||||
| chr12:123328216
|
C | T | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1297-189G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/31 | chr12 | 123328216 | ||||||
| chr12:123328240
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1297-213T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/31 | chr12 | 123328240 | ||||||
| chr12:123328459
|
T | C | 1 | a0001c0006t0010g0007 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1296+275A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/31 | chr12 | 123328459 | ||||||
| chr12:123328524
|
C | T | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1296+210G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/31 | chr12 | 123328524 | ||||||
| chr12:123328551
|
T | C | 1 | a0001c0003t0065g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1296+183A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/31 | chr12 | 123328551 | ||||||
| chr12:123328665
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1296+69G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 10/31 | chr12 | 123328665 | ||||||
| chr12:123328946
|
C | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1135-51G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123328946 | ||||||
| chr12:123329060
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1135-165T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123329060 | ||||||
| chr12:123329374
|
CT | C | 37 | a0001c0001t0001g0168a0001c0002t0003g0227a0001c0002t0003g0248others(34): Show | 37 | HG01070.hp2 HG01099.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1135-480delA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123329374 | ||||||
| chr12:123329595
|
T | TA | 11 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1135-701dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123329595 | ||||||
| chr12:123329844
|
C | A | 38 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(35): Show | 38 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.1134+575G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123329844 | ||||||
| chr12:123329919
|
T | C | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1134+500A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123329919 | ||||||
| chr12:123329920
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1134+499A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123329920 | ||||||
| chr12:123329990
|
A | T | 1 | a0001c0001t0004g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1134+429T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123329990 | ||||||
| chr12:123330304
|
A | G | 3 | a0001c0003t0014g0074a0001c0003t0014g0075a0001c0003t0014g0076 | 3 | HG01891.hp2 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1134+115T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 9/31 | chr12 | 123330304 | ||||||
| chr12:123330599
|
TA | T | 209 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1044-91delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 8/31 | chr12 | 123330599 | ||||||
| chr12:123330599
|
TAA | T | 6 | a0001c0001t0001g0153a0001c0001t0057g0131a0001c0003t0005g0025others(3): Show | 6 | HG01074.hp1 HG02258.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044-92_1044-91del others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 8/31 | chr12 | 123330599 | ||||||
| chr12:123330646
|
CA | C | 259 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(256): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1044-138delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 8/31 | chr12 | 123330646 | ||||||
| chr12:123330833
|
C | G | 5 | a0001c0003t0030g0085a0001c0003t0030g0090a0001c0003t0064g0086others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044-324G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 8/31 | chr12 | 123330833 | ||||||
| chr12:123330925
|
G | A | 1 | a0001c0010t0061g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1043+317C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 8/31 | chr12 | 123330925 | ||||||
| chr12:123331009
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1043+233G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 8/31 | chr12 | 123331009 | ||||||
| chr12:123331107
|
A | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1043+135T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 8/31 | chr12 | 123331107 | ||||||
| chr12:123331121
|
A | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1043+121T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 8/31 | chr12 | 123331121 | ||||||
| chr12:123331392
|
T | A | 3 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004 | 3 | HG01175.hp2 HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.910-17A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331392 | ||||||
| chr12:123331460
|
T | TATGTTG | 209 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.910-86_910-85insCA others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331460 | ||||||
| chr12:123331465
|
T | TG | 5 | a0001c0005t0012g0110a0001c0005t0012g0111a0001c0005t0012g0114others(2): Show | 5 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-91_910-90insC | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331465 | ||||||
| chr12:123331469
|
TTTTTTGT others(6): Show |
T | 1 | a0001c0005t0025g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.910-107_910-95delT others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331469 | ||||||
| chr12:123331519
|
T | C | 1 | a0001c0002t0085g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.910-144A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331519 | ||||||
| chr12:123331582
|
C | T | 214 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.910-207G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331582 | ||||||
| chr12:123331670
|
C | T | 12 | a0002c0004t0020g0039a0002c0004t0020g0078a0002c0004t0020g0091others(9): Show | 12 | HG01358.hp1 HG02280.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-295G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331670 | ||||||
| chr12:123331697
|
A | G | 1 | a0001c0001t0028g0152 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.910-322T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331697 | ||||||
| chr12:123331742
|
G | A | 1 | a0001c0006t0010g0009 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.910-367C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331742 | ||||||
| chr12:123331756
|
G | A | 3 | a0001c0003t0030g0085a0002c0004t0020g0078a0002c0004t0020g0091 | 3 | HG02280.hp1 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.910-381C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331756 | ||||||
| chr12:123331771
|
C | T | 1 | a0003c0007t0041g0019 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.910-396G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331771 | ||||||
| chr12:123331772
|
A | G | 1 | a0003c0007t0041g0019 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.910-397T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331772 | ||||||
| chr12:123331799
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.910-424A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123331799 | ||||||
| chr12:123332015
|
C | A | 2 | a0001c0006t0011g0002a0001c0006t0011g0004 | 2 | HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.910-640G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332015 | ||||||
| chr12:123332138
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.910-763G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332138 | ||||||
| chr12:123332378
|
G | A | 1 | a0001c0003t0069g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.910-1003C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332378 | ||||||
| chr12:123332490
|
C | A | 2 | a0001c0005t0025g0201a0001c0005t0048g0118 | 2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.910-1115G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332490 | ||||||
| chr12:123332534
|
C | T | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.910-1159G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332534 | ||||||
| chr12:123332592
|
A | C | 5 | a0001c0003t0030g0085a0001c0003t0030g0090a0001c0003t0064g0086others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1217T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332592 | ||||||
| chr12:123332715
|
T | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.909+1338A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332715 | ||||||
| chr12:123332779
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.909+1274G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332779 | ||||||
| chr12:123332836
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.909+1217C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332836 | ||||||
| chr12:123332900
|
G | A | 11 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.909+1153C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332900 | ||||||
| chr12:123332930
|
C | A | 2 | a0001c0001t0004g0141a0001c0001t0004g0142 | 2 | HG00280.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.909+1123G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332930 | ||||||
| chr12:123332964
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.909+1089T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332964 | ||||||
| chr12:123332985
|
G | A | 3 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004 | 3 | HG01175.hp2 HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.909+1068C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123332985 | ||||||
| chr12:123333016
|
C | A | 94 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.909+1037G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333016 | ||||||
| chr12:123333022
|
G | T | 28 | a0002c0004t0002g0038a0002c0004t0002g0040a0002c0004t0002g0043others(25): Show | 28 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.909+1031C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333022 | ||||||
| chr12:123333023
|
C | T | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.909+1030G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333023 | ||||||
| chr12:123333029
|
C | G | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.909+1024G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333029 | ||||||
| chr12:123333037
|
T | C | 1 | a0001c0003t0005g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.909+1016A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333037 | ||||||
| chr12:123333099
|
