Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 25904 |
|---|---|
| ensemblid | ENSG00000182973.20 |
| hgncid | 23817 |
| symbol | CNOT10 |
| name | CCR4-NOT transcription complex subunit 10 |
| refseq_nuc | NM_015442.3 |
| refseq_prot | NP_056257.1 |
| ensembl_nuc | ENST00000328834.10 |
| ensembl_prot | ENSP00000330060.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 32685188 |
| end | 32773875 |
| strand | + |
| ver | v1.2 |
| region | chr3:32685188-32773875 |
| region5000 | chr3:32680188-32778875 |
| regionname0 | CNOT10_chr3_32685188_32773875 |
| regionname5000 | CNOT10_chr3_32680188_32778875 |
| 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 | 1/1 | 744 | 344 | 80 | 69 | 145 | 14 | 34 | 113 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0002 | 0/0 | 744 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0003 | 0/0 | 744 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0004 | 0/0 | 744 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| 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 | 1/1 | 2235 | 343 | 80 | 69 | 144 | 14 | 34 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| c0002 | 0/0 | 2235 | 8 | 6 | 2 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| c0003 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| c0004 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| c0005 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| 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 | 0/1 | 538 | 336 | 71 | 70 | 146 | 14 | 34 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| t0002 | 0/0 | 538 | 12 | 11 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| t0003 | 1/0 | 538 | 4 | 2 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| t0004 | 0/0 | 538 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| t0005 | 0/0 | 538 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| 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 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0329 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| 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 | 1/1 | 2235 | 343 | 80 | 69 | 144 | 14 | 34 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0001c0003 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0002c0002 | 0/0 | 2235 | 8 | 6 | 2 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0003c0005 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0004c0004 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2772 | 325 | 65 | 67 | 144 | 14 | 34 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0001c0001t0002 | 0/0 | 2772 | 12 | 11 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0001c0001t0003 | 1/0 | 2772 | 4 | 2 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0001c0001t0004 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0001c0001t0005 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0001c0003t0001 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0002c0002t0001 | 0/0 | 2772 | 8 | 6 | 2 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0003c0005t0001 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| a0004c0004t0001 | 0/0 | 2772 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | copy fasta | chr3 | 32680188 | 32778875 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0003g0329 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0003c0005t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| a0004c0004t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | GBR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01106 | hp1 | a0004 | c0004 | t0001 | g0346 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0327 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0272 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0352 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0145 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0330 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18969 | hp1 | a0003 | c0005 | t0001 | g0286 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ASW | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0337 | EUR | TSI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | GIH | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | GIH | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | USA | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | USA | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | USA | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0255 | REF | REF | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0329 | REF | REF | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:32727697
|
A | T | 1 | a0002 | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
missense_variant | MODERATE | c.1042A>T | p.Thr348Ser | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/19 | 1315/2772 | 1042/2235 | 348/744 | chr3 | 32727697 | ||
| chr3:32727862
|
A | C | 1 | a0003 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1207A>C | p.Asn403His | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/19 | 1480/2772 | 1207/2235 | 403/744 | chr3 | 32727862 | ||
| chr3:32759484
|
A | T | 1 | a0004 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1622A>T | p.Tyr541Phe | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/19 | 1895/2772 | 1622/2235 | 541/744 | chr3 | 32759484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:32727699
|
G | A | 1 | a0001c0003 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1044G>A | p.Thr348Thr | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/19 | 1317/2772 | 1044/2235 | 348/744 | chr3 | 32727699 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:32685223
|
T | C | 1 | a0001c0001t0004 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-238T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/19 | 238 | chr3 | 32685223 | |||||
| chr3:32773725
|
A | G | 1 | a0001c0001t0002 | 12 | HG00639.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*114A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 19/19 | 114 | chr3 | 32773725 | |||||
| chr3:32773739
|
A | T | 8 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*128A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 19/19 | 128 | chr3 | 32773739 | |||||
| chr3:32773769
|
A | G | 1 | a0001c0001t0005 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*158A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 19/19 | 158 | chr3 | 32773769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:32685594
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.22+112G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32685594 | ||||||
| chr3:32685624
|
C | T | 1 | a0001c0001t0001g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.22+142C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32685624 | ||||||
| chr3:32685654
|
C | T | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.22+172C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32685654 | ||||||
| chr3:32685830
|
A | G | 1 | a0001c0001t0002g0352 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.22+348A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32685830 | ||||||
| chr3:32685939
|
C | CT | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+467dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32685939 | |||||
| chr3:32686073
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+591T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686073 | ||||||
| chr3:32686085
|
A | G | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+603A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686085 | ||||||
| chr3:32686160
|
T | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.22+678T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686160 | ||||||
| chr3:32686304
|
C | G | 1 | a0001c0001t0001g0337 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.22+822C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686304 | ||||||
| chr3:32686319
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.22+837A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686319 | ||||||
| chr3:32686339
|