G | A | 6 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+954C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333099 | ||||||
| chr12:123333102
|
C | T | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.909+951G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333102 | ||||||
| chr12:123333123
|
CA | C | 216 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.909+929delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333123 | ||||||
| chr12:123333134
|
A | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.909+919T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333134 | ||||||
| chr12:123333249
|
T | C | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.909+804A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333249 | ||||||
| chr12:123333263
|
A | T | 1 | a0001c0006t0038g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.909+790T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333263 | ||||||
| chr12:123333281
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.909+772C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333281 | ||||||
| chr12:123333291
|
AC | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.909+761delG | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333291 | ||||||
| chr12:123333300
|
C | A | 1 | a0001c0012t0050g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.909+753G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333300 | ||||||
| chr12:123333460
|
C | T | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+593G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333460 | ||||||
| chr12:123333527
|
G | T | 1 | a0001c0001t0083g0124 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.909+526C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333527 | ||||||
| chr12:123333635
|
T | C | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.909+418A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333635 | ||||||
| chr12:123333637
|
C | T | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.909+416G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333637 | ||||||
| chr12:123333643
|
C | T | 4 | a0001c0003t0014g0074a0001c0003t0014g0075a0001c0003t0014g0076others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+410G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333643 | ||||||
| chr12:123333877
|
T | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.909+176A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333877 | ||||||
| chr12:123333927
|
T | C | 2 | a0001c0001t0029g0133a0001c0001t0029g0137 | 2 | NA19003.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.909+126A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 7/31 | chr12 | 123333927 | ||||||
| chr12:123334245
|
A | C | 1 | a0001c0002t0021g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.749-32T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334245 | ||||||
| chr12:123334306
|
CAT | C | 8 | a0001c0006t0010g0007a0001c0006t0010g0011a0001c0006t0010g0013others(5): Show | 8 | HG00280.hp2 HG01943.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.749-95_749-94delAT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334306 | ||||||
| chr12:123334308
|
T | C | 1 | a0001c0002t0003g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.749-95A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334308 | ||||||
| chr12:123334484
|
G | T | 1 | a0002c0004t0079g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.749-271C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334484 | ||||||
| chr12:123334578
|
C | T | 94 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.749-365G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334578 | ||||||
| chr12:123334693
|
G | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0199others(1): Show | 4 | HG02132.hp2 NA18953.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-480C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334693 | ||||||
| chr12:123334710
|
A | T | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.749-497T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334710 | ||||||
| chr12:123334763
|
T | TA | 12 | a0001c0001t0028g0152a0001c0003t0019g0064a0001c0003t0019g0065others(9): Show | 12 | HG01884.hp2 HG01928.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.749-551dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334763 | ||||||
| chr12:123334776
|
T | TA | 70 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.749-564dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123334776 | ||||||
| chr12:123335006
|
T | C | 3 | a0001c0001t0004g0210a0001c0001t0004g0214a0001c0001t0007g0215 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.749-793A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123335006 | ||||||
| chr12:123335063
|
G | C | 2 | a0001c0001t0033g0167a0001c0001t0033g0186 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.749-850C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123335063 | ||||||
| chr12:123335334
|
G | A | 1 | a0001c0005t0012g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.748+1061C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123335334 | ||||||
| chr12:123335465
|
T | A | 1 | a0005c0017t0059g0184 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.748+930A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123335465 | ||||||
| chr12:123335850
|
T | C | 94 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.748+545A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123335850 | ||||||
| chr12:123336044
|
G | A | 1 | a0003c0007t0041g0019 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.748+351C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123336044 | ||||||
| chr12:123336233
|
G | T | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.748+162C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 6/31 | chr12 | 123336233 | ||||||
| chr12:123336510
|
A | G | 3 | a0001c0003t0014g0074a0001c0003t0014g0075a0001c0003t0014g0076 | 3 | HG01891.hp2 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.652-19T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123336510 | ||||||
| chr12:123336607
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.652-116G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123336607 | ||||||
| chr12:123336687
|
T | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.652-196A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123336687 | ||||||
| chr12:123336730
|
G | A | 3 | a0001c0003t0005g0033a0001c0003t0023g0024a0001c0015t0051g0128 | 3 | HG01943.hp1 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.652-239C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123336730 | ||||||
| chr12:123336851
|
A | G | 1 | a0001c0005t0016g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.652-360T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123336851 | ||||||
| chr12:123336864
|
T | G | 1 | a0001c0003t0005g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.652-373A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123336864 | ||||||
| chr12:123337062
|
A | C | 4 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004others(1): Show | 4 | HG01175.hp2 HG02683.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-571T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337062 | ||||||
| chr12:123337245
|
A | G | 1 | a0001c0005t0048g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.652-754T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337245 | ||||||
| chr12:123337411
|
G | A | 1 | a0002c0004t0081g0042 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.652-920C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337411 | ||||||
| chr12:123337795
|
G | A | 1 | a0001c0002t0086g0220 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.652-1304C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337795 | ||||||
| chr12:123337811
|
G | A | 216 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.652-1320C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337811 | ||||||
| chr12:123337852
|
C | A | 14 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(11): Show | 14 | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-1361G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337852 | ||||||
| chr12:123337900
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0173 | 3 | NA18963.hp2 NA18999.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.652-1409A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337900 | ||||||
| chr12:123337905
|
A | G | 1 | a0001c0005t0048g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.652-1414T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337905 | ||||||
| chr12:123337956
|
G | A | 11 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.652-1465C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123337956 | ||||||
| chr12:123338013
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.652-1522T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338013 | ||||||
| chr12:123338092
|
T | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.652-1601A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338092 | ||||||
| chr12:123338118
|
G | A | 1 | a0001c0005t0006g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.652-1627C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338118 | ||||||
| chr12:123338164
|
G | A | 46 | a0001c0003t0014g0074a0001c0003t0014g0075a0001c0003t0014g0076others(43): Show | 46 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.652-1673C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338164 | ||||||
| chr12:123338188
|
C | T | 1 | a0001c0002t0034g0218 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.652-1697G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338188 | ||||||
| chr12:123338313
|
CA | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.652-1823delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338313 | ||||||
| chr12:123338449
|
G | A | 1 | a0001c0015t0051g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.652-1958C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338449 | ||||||
| chr12:123338517
|
T | C | 1 | a0001c0003t0005g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.652-2026A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338517 | ||||||
| chr12:123338532
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.652-2041C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338532 | ||||||
| chr12:123338622
|
T | G | 1 | a0001c0001t0007g0179 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.652-2131A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338622 | ||||||
| chr12:123338819
|
G | A | 1 | a0001c0001t0058g0196 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.651+2169C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338819 | ||||||
| chr12:123338871
|
AACACACA others(15): Show |
A | 161 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.651+2095_651+2116d others(24): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338871 | ||||||
| chr12:123338879
|
CACACACA others(7): Show |
C | 3 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004 | 3 | HG01175.hp2 HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.651+2095_651+2108d others(16): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338879 | ||||||
| chr12:123338881
|
C | T | 31 | a0001c0003t0019g0065a0001c0003t0071g0067a0001c0005t0006g0104others(28): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.651+2107G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338881 | ||||||
| chr12:123338881
|
CACACACA others(5): Show |
C | 10 | a0001c0006t0011g0023a0003c0007t0008g0001a0003c0007t0008g0016others(7): Show | 10 | HG01358.hp1 HG02602.hp1 HG03471.hp2 others(7): Show |
intron_variant | MODIFIER | c.651+2095_651+2106d others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338881 | ||||||
| chr12:123338883
|
CACACACC others(3): Show |
C | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.651+2095_651+2104d others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338883 | ||||||
| chr12:123338887
|
CACCCCG | C | 6 | a0001c0006t0010g0009a0001c0006t0010g0011a0001c0006t0010g0013others(3): Show | 6 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+2095_651+2100d others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338887 | ||||||
| chr12:123338888
|
ACCCCGAC others(17): Show |
A | 25 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.651+2076_651+2099d others(26): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338888 | ||||||
| chr12:123338889
|
CCCCGACA others(16): Show |
C | 4 | a0001c0005t0015g0205a0001c0005t0015g0206a0001c0005t0015g0207others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.651+2076_651+2098d others(25): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338889 | ||||||
| chr12:123338890
|
C | A | 3 | a0001c0006t0010g0007a0001c0006t0037g0006a0001c0006t0038g0010 | 3 | NA18972.hp1 NA19056.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.651+2098G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338890 | ||||||
| chr12:123338890
|
C | G | 2 | a0001c0003t0019g0065a0001c0003t0071g0067 | 2 | HG02055.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.651+2098G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338890 | ||||||
| chr12:123338891
|
CCGACACA others(14): Show |
C | 2 | a0001c0003t0019g0065a0001c0003t0071g0067 | 2 | HG02055.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.651+2076_651+2096d others(23): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338891 | ||||||
| chr12:123338892
|
C | A | 1 | a0001c0006t0010g0007 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.651+2096G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338892 | ||||||
| chr12:123338893
|
G | C | 1 | a0001c0006t0010g0007 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.651+2095C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338893 | ||||||
| chr12:123338903
|
C | T | 161 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.651+2085G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338903 | ||||||
| chr12:123338912
|
GC | G | 16 | a0001c0002t0003g0219a0001c0002t0003g0224a0001c0002t0003g0225others(13): Show | 16 | HG00673.hp1 HG01070.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.651+2075delG | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338912 | ||||||
| chr12:123338913
|
C | G | 4 | a0001c0005t0015g0205a0001c0005t0015g0206a0001c0005t0015g0207others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.651+2075G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338913 | ||||||
| chr12:123338914
|
C | G | 25 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.651+2074G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338914 | ||||||
| chr12:123338916
|
C | G | 22 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(19): Show | 22 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.651+2072G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338916 | ||||||
| chr12:123338922
|
C | A | 146 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.651+2066G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338922 | ||||||
| chr12:123338923
|
C | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0203a0001c0001t0007g0180others(3): Show | 6 | HG02145.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+2065G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338923 | ||||||
| chr12:123338923
|
CCT | C | 159 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(156): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.651+2063_651+2064d others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338923 | ||||||
| chr12:123338924
|
C | A | 40 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(37): Show | 40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.651+2064G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338924 | ||||||
| chr12:123338924
|
CT | C | 13 | a0001c0001t0001g0145a0001c0001t0001g0203a0001c0001t0007g0180others(10): Show | 13 | HG00280.hp2 HG01952.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.651+2063delA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338924 | ||||||
| chr12:123338925
|
T | A | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.651+2063A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338925 | ||||||
| chr12:123338925
|
T | C | 15 | a0001c0002t0009g0242a0001c0003t0019g0064a0001c0003t0019g0065others(12): Show | 15 | HG01175.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.651+2063A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338925 | ||||||
| chr12:123338999
|
A | G | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.651+1989T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123338999 | ||||||
| chr12:123339068
|
T | C | 1 | a0001c0003t0044g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.651+1920A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123339068 | ||||||
| chr12:123339138
|
G | A | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.651+1850C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123339138 | ||||||
| chr12:123339655
|
T | C | 218 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.651+1333A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123339655 | ||||||
| chr12:123339860
|
T | C | 1 | a0001c0005t0006g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.651+1128A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123339860 | ||||||
| chr12:123340052
|
T | TCCAAATT others(32): Show |
1 | a0001c0002t0091g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.651+897_651+935dup others(39): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340052 | ||||||
| chr12:123340088
|
C | T | 42 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(39): Show | 42 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.651+900G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340088 | ||||||
| chr12:123340098
|
G | A | 1 | a0001c0011t0003g0235 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.651+890C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340098 | ||||||
| chr12:123340340
|
G | A | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.651+648C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340340 | ||||||
| chr12:123340363
|
C | T | 2 | a0001c0005t0006g0104a0001c0005t0006g0106 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.651+625G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340363 | ||||||
| chr12:123340367
|
G | C | 4 | a0001c0003t0014g0074a0001c0003t0014g0075a0001c0003t0014g0076others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+621C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340367 | ||||||
| chr12:123340439
|
A | G | 216 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.651+549T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340439 | ||||||
| chr12:123340447
|
G | A | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.651+541C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340447 | ||||||
| chr12:123340581
|
C | CA | 88 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.651+406dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340581 | ||||||
| chr12:123340581
|
C | CAA | 8 | a0001c0003t0043g0035a0001c0006t0011g0002a0001c0006t0011g0003others(5): Show | 8 | HG01175.hp2 HG02109.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.651+405_651+406dup others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340581 | ||||||
| chr12:123340581
|
CA | C | 6 | a0001c0001t0001g0174a0001c0001t0057g0131a0001c0002t0003g0224others(3): Show | 6 | HG01074.hp1 HG02155.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+406delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340581 | ||||||
| chr12:123340604
|
AAG | A | 23 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(20): Show | 23 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.651+382_651+383del others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340604 | ||||||
| chr12:123340605
|
AG | A | 4 | a0001c0005t0012g0110a0001c0005t0012g0114a0001c0005t0012g0117others(1): Show | 4 | HG02109.hp1 HG02257.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+382delC | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340605 | ||||||
| chr12:123340606
|
G | A | 2 | a0001c0005t0006g0109a0001c0005t0016g0098 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.651+382C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340606 | ||||||
| chr12:123340610
|
C | G | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.651+378G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340610 | ||||||
| chr12:123340646
|
A | G | 1 | a0001c0003t0014g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.651+342T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340646 | ||||||
| chr12:123340658
|
C | A | 2 | a0001c0001t0007g0200a0001c0001t0063g0188 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.651+330G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340658 | ||||||
| chr12:123340729