A | G | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | NA18991.hp2 NA19005.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.22+857A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686339 | ||||||
| chr3:32686399
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+917G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686399 | ||||||
| chr3:32686611
|
G | A | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.22+1129G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686611 | ||||||
| chr3:32686750
|
G | T | 1 | a0001c0001t0001g0333 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.22+1268G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686750 | ||||||
| chr3:32686912
|
A | G | 1 | a0001c0001t0001g0332 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.22+1430A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686912 | ||||||
| chr3:32686979
|
C | CCT | 52 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(49): Show | 52 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.22+1498_22+1499dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32686979 | |||||
| chr3:32687103
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.22+1621A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687103 | ||||||
| chr3:32687152
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.22+1670A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687152 | ||||||
| chr3:32687286
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+1804G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687286 | ||||||
| chr3:32687286
|
G | GC | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0079others(7): Show | 10 | HG01109.hp2 HG01255.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+1810dupC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687286 | |||||
| chr3:32687293
|
G | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.22+1811G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687293 | ||||||
| chr3:32687295
|
T | C | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+1813T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687295 | ||||||
| chr3:32687297
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.22+1815T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687297 | ||||||
| chr3:32687343
|
A | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+1861A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687343 | ||||||
| chr3:32687409
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.22+1927G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687409 | ||||||
| chr3:32687420
|
C | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+1938C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687420 | ||||||
| chr3:32687437
|
C | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.22+1955C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687437 | ||||||
| chr3:32687438
|
G | GGTTTTTT others(5): Show |
54 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(51): Show | 54 | HG00323.hp1 HG00438.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.22+1957_22+1968dup others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687438 | |||||
| chr3:32687439
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+1959_22+1969dup others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | |||||
| chr3:32687439
|
G | GTTTTTTT others(6): Show |
34 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0277others(31): Show | 34 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(13): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | |||||
| chr3:32687439
|
G | GTTTTTTT others(7): Show |
8 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 8 | HG00735.hp1 HG01175.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | |||||
| chr3:32687439
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0316 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.22+1968_22+1969ins others(15): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | |||||
| chr3:32687439
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0317 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.22+1968_22+1969ins others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | |||||
| chr3:32687439
|
G | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.22+1957G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687439 | ||||||
| chr3:32687440
|
T | TTTTTTTT others(4): Show |
28 | a0001c0001t0001g0087a0001c0001t0001g0185a0001c0001t0001g0186others(25): Show | 28 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687440 | |||||
| chr3:32687440
|
T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.22+1970_22+1981dup others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687440 | |||||
| chr3:32687441
|
T | TTTTTTTT others(2): Show |
6 | a0001c0001t0001g0028a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG00673.hp2 HG01255.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+1967_22+1968ins others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687441 | |||||
| chr3:32687441
|
T | TTTTTTTT others(3): Show |
108 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687441 | |||||
| chr3:32687442
|
T | TTTTTTTT others(1): Show |
26 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0032others(23): Show | 26 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.22+1967_22+1968ins others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687442 | |||||
| chr3:32687442
|
T | TTTTTTTT others(2): Show |
12 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(9): Show | 12 | HG00639.hp1 HG02258.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687442 | |||||
| chr3:32687443
|
T | TTTTTTTG | 21 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 21 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.22+1967_22+1968ins others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687443 | |||||
| chr3:32687443
|
T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0088 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.22+1968_22+1969ins others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687443 | |||||
| chr3:32687444
|
T | TTTTTTG | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+1967_22+1968ins others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687444 | |||||
| chr3:32687446
|
T | TTTTTGTT others(6): Show |
1 | a0001c0001t0001g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.22+1968_22+1969ins others(13): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687446 | |||||
| chr3:32687450
|
T | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+1968T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687450 | ||||||
| chr3:32687452
|
G | GTTTTTTT others(6): Show |
3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02273.hp1 NA18974.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.22+1975_22+1987dup others(13): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687452 | |||||
| chr3:32687452
|
G | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.22+1970G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687452 | ||||||
| chr3:32687453
|
T | G | 101 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0079others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.22+1971T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687453 | ||||||
| chr3:32687453
|
T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0318 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.22+1981_22+1982ins others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687453 | |||||
| chr3:32687454
|
T | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0085others(8): Show | 11 | HG01928.hp2 HG02004.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+1972T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687454 | ||||||
| chr3:32687454
|
T | TTTTTTG | 11 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+1977_22+1978ins others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687454 | |||||
| chr3:32687458
|
T | G | 1 | a0001c0001t0001g0334 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.22+1976T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687458 | ||||||
| chr3:32687459
|
T | TTTTGTTT others(5): Show |