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG02165.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.651+259G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340729 | ||||||
| chr12:123340792
|
A | G | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.651+196T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340792 | ||||||
| chr12:123340842
|
T | C | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.651+146A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340842 | ||||||
| chr12:123340867
|
G | A | 6 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+121C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340867 | ||||||
| chr12:123340947
|
C | G | 1 | a0001c0001t0017g0185 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.651+41G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 5/31 | chr12 | 123340947 | ||||||
| chr12:123341093
|
G | A | 6 | a0001c0001t0001g0120a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG00438.hp1 HG01928.hp1 HG02080.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.551-5C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341093 | ||||||
| chr12:123341460
|
T | C | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.551-372A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341460 | ||||||
| chr12:123341551
|
C | A | 1 | a0001c0003t0030g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.551-463G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341551 | ||||||
| chr12:123341574
|
T | C | 1 | a0001c0001t0004g0143 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.551-486A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341574 | ||||||
| chr12:123341671
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.551-583C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341671 | ||||||
| chr12:123341692
|
T | C | 1 | a0001c0006t0010g0014 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.551-604A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341692 | ||||||
| chr12:123341769
|
C | A | 22 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(19): Show | 22 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.551-681G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341769 | ||||||
| chr12:123341794
|
C | T | 1 | a0001c0005t0025g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.551-706G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341794 | ||||||
| chr12:123341796
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0173 | 2 | NA18963.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.551-708C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123341796 | ||||||
| chr12:123342027
|
G | A | 2 | a0001c0003t0014g0075a0001c0003t0014g0076 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.551-939C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342027 | ||||||
| chr12:123342035
|
G | A | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.551-947C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342035 | ||||||
| chr12:123342095
|
T | C | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.551-1007A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342095 | ||||||
| chr12:123342162
|
A | G | 3 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004 | 3 | HG01175.hp2 HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.551-1074T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342162 | ||||||
| chr12:123342207
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.551-1119T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342207 | ||||||
| chr12:123342227
|
G | A | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.551-1139C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342227 | ||||||
| chr12:123342276
|
A | T | 1 | a0001c0002t0091g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.551-1188T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342276 | ||||||
| chr12:123342383
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.551-1295T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342383 | ||||||
| chr12:123342393
|
A | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.551-1305T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342393 | ||||||
| chr12:123342436
|
T | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.551-1348A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342436 | ||||||
| chr12:123342526
|
T | C | 1 | a0001c0002t0091g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.551-1438A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342526 | ||||||
| chr12:123342559
|
G | A | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.551-1471C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342559 | ||||||
| chr12:123342590
|
C | A | 1 | a0001c0002t0091g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.551-1502G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342590 | ||||||
| chr12:123342755
|
G | GA | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.551-1668dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123342755 | ||||||
| chr12:123343018
|
G | C | 3 | a0001c0010t0060g0130a0001c0010t0061g0119a0001c0013t0070g0193 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.551-1930C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343018 | ||||||
| chr12:123343363
|
G | C | 1 | a0001c0001t0027g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.550+1895C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343363 | ||||||
| chr12:123343460
|
T | C | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.550+1798A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343460 | ||||||
| chr12:123343537
|
C | CT | 25 | a0001c0001t0001g0145a0001c0001t0004g0213a0001c0002t0009g0242others(22): Show | 25 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.550+1720dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343537 | ||||||
| chr12:123343537
|
CT | C | 7 | a0001c0001t0001g0122a0001c0001t0001g0134a0001c0001t0001g0163others(4): Show | 7 | HG02976.hp1 HG03041.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+1720delA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343537 | ||||||
| chr12:123343586
|
T | A | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.550+1672A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343586 | ||||||
| chr12:123343595
|
G | A | 1 | a0001c0006t0038g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.550+1663C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343595 | ||||||
| chr12:123343612
|
G | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.550+1646C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343612 | ||||||
| chr12:123343682
|
T | A | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.550+1576A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123343682 | ||||||
| chr12:123344009
|
C | T | 4 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004others(1): Show | 4 | HG01175.hp2 HG02683.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+1249G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344009 | ||||||
| chr12:123344161
|
G | A | 1 | a0001c0001t0054g0164 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.550+1097C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344161 | ||||||
| chr12:123344245
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.550+1013C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344245 | ||||||
| chr12:123344279
|
T | A | 216 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.550+979A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344279 | ||||||
| chr12:123344385
|
A | G | 1 | a0001c0003t0005g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.550+873T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344385 | ||||||
| chr12:123344481
|
A | G | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.550+777T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344481 | ||||||
| chr12:123344569
|
G | A | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.550+689C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344569 | ||||||
| chr12:123344573
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.550+685T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344573 | ||||||
| chr12:123344880
|
G | A | 1 | a0001c0003t0068g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.550+378C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344880 | ||||||
| chr12:123344941
|
G | T | 1 | a0001c0005t0006g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.550+317C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123344941 | ||||||
| chr12:123345022
|
T | A | 1 | a0001c0002t0091g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.550+236A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123345022 | ||||||
| chr12:123345233
|
T | C | 3 | a0001c0005t0016g0096a0001c0005t0016g0097a0001c0005t0016g0098 | 3 | HG01884.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.550+25A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123345233 | ||||||
| chr12:123345239
|
C | T | 1 | a0001c0002t0085g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.550+19G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 4/31 | chr12 | 123345239 | ||||||
| chr12:123345789
|
C | T | 1 | a0001c0003t0069g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.238-219G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123345789 | ||||||
| chr12:123346009
|
T | C | 1 | a0001c0001t0004g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.238-439A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123346009 | ||||||
| chr12:123346145
|
G | C | 94 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.238-575C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123346145 | ||||||
| chr12:123346392
|
C | T | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.238-822G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123346392 | ||||||
| chr12:123346437
|
G | A | 1 | a0001c0001t0018g0144 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.238-867C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123346437 | ||||||
| chr12:123346532
|
C | T | 1 | a0001c0010t0060g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.238-962G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123346532 | ||||||
| chr12:123346595
|
C | T | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.238-1025G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123346595 | ||||||
| chr12:123346738
|
T | C | 5 | a0001c0005t0016g0096a0001c0005t0016g0097a0001c0005t0016g0098others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-1168A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123346738 | ||||||
| chr12:123346806
|
G | A | 3 | a0001c0005t0016g0096a0001c0005t0016g0097a0001c0005t0016g0098 | 3 | HG01884.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.237+1223C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123346806 | ||||||
| chr12:123347032
|
G | A | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.237+997C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347032 | ||||||
| chr12:123347077
|
C | CA | 95 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0125others(92): Show | 95 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.237+951dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347077 | ||||||
| chr12:123347154
|
G | A | 1 | a0001c0002t0085g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237+875C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347154 | ||||||
| chr12:123347230
|
G | T | 31 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(28): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.237+799C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347230 | ||||||
| chr12:123347375
|
C | T | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.237+654G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347375 | ||||||
| chr12:123347429
|
T | A | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.237+600A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347429 | ||||||
| chr12:123347565
|
G | A | 11 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(8): Show | 11 | HG00438.hp2 HG02132.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.237+464C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347565 | ||||||
| chr12:123347609
|
T | C | 9 | a0001c0002t0003g0231a0001c0002t0003g0232a0001c0002t0003g0233others(6): Show | 9 | NA18941.hp1 NA18942.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.237+420A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347609 | ||||||
| chr12:123347671
|
G | A | 1 | a0001c0002t0085g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237+358C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347671 | ||||||
| chr12:123347816
|
T | C | 7 | a0001c0001t0004g0210a0001c0001t0004g0212a0001c0001t0004g0213others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+213A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347816 | ||||||
| chr12:123347896
|
G | A | 1 | a0001c0001t0027g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.237+133C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 3/31 | chr12 | 123347896 | ||||||
| chr12:123348163
|
TA | T | 216 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.133-31delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348163 | ||||||
| chr12:123348199
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.133-66C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348199 | ||||||
| chr12:123348243
|
G | A | 4 | a0001c0005t0006g0109a0001c0005t0006g0115a0001c0005t0046g0102others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-110C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348243 | ||||||
| chr12:123348307
|
G | T | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.133-174C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348307 | ||||||
| chr12:123348365
|
T | C | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.133-232A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348365 | ||||||
| chr12:123348390
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.133-257C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348390 | ||||||
| chr12:123348865
|
T | C | 2 | a0003c0007t0008g0020a0003c0007t0008g0021 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.133-732A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348865 | ||||||
| chr12:123348974
|
T | C | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.133-841A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348974 | ||||||
| chr12:123348983
|
C | CT | 101 | a0001c0001t0001g0173a0001c0003t0014g0074a0001c0003t0014g0075others(98): Show | 101 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(98): Show |
intron_variant | MODIFIER | c.133-851dupA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348983 | ||||||
| chr12:123348983
|
C | CTT | 23 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(20): Show | 23 | HG00140.hp2 HG01099.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.133-852_133-851dup others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123348983 | ||||||
| chr12:123349015
|
G | C | 1 | a0001c0002t0003g0249 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.133-882C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123349015 | ||||||
| chr12:123349171
|
T | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.133-1038A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123349171 | ||||||
| chr12:123349530
|
TCTATACG others(56): Show |
T | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.132+717_132+779del others(63): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123349530 | ||||||
| chr12:123349702
|
G | A | 1 | a0002c0004t0002g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.132+608C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123349702 | ||||||
| chr12:123349997
|
G | C | 11 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.132+313C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123349997 | ||||||
| chr12:123350282
|
A | C | 1 | a0001c0013t0070g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.132+28T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 2/31 | chr12 | 123350282 | ||||||
| chr12:123350686
|
G | A | 74 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(71): Show | 74 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1-245C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123350686 | ||||||
| chr12:123350841
|
C | T | 1 | a0001c0006t0011g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1-400G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123350841 | ||||||
| chr12:123350860
|
G | GCAGTGGC others(5): Show |
215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-420_1-419insTGTG others(8): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123350860 | ||||||
| chr12:123350877
|
G | A | 1 | a0002c0004t0002g0053 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1-436C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123350877 | ||||||
| chr12:123350927
|
G | T | 1 | a0001c0005t0048g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1-486C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123350927 | ||||||
| chr12:123350974
|
T | A | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1-533A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123350974 | ||||||
| chr12:123351057
|
G | A | 1 | a0001c0003t0076g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1-616C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123351057 | ||||||
| chr12:123351131
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-690T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123351131 | ||||||
| chr12:123351349
|
AT | A | 3 | a0004c0009t0014g0082a0004c0009t0062g0087a0004c0009t0075g0088 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1-909delA | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123351349 | ||||||
| chr12:123351798
|
T | C | 3 | a0004c0009t0014g0082a0004c0009t0062g0087a0004c0009t0075g0088 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1-1357A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123351798 | ||||||
| chr12:123352066
|
GCCATGGA others(7): Show |
G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-1639_1-1626delGT others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352066 | ||||||
| chr12:123352333
|
C | T | 1 | a0001c0012t0050g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1-1892G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352333 | ||||||
| chr12:123352356
|
A | G | 4 | a0001c0002t0009g0241a0001c0002t0009g0242a0001c0002t0088g0239others(1): Show | 4 | NA18981.hp2 NA18991.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-1915T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352356 | ||||||
| chr12:123352456
|
G | A | 3 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004 | 3 | HG01175.hp2 HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1-2015C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352456 | ||||||
| chr12:123352589
|
G | A | 1 | a0001c0003t0005g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1-2148C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352589 | ||||||
| chr12:123352744
|
C | A | 18 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(15): Show | 18 | HG00280.hp2 HG01358.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1-2303G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352744 | ||||||
| chr12:123352828
|
A | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-2387T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352828 | ||||||
| chr12:123352868
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1-2427C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352868 | ||||||
| chr12:123352884
|
G | A | 2 | a0001c0003t0014g0075a0001c0003t0014g0076 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1-2443C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352884 | ||||||
| chr12:123352954
|
T | C | 2 | a0001c0011t0003g0234a0001c0011t0003g0235 | 2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1-2513A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352954 | ||||||
| chr12:123352997
|
C | T | 1 | a0001c0002t0003g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1-2556G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123352997 | ||||||
| chr12:123353010
|
C | T | 1 | a0001c0002t0091g0223 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1-2569G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123353010 | ||||||
| chr12:123353214
|
C | A | 1 | a0001c0003t0065g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1-2773G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123353214 | ||||||
| chr12:123353393
|
TTCCAATG others(826): Show |
T | 1 | a0001c0001t0017g0185 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1-3785_1-2953del | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123353393 | ||||||
| chr12:123353560
|
C | A | 2 | a0002c0004t0002g0054a0002c0004t0082g0041 | 2 | HG01516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1-3119G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123353560 | ||||||