22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+1980_22+1981ins others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687459 | |||||
| chr3:32687462
|
T | G | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+1980T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687462 | ||||||
| chr3:32687465
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.22+1983T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687465 | ||||||
| chr3:32687471
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.22+1989A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687471 | ||||||
| chr3:32687486
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.22+2004C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687486 | ||||||
| chr3:32687491
|
A | C | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+2009A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687491 | ||||||
| chr3:32687538
|
G | A | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+2056G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687538 | ||||||
| chr3:32687545
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.22+2063G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687545 | ||||||
| chr3:32687804
|
G | GT | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+2322_22+2323ins others(1): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687804 | ||||||
| chr3:32687805
|
A | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+2323A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687805 | ||||||
| chr3:32687931
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+2449A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687931 | ||||||
| chr3:32687944
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.22+2462C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687944 | ||||||
| chr3:32687962
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.22+2480G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687962 | ||||||
| chr3:32688076
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.22+2594G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688076 | ||||||
| chr3:32688200
|
T | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | NA18947.hp2 NA18950.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+2718T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688200 | ||||||
| chr3:32688287
|
A | T | 1 | a0001c0001t0001g0072 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.22+2805A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688287 | ||||||
| chr3:32688354
|
T | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+2872T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688354 | ||||||
| chr3:32688393
|
G | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0051 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.22+2911G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688393 | ||||||
| chr3:32688400
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+2918A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688400 | ||||||
| chr3:32688467
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.22+2985C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688467 | ||||||
| chr3:32688570
|
C | A | 1 | a0001c0001t0001g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.22+3088C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688570 | ||||||
| chr3:32688616
|
A | G | 119 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.22+3134A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688616 | ||||||
| chr3:32688623
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.22+3141A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688623 | ||||||
| chr3:32688698
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+3216A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688698 | ||||||
| chr3:32688858
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.22+3376T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688858 | ||||||
| chr3:32688872
|
G | A | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+3390G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688872 | ||||||
| chr3:32688927
|
C | T | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.22+3445C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688927 | ||||||
| chr3:32688989
|
G | C | 1 | a0001c0001t0003g0327 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.22+3507G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688989 | ||||||
| chr3:32688994
|
A | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(349): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.22+3512A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688994 | ||||||
| chr3:32689312
|
C | A | 4 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(1): Show | 4 | HG02258.hp1 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+3830C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689312 | ||||||
| chr3:32689318
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.22+3836C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689318 | ||||||
| chr3:32689353
|
C | CA | 9 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0001g0097others(6): Show | 9 | HG01074.hp2 HG01496.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+3886dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32689353 | |||||
| chr3:32689353
|
CA | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 39 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.22+3886delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32689353 | |||||
| chr3:32689745
|
G | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+4263G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689745 | ||||||
| chr3:32689834
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+4352A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689834 | ||||||
| chr3:32689929
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA18946.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.22+4447T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689929 | ||||||
| chr3:32689965
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.22+4483A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689965 | ||||||
| chr3:32689988
|
T | A | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+4506T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689988 | ||||||
| chr3:32690144
|
CTGATTTA others(21): Show |
C | 1 | a0001c0001t0001g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.22+4663_22+4690del others(28): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690144 | ||||||
| chr3:32690184
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.22+4702G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690184 | ||||||
| chr3:32690268
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+4786T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690268 | ||||||
| chr3:32690364
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.22+4882G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690364 | ||||||
| chr3:32690414
|
T | A | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.22+4932T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690414 | ||||||
| chr3:32690527
|
G | T | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+5045G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690527 | ||||||
| chr3:32690539
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+5057T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690539 | ||||||
| chr3:32690551
|
A | AT | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.22+5082dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32690551 | |||||
| chr3:32690577
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.22+5095C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690577 | ||||||
| chr3:32690578
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.22+5096G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690578 | ||||||
| chr3:32690615
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+5133T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690615 | ||||||
| chr3:32690639