| chr12:123354088
|
G | A | 1 | a0003c0007t0042g0015 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1-3647C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354088 | ||||||
| chr12:123354128
|
T | G | 1 | a0001c0001t0013g0192 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1-3687A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354128 | ||||||
| chr12:123354227
|
A | G | 1 | a0001c0001t0017g0185 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1-3786T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354227 | ||||||
| chr12:123354229
|
G | A | 1 | a0001c0001t0017g0185 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1-3788C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354229 | ||||||
| chr12:123354390
|
T | C | 1 | a0001c0003t0065g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1-3949A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354390 | ||||||
| chr12:123354505
|
C | T | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-4064G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354505 | ||||||
| chr12:123354545
|
C | T | 1 | a0003c0007t0008g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1-4104G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354545 | ||||||
| chr12:123354682
|
T | C | 1 | a0001c0012t0050g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1-4241A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354682 | ||||||
| chr12:123354731
|
C | T | 1 | a0002c0004t0002g0043 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1-4290G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354731 | ||||||
| chr12:123354740
|
G | A | 1 | a0001c0003t0067g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1-4299C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354740 | ||||||
| chr12:123354818
|
T | C | 2 | a0001c0001t0033g0167a0001c0001t0033g0186 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1-4377A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354818 | ||||||
| chr12:123354819
|
G | C | 3 | a0001c0010t0060g0130a0001c0010t0061g0119a0001c0013t0070g0193 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1-4378C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354819 | ||||||
| chr12:123354868
|
CA | C | 258 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(255): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1-4428delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354868 | ||||||
| chr12:123354872
|
A | T | 1 | a0001c0002t0090g0222 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1-4431T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354872 | ||||||
| chr12:123354942
|
C | G | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1-4501G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123354942 | ||||||
| chr12:123355147
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-4706C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123355147 | ||||||
| chr12:123355340
|
AAAAT | A | 93 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(90): Show | 93 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1-4903_1-4900delAT others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123355340 | ||||||
| chr12:123355473
|
G | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-5032C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123355473 | ||||||
| chr12:123355583
|
G | A | 2 | a0001c0002t0021g0250a0001c0002t0021g0254 | 2 | HG00621.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1-5142C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123355583 | ||||||
| chr12:123355749
|
T | G | 1 | a0001c0003t0069g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1-5308A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123355749 | ||||||
| chr12:123355772
|
G | C | 1 | a0001c0002t0003g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1-5331C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123355772 | ||||||
| chr12:123355801
|
C | T | 6 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-5360G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123355801 | ||||||
| chr12:123356041
|
T | C | 18 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(15): Show | 18 | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1-5600A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356041 | ||||||
| chr12:123356298
|
G | A | 1 | a0001c0006t0010g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1-5857C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356298 | ||||||
| chr12:123356311
|
A | T | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-5870T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356311 | ||||||
| chr12:123356319
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-5878C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356319 | ||||||
| chr12:123356447
|
T | G | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1-6006A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356447 | ||||||
| chr12:123356455
|
C | A | 216 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1-6014G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356455 | ||||||
| chr12:123356525
|
C | T | 1 | a0001c0003t0019g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1-6084G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356525 | ||||||
| chr12:123356645
|
T | C | 1 | a0002c0004t0002g0081 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1-6204A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356645 | ||||||
| chr12:123356659
|
T | G | 258 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(255): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1-6218A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356659 | ||||||
| chr12:123356680
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1-6239A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356680 | ||||||
| chr12:123356723
|
C | T | 4 | a0001c0008t0006g0095a0001c0008t0006g0113a0001c0008t0024g0100others(1): Show | 4 | HG02055.hp1 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-6282G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123356723 | ||||||
| chr12:123357068
|
GTGTGCAG others(2): Show |
G | 3 | a0004c0009t0014g0082a0004c0009t0062g0087a0004c0009t0075g0088 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1-6636_1-6628delTA others(7): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357068 | ||||||
| chr12:123357078
|
G | C | 3 | a0004c0009t0014g0082a0004c0009t0062g0087a0004c0009t0075g0088 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1-6637C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357078 | ||||||
| chr12:123357083
|
T | A | 3 | a0004c0009t0014g0082a0004c0009t0062g0087a0004c0009t0075g0088 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1-6642A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357083 | ||||||
| chr12:123357084
|
T | G | 3 | a0004c0009t0014g0082a0004c0009t0062g0087a0004c0009t0075g0088 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1-6643A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357084 | ||||||
| chr12:123357085
|
A | G | 3 | a0004c0009t0014g0082a0004c0009t0062g0087a0004c0009t0075g0088 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1-6644T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357085 | ||||||
| chr12:123357170
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-6729T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357170 | ||||||
| chr12:123357269
|
T | C | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1-6828A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357269 | ||||||
| chr12:123357346
|
A | G | 3 | a0001c0010t0060g0130a0001c0010t0061g0119a0001c0013t0070g0193 | 3 | HG02145.hp1 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1-6905T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357346 | ||||||
| chr12:123357444
|
G | A | 3 | a0001c0006t0010g0013a0001c0006t0010g0014a0001c0006t0035g0012 | 3 | HG00280.hp2 HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1-7003C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357444 | ||||||
| chr12:123357499
|
T | C | 1 | a0001c0001t0017g0185 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1-7058A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357499 | ||||||
| chr12:123357509
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1-7068C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357509 | ||||||
| chr12:123357579
|
A | G | 1 | a0001c0005t0025g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1+7122T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357579 | ||||||
| chr12:123357602
|
ATGGTGGC others(7): Show |
A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+7085_-1+7098del others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357602 | ||||||
| chr12:123357610
|
G | A | 2 | a0001c0002t0034g0217a0001c0002t0034g0218 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-1+7091C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123357610 | ||||||
| chr12:123358099
|
G | A | 1 | a0002c0004t0020g0078 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-1+6602C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358099 | ||||||
| chr12:123358123
|
A | G | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-1+6578T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358123 | ||||||
| chr12:123358350
|
G | A | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1+6351C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358350 | ||||||
| chr12:123358470
|
C | T | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1+6231G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358470 | ||||||
| chr12:123358491
|
T | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+6210A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358491 | ||||||
| chr12:123358605
|
C | T | 1 | a0002c0004t0020g0078 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-1+6096G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358605 | ||||||
| chr12:123358656
|
T | C | 2 | a0001c0001t0033g0167a0001c0001t0033g0186 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-1+6045A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358656 | ||||||
| chr12:123358675
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+6026T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358675 | ||||||
| chr12:123358692
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+6009T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358692 | ||||||
| chr12:123358700
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-1+6001C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358700 | ||||||
| chr12:123358726
|
C | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+5975G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358726 | ||||||
| chr12:123358742
|
C | CAAAAAAA others(4): Show |
2 | a0001c0010t0061g0119a0001c0013t0070g0193 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-1+5948_-1+5958dup others(11): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358742 | ||||||
| chr12:123358742
|
C | CAAAAAAA others(5): Show |
1 | a0001c0010t0060g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-1+5947_-1+5958dup others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358742 | ||||||
| chr12:123358742
|
CAAA | C | 26 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(23): Show | 26 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+5956_-1+5958del others(3): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358742 | ||||||
| chr12:123358742
|
CAAAAAA | C | 21 | a0001c0005t0025g0094a0001c0006t0010g0007a0001c0006t0010g0009others(18): Show | 21 | HG00280.hp2 HG01358.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.-1+5953_-1+5958del others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358742 | ||||||
| chr12:123358755
|
AAAAAAAA others(6): Show |
A | 1 | a0002c0004t0002g0055 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-1+5933_-1+5945del others(13): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358755 | ||||||
| chr12:123358762
|
AAAAAAG | A | 10 | a0001c0001t0001g0120a0001c0001t0001g0171a0001c0001t0004g0210others(7): Show | 10 | HG00140.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+5933_-1+5938del others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358762 | ||||||
| chr12:123358763
|
AAAAAG | A | 140 | a0001c0001t0001g0099a0001c0001t0001g0122a0001c0001t0001g0125others(137): Show | 140 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-1+5933_-1+5937del others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358763 | ||||||
| chr12:123358764
|
AAAAG | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0187a0001c0001t0013g0172others(6): Show | 9 | HG00673.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+5933_-1+5936del others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358764 | ||||||
| chr12:123358832
|
C | T | 9 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(6): Show | 9 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+5869G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358832 | ||||||
| chr12:123358869
|
T | A | 1 | a0001c0005t0012g0111 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1+5832A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358869 | ||||||
| chr12:123358907
|
C | T | 29 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(26): Show | 29 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1+5794G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358907 | ||||||
| chr12:123358958
|
A | T | 1 | a0002c0004t0082g0041 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-1+5743T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123358958 | ||||||
| chr12:123359212
|
A | C | 258 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(255): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-1+5489T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359212 | ||||||
| chr12:123359212
|
A | T | 1 | a0001c0001t0017g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-1+5489T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359212 | ||||||
| chr12:123359380
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0055g0189 | 2 | NA18948.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-1+5321A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359380 | ||||||
| chr12:123359437
|
T | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+5264A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359437 | ||||||
| chr12:123359532
|
G | A | 1 | a0001c0002t0003g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-1+5169C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359532 | ||||||
| chr12:123359541
|
G | T | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-1+5160C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359541 | ||||||
| chr12:123359550
|
G | A | 9 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(6): Show | 9 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+5151C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359550 | ||||||
| chr12:123359554
|
C | CA | 211 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(208): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-1+5146dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359554 | ||||||
| chr12:123359591
|
T | G | 2 | a0001c0003t0043g0035a0001c0003t0044g0034 | 2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-1+5110A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359591 | ||||||
| chr12:123359679
|
T | C | 1 | a0001c0001t0004g0216 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-1+5022A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123359679 | ||||||
| chr12:123360011
|
C | T | 192 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-1+4690G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360011 | ||||||
| chr12:123360146
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-1+4555C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360146 | ||||||
| chr12:123360153
|
G | A | 3 | a0001c0003t0030g0085a0001c0003t0030g0090a0001c0003t0074g0083 | 3 | HG02559.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1+4548C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360153 | ||||||
| chr12:123360222
|
G | A | 1 | a0001c0001t0004g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-1+4479C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360222 | ||||||
| chr12:123360246
|
CA | C | 191 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0125others(188): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-1+4454delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360246 | ||||||
| chr12:123360489
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+4212T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360489 | ||||||
| chr12:123360602
|
G | A | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+4099C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360602 | ||||||
| chr12:123360804
|
C | T | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.-1+3897G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360804 | ||||||
| chr12:123360871
|
G | A | 1 | a0001c0001t0018g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-1+3830C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360871 | ||||||
| chr12:123360878
|
C | A | 4 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004others(1): Show | 4 | HG01175.hp2 HG02683.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+3823G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360878 | ||||||
| chr12:123360988
|
A | G | 1 | a0001c0010t0061g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-1+3713T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123360988 | ||||||
| chr12:123361198
|
C | T | 9 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(6): Show | 9 | HG00280.hp2 HG01943.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+3503G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361198 | ||||||
| chr12:123361238
|
C | T | 2 | a0001c0005t0046g0102a0001c0005t0047g0103 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-1+3463G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361238 | ||||||
| chr12:123361408
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-1+3293G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361408 | ||||||
| chr12:123361440
|
C | T | 1 | a0001c0005t0025g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1+3261G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361440 | ||||||
| chr12:123361498
|
A | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0202 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-1+3203T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361498 | ||||||
| chr12:123361585
|
T | C | 1 | a0001c0012t0050g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1+3116A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361585 | ||||||
| chr12:123361729
|
T | TA | 35 | a0001c0001t0001g0134a0001c0001t0001g0171a0001c0001t0004g0132others(32): Show | 35 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-1+2971dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361729 | ||||||
| chr12:123361729
|
T | TAA | 119 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(116): Show | 119 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-1+2970_-1+2971dup others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361729 | ||||||
| chr12:123361729
|
T | TAAA | 56 | a0001c0001t0007g0200a0001c0003t0005g0025a0001c0003t0005g0026others(53): Show | 56 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-1+2969_-1+2971dup others(3): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361729 | ||||||
| chr12:123361866
|
C | T | 11 | a0001c0003t0019g0064a0001c0003t0019g0065a0001c0003t0019g0080others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1+2835G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361866 | ||||||
| chr12:123361894
|
A | G | 1 | a0001c0005t0025g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-1+2807T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361894 | ||||||
| chr12:123361899
|
G | T | 1 | a0001c0002t0086g0220 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-1+2802C>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361899 | ||||||
| chr12:123361931
|
G | GAGTTTGA others(13): Show |
1 | a0001c0002t0003g0259 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-1+2750_-1+2769dup others(20): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361931 | ||||||
| chr12:123361968
|
G | A | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1+2733C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123361968 | ||||||
| chr12:123362070
|
C | T | 1 | a0001c0005t0048g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1+2631G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362070 | ||||||
| chr12:123362071
|
A | G | 256 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(253): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-1+2630T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362071 | ||||||