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.22+5157C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690639 | ||||||
| chr3:32690664
|
A | C | 7 | a0001c0001t0001g0091a0001c0001t0001g0179a0001c0001t0001g0180others(4): Show | 7 | NA18943.hp2 NA18946.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.22+5182A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690664 | ||||||
| chr3:32690708
|
G | T | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+5226G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690708 | ||||||
| chr3:32690749
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5267A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690749 | ||||||
| chr3:32690751
|
G | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5269G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690751 | ||||||
| chr3:32690754
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5272G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690754 | ||||||
| chr3:32690758
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5276A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690758 | ||||||
| chr3:32690761
|
C | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5279C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690761 | ||||||
| chr3:32690783
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5301A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690783 | ||||||
| chr3:32690807
|
A | G | 3 | a0001c0001t0001g0201a0002c0002t0001g0272a0002c0002t0001g0273 | 3 | HG00735.hp2 HG01081.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.22+5325A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690807 | ||||||
| chr3:32690827
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+5345A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690827 | ||||||
| chr3:32690936
|
C | T | 52 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(49): Show | 52 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.22+5454C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690936 | ||||||
| chr3:32690952
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+5470A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690952 | ||||||
| chr3:32690997
|
C | CT | 254 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.22+5531dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32690997 | |||||
| chr3:32690997
|
C | CTT | 62 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0027others(59): Show | 62 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.22+5530_22+5531dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32690997 | |||||
| chr3:32690997
|
C | CTTTT | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5528_22+5531dup others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32690997 | |||||
| chr3:32691159
|
C | CT | 19 | a0001c0001t0001g0089a0001c0001t0001g0189a0001c0001t0001g0213others(16): Show | 19 | HG00735.hp1 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.22+5697dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32691159 | |||||
| chr3:32691159
|
CT | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.22+5697delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32691159 | |||||
| chr3:32691161
|
T | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+5679T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691161 | ||||||
| chr3:32691162
|
T | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.22+5680T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691162 | ||||||
| chr3:32691168
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5686T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691168 | ||||||
| chr3:32691230
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.22+5748C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691230 | ||||||
| chr3:32691429
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG02970.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.22+5947G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691429 | ||||||
| chr3:32691512
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.22+6030G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691512 | ||||||
| chr3:32691534
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+6052T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691534 | ||||||
| chr3:32691593
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+6111T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691593 | ||||||
| chr3:32691914
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0076 | 2 | NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.22+6432G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691914 | ||||||
| chr3:32691919
|
G | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(6): Show | 9 | NA18955.hp2 NA18960.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+6437G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691919 | ||||||
| chr3:32692014
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.22+6532G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692014 | ||||||
| chr3:32692051
|
C | CA | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.22+6586dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32692051 | |||||
| chr3:32692077
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.22+6595C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692077 | ||||||
| chr3:32692079
|
CG | C | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+6598delG | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692079 | ||||||
| chr3:32692080
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.22+6598G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692080 | ||||||
| chr3:32692109
|
C | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.22+6627C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692109 | ||||||
| chr3:32692163
|
T | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+6681T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692163 | ||||||
| chr3:32692252
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.22+6770A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692252 | ||||||
| chr3:32692429
|
T | C | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+6947T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692429 | ||||||
| chr3:32692880
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+7398G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692880 | ||||||
| chr3:32693142
|
A | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+7660A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693142 | ||||||
| chr3:32693196
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.22+7714A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693196 | ||||||
| chr3:32693200
|
G | T | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.22+7718G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693200 | ||||||
| chr3:32693293
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+7811C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693293 | ||||||
| chr3:32693310
|
G | A | 3 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0322 | 3 | HG02258.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.22+7828G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693310 | ||||||
| chr3:32693312
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+7830A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693312 | ||||||
| chr3:32693466
|
C | T | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.22+7984C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693466 | ||||||
| chr3:32693498
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+8016G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693498 | ||||||
| chr3:32693543
|
C | CT | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 27 | HG01168.hp1 HG01169.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.22+8076dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32693543 | |||||
| chr3:32693690
|
C | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+8208C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693690 | ||||||
| chr3:32693819
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.22+8337G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693819 | ||||||