| chr12:123362113
|
C | T | 1 | a0001c0002t0086g0220 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-1+2588G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362113 | ||||||
| chr12:123362114
|
T | G | 1 | a0001c0002t0086g0220 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-1+2587A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362114 | ||||||
| chr12:123362143
|
A | T | 1 | a0001c0005t0048g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1+2558T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362143 | ||||||
| chr12:123362157
|
T | C | 259 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(256): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-1+2544A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362157 | ||||||
| chr12:123362199
|
G | A | 2 | a0001c0005t0012g0110a0001c0005t0012g0111 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+2502C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362199 | ||||||
| chr12:123362203
|
G | C | 1 | a0001c0001t0017g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-1+2498C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362203 | ||||||
| chr12:123362265
|
T | C | 91 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-1+2436A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362265 | ||||||
| chr12:123362305
|
G | C | 1 | a0001c0012t0050g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1+2396C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362305 | ||||||
| chr12:123362410
|
T | A | 5 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0259others(2): Show | 5 | NA18747.hp2 NA18953.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+2291A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362410 | ||||||
| chr12:123362435
|
C | CA | 13 | a0001c0002t0003g0219a0001c0002t0003g0246a0001c0002t0003g0248others(10): Show | 13 | HG00621.hp1 HG02071.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+2265dupT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
C | CAA | 5 | a0001c0002t0003g0259a0001c0002t0009g0251a0001c0002t0009g0252others(2): Show | 5 | HG02523.hp2 NA18963.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+2264_-1+2265dup others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAA | C | 9 | a0001c0001t0001g0190a0001c0001t0013g0192a0001c0002t0086g0220others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+2263_-1+2265del others(3): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAA | C | 51 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(48): Show | 51 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-1+2262_-1+2265del others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAAA | C | 110 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1+2261_-1+2265del others(5): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAAAA | C | 16 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0013g0127others(13): Show | 16 | HG01884.hp2 HG01943.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1+2260_-1+2265del others(6): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0022g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-1+2256_-1+2265del others(10): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0006t0040g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1+2255_-1+2265del others(11): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAAAAA others(5): Show |
C | 17 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(14): Show | 17 | HG00280.hp2 HG01358.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1+2254_-1+2265del others(12): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAAAAA others(6): Show |
C | 7 | a0001c0001t0083g0124a0001c0005t0048g0118a0001c0006t0011g0002others(4): Show | 7 | HG01175.hp2 HG02683.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+2253_-1+2265del others(13): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0085g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1+2252_-1+2265del others(14): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362435
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0003t0068g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-1+2248_-1+2265del others(18): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362435 | ||||||
| chr12:123362479
|
G | A | 9 | a0002c0004t0002g0056a0002c0004t0002g0057a0002c0004t0002g0058others(6): Show | 9 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+2222C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362479 | ||||||
| chr12:123362765
|
C | T | 1 | a0001c0003t0074g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-1+1936G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362765 | ||||||
| chr12:123362768
|
CAA | C | 8 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0198others(5): Show | 8 | HG00741.hp2 HG01167.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+1931_-1+1932del others(2): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362768 | ||||||
| chr12:123362768
|
CAAA | C | 146 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0126others(143): Show | 146 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-1+1930_-1+1932del others(3): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362768 | ||||||
| chr12:123362768
|
CAAAA | C | 59 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0004g0121others(56): Show | 59 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.-1+1929_-1+1932del others(4): Show |
SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362768 | ||||||
| chr12:123362924
|
T | A | 1 | a0001c0002t0086g0220 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-1+1777A>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362924 | ||||||
| chr12:123362925
|
TA | T | 27 | a0001c0001t0001g0099a0001c0003t0023g0024a0001c0005t0006g0104others(24): Show | 27 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-1+1775delT | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362925 | ||||||
| chr12:123362926
|
A | T | 1 | a0001c0002t0086g0220 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-1+1775T>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123362926 | ||||||
| chr12:123363074
|
G | C | 23 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(20): Show | 23 | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1+1627C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123363074 | ||||||
| chr12:123363294
|
C | T | 3 | a0001c0006t0011g0002a0001c0006t0011g0003a0001c0006t0011g0004 | 3 | HG01175.hp2 HG02683.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-1+1407G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123363294 | ||||||
| chr12:123363348
|
C | T | 1 | a0001c0002t0003g0219 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-1+1353G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123363348 | ||||||
| chr12:123363373
|
T | G | 5 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0259others(2): Show | 5 | NA18747.hp2 NA18953.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+1328A>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123363373 | ||||||
| chr12:123363467
|
T | C | 1 | a0001c0002t0095g0260 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-1+1234A>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123363467 | ||||||
| chr12:123363862
|
C | T | 1 | a0001c0005t0025g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1+839G>A | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123363862 | ||||||
| chr12:123363908
|
C | A | 23 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(20): Show | 23 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1+793G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123363908 | ||||||
| chr12:123364054
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-1+647C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364054 | ||||||
| chr12:123364063
|
G | A | 1 | a0002c0004t0020g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-1+638C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364063 | ||||||
| chr12:123364096
|
G | A | 1 | a0002c0004t0002g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-1+605C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364096 | ||||||
| chr12:123364204
|
G | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG02165.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-1+497C>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364204 | ||||||
| chr12:123364349
|
G | A | 22 | a0001c0006t0010g0007a0001c0006t0010g0009a0001c0006t0010g0011others(19): Show | 22 | HG00280.hp2 HG01175.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1+352C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364349 | ||||||
| chr12:123364504
|
A | C | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+197T>G | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364504 | ||||||
| chr12:123364522
|
G | A | 3 | a0001c0005t0015g0205a0001c0005t0015g0206a0001c0005t0015g0207 | 3 | HG02451.hp1 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-1+179C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364522 | ||||||
| chr12:123364524
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-1+177G>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364524 | ||||||
| chr12:123364526
|
C | G | 1 | a0001c0001t0027g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+175G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364526 | ||||||
| chr12:123364549
|
C | G | 69 | a0001c0003t0005g0025a0001c0003t0005g0026a0001c0003t0005g0028others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.-1+152G>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364549 | ||||||
| chr12:123364553
|
A | G | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+148T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364553 | ||||||
| chr12:123364556
|
A | G | 218 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.-1+145T>C | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364556 | ||||||
| chr12:123364630
|
C | CGAG | 215 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0122others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+68_-1+70dupCTC | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364630 | ||||||
| chr12:123364665
|
G | A | 7 | a0001c0001t0004g0210a0001c0001t0004g0212a0001c0001t0004g0213others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+36C>T | SBNO1 | ENSG00000139697.14 | transcript | ENST00000602398.3 | protein_coding | 1/31 | chr12 | 123364665 |