| chr3:32693822
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+8340G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693822 | ||||||
| chr3:32694138
|
AT | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0027others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.22+8670delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32694138 | |||||
| chr3:32694138
|
ATT | A | 10 | a0001c0001t0001g0046a0001c0001t0001g0225a0001c0001t0001g0237others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.22+8669_22+8670del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32694138 | |||||
| chr3:32694264
|
C | T | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+8782C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694264 | ||||||
| chr3:32694373
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18946.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.22+8891G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694373 | ||||||
| chr3:32694598
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.22+9116T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694598 | ||||||
| chr3:32694635
|
G | T | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+9153G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694635 | ||||||
| chr3:32694678
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-9190T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694678 | ||||||
| chr3:32694734
|
T | G | 105 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(102): Show | 105 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.23-9134T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694734 | ||||||
| chr3:32694754
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.23-9114T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694754 | ||||||
| chr3:32694808
|
C | G | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-9060C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694808 | ||||||
| chr3:32694853
|
A | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-9015A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694853 | ||||||
| chr3:32694887
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.23-8981C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694887 | ||||||
| chr3:32694889
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.23-8979T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694889 | ||||||
| chr3:32694960
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-8908G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694960 | ||||||
| chr3:32695171
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.23-8697A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695171 | ||||||
| chr3:32695267
|
A | G | 1 | a0001c0001t0002g0352 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.23-8601A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695267 | ||||||
| chr3:32695325
|
T | G | 1 | a0001c0001t0001g0348 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.23-8543T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695325 | ||||||
| chr3:32695611
|
A | G | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.23-8257A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695611 | ||||||
| chr3:32695723
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.23-8145A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695723 | ||||||
| chr3:32695761
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | NA18960.hp2 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-8107A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695761 | ||||||
| chr3:32695963
|
AAG | A | 5 | a0001c0001t0001g0339a0002c0002t0001g0214a0002c0002t0001g0229others(2): Show | 5 | HG01081.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-7900_23-7899del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695963 | |||||
| chr3:32695966
|
AGAGTGTG others(3): Show |
A | 2 | a0001c0001t0001g0011a0001c0001t0001g0338 | 2 | HG02132.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.23-7900_23-7891del others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695966 | |||||
| chr3:32695966
|
AGAGTGTG others(5): Show |
A | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(17): Show | 20 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.23-7900_23-7889del others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695966 | |||||
| chr3:32695966
|
AGAGTGTG others(7): Show |
A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-7900_23-7887del others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695966 | |||||
| chr3:32695966
|
AGAGTGTG others(9): Show |
A | 9 | a0001c0001t0001g0340a0001c0001t0001g0345a0001c0001t0001g0347others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.23-7900_23-7885del others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695966 | |||||
| chr3:32695968
|
A | AGT | 41 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0105others(38): Show | 41 | HG00438.hp2 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-7853_23-7852dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
A | AGTGT | 25 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0107others(22): Show | 25 | HG00558.hp1 HG00738.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.23-7855_23-7852dup others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
A | AGTGTGT | 18 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0115others(15): Show | 18 | HG00597.hp2 HG01255.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.23-7857_23-7852dup others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
A | AGTGTGTG others(1): Show |
8 | a0001c0001t0001g0109a0001c0001t0001g0123a0001c0001t0001g0162others(5): Show | 8 | HG02074.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-7859_23-7852dup others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
A | AGTGTGTG others(3): Show |
2 | a0001c0001t0001g0167a0001c0001t0004g0192 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.23-7861_23-7852dup others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0168 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.23-7863_23-7852dup others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
A | T | 3 | a0001c0001t0001g0024a0002c0002t0001g0269a0002c0002t0001g0271 | 3 | HG03471.hp1 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.23-7900A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695968 | ||||||
| chr3:32695968
|
AGT | A | 39 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0092others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.23-7853_23-7852del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
AGTGT | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0084others(30): Show | 33 | HG00408.hp2 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.23-7855_23-7852del others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
AGTGTGT | A | 9 | a0001c0001t0001g0081a0001c0001t0001g0090a0001c0001t0001g0099others(6): Show | 9 | HG00099.hp1 HG01891.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.23-7857_23-7852del others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0323 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.23-7861_23-7852del others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.23-7863_23-7852del others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.23-7865_23-7852del others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
AGTGTGTG others(9): Show |
A | 7 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0066others(4): Show | 7 | HG00408.hp1 HG01433.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-7867_23-7852del others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
AGTGTGTG others(11): Show |
A | 46 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(43): Show | 46 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.23-7869_23-7852del others(18): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32695968
|
AGTGTGTG others(13): Show |
A | 6 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0118others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-7871_23-7852del others(20): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | |||||
| chr3:32696011
|
G | T | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-7857G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696011 | ||||||
| chr3:32696037
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.23-7831C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696037 | ||||||
| chr3:32696068
|
C | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.23-7800C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696068 | ||||||
| chr3:32696144
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-7724T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696144 | ||||||
| chr3:32696212
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-7656A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696212 | ||||||
| chr3:32696213
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-7655G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696213 | ||||||
| chr3:32696311
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.23-7557G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696311 | ||||||
| chr3:32696315
|
C | CA | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(18): Show | 21 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.23-7541dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32696315 | |||||
| chr3:32696325
|
AAAG | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-7528_23-7526del others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32696325 | |||||
| chr3:32696328
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-7540G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696328 | ||||||
| chr3:32696331
|
G | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0338a0001c0001t0001g0339others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.23-7537G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696331 | ||||||
| chr3:32696333
|
A | G | 1 | a0001c0001t0001g0004 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-7535A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696333 | ||||||
| chr3:32696334
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-7534G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696334 | ||||||
| chr3:32696446
|
A | C | 103 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.23-7422A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696446 | ||||||
| chr3:32696498
|
T | G | 1 | a0001c0001t0003g0327 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.23-7370T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696498 | ||||||
| chr3:32696516
|
G | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0293 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.23-7352G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696516 | ||||||
| chr3:32696534
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-7334T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696534 | ||||||
| chr3:32696566
|
G | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.23-7302G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696566 | ||||||
| chr3:32696790
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-7078T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696790 | ||||||
| chr3:32696931
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.23-6937G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696931 | ||||||
| chr3:32697255
|
C | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-6613C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697255 | ||||||
| chr3:32697276
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-6592A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697276 | ||||||
| chr3:32697336
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.23-6532A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697336 | ||||||
| chr3:32697450
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.23-6418T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697450 | ||||||
| chr3:32697450
|
T | G | 102 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(99): Show | 102 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.23-6418T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697450 | ||||||
| chr3:32697534
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.23-6334G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697534 | ||||||
| chr3:32697540
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.23-6328G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697540 | ||||||
| chr3:32697629
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.23-6239C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697629 | ||||||
| chr3:32697645
|
A | G | 135 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(132): Show | 135 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.23-6223A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697645 | ||||||
| chr3:32697660
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.23-6208A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697660 | ||||||
| chr3:32697667
|
G | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-6201G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697667 | ||||||
| chr3:32697691
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.23-6177T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697691 | ||||||
| chr3:32697722
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-6146T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697722 | ||||||
| chr3:32697813
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-6055A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697813 | ||||||
| chr3:32697894
|
A | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-5974A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697894 | ||||||
| chr3:32698489
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.23-5379T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698489 | ||||||
| chr3:32698611
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-5257T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698611 | ||||||
| chr3:32698749
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0282 | 3 | HG00408.hp1 HG02155.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.23-5119A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698749 | ||||||
| chr3:32698768
|
T | C | 1 | a0001c0001t0001g0333 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.23-5100T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698768 | ||||||
| chr3:32698842
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-5026T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698842 | ||||||
| chr3:32698850
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-5018A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698850 | ||||||
| chr3:32699032
|
C | T | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.23-4836C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699032 | ||||||
| chr3:32699133
|
A | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-4735A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699133 | ||||||
| chr3:32699274
|
A | G | 104 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(101): Show | 104 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.23-4594A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699274 | ||||||
| chr3:32699349
|
G | A | 13 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(10): Show | 13 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-4519G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699349 | ||||||
| chr3:32699423
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0282 | 3 | HG00408.hp1 HG02155.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.23-4445T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699423 | ||||||
| chr3:32699535
|
C | T | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-4333C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699535 | ||||||
| chr3:32699721
|
C | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.23-4147C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699721 | ||||||
| chr3:32699975
|
C | CT | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 46 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.23-3875dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32699975 | |||||
| chr3:32699975
|
CT | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0104a0001c0001t0001g0131others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-3875delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32699975 | |||||
| chr3:32700020
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.23-3848G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700020 | ||||||
| chr3:32700041
|
T | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-3827T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700041 | ||||||
| chr3:32700107
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23-3761C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700107 | ||||||
| chr3:32700112
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.23-3756A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700112 | ||||||
| chr3:32700255
|
C | T | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-3613C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700255 | ||||||
| chr3:32700275
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.23-3593C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700275 | ||||||
| chr3:32700639
|
G | A | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.23-3229G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700639 | ||||||
| chr3:32700826
|
A | G | 4 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0215others(1): Show | 4 | HG00639.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-3042A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700826 | ||||||
| chr3:32700962
|
G | T | 1 | a0001c0001t0001g0004 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-2906G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700962 | ||||||
| chr3:32700999
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.23-2869C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700999 | ||||||
| chr3:32701167
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-2701T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701167 | ||||||
| chr3:32701284
|
CTA | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.23-2577_23-2576del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32701284 | |||||
| chr3:32701443
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.23-2425A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701443 | ||||||
| chr3:32701622
|
C | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0292a0001c0001t0001g0300 | 3 | HG00597.hp1 HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.23-2246C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701622 | ||||||
| chr3:32701792
|
G | T | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(349): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.23-2076G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701792 | ||||||
| chr3:32701853
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-2015T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701853 | ||||||
| chr3:32701861
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.23-2007C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701861 | ||||||
| chr3:32701898
|
T | C | 53 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.23-1970T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701898 | ||||||
| chr3:32701932
|
A | G | 1 | a0001c0001t0001g0017 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.23-1936A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701932 | ||||||
| chr3:32702073
|
C | A | 135 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(132): Show | 135 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.23-1795C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702073 | ||||||
| chr3:32702087
|
C | T | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-1781C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702087 | ||||||
| chr3:32702088
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-1780A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702088 | ||||||
| chr3:32702097
|
C | CT | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.23-1756dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702097 | |||||
| chr3:32702097
|
C | CTT | 13 | a0001c0001t0001g0114a0001c0001t0001g0193a0001c0001t0001g0195others(10): Show | 13 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-1757_23-1756dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702097 | |||||
| chr3:32702257
|
A | C | 103 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.23-1611A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702257 | ||||||
| chr3:32702325
|
T | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0110 | 2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.23-1543T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702325 | ||||||
| chr3:32702338
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.23-1530T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702338 | ||||||
| chr3:32702359
|
AT | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(52): Show | 55 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.23-1504delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702359 | |||||
| chr3:32702514
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.23-1354A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702514 | ||||||
| chr3:32702530
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-1338T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702530 | ||||||
| chr3:32702606
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.23-1262A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702606 | ||||||
| chr3:32702664
|
G | A | 2 | a0001c0001t0001g0178a0001c0003t0001g0145 | 2 | HG02083.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.23-1204G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702664 | ||||||
| chr3:32702916
|
G | GT | 6 | a0001c0001t0001g0125a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | NA18945.hp1 NA18955.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-939dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702916 | |||||
| chr3:32702916
|
GT | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.23-939delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702916 | |||||
| chr3:32702976
|
A | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-892A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702976 | ||||||
| chr3:32702985
|
C | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-883C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702985 | ||||||
| chr3:32703013
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.23-855G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703013 | ||||||
| chr3:32703078
|
A | AT | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.23-771dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32703078 | |||||
| chr3:32703078
|
A | ATT | 25 | a0001c0001t0001g0064a0001c0001t0001g0083a0001c0001t0001g0097others(22): Show | 25 | HG00140.hp2 HG00735.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.23-772_23-771dupTT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32703078 | |||||
| chr3:32703096
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0339 | 2 | HG01255.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.23-772T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703096 | ||||||
| chr3:32703104
|
T | C | 29 | a0001c0001t0001g0081a0001c0001t0001g0126a0001c0001t0001g0199others(26): Show | 29 | HG00639.hp1 HG01081.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.23-764T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703104 | ||||||
| chr3:32703147
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(58): Show | 61 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.23-721A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703147 | ||||||
| chr3:32703203
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.23-665C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703203 | ||||||
| chr3:32703213
|
C | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(17): Show | 20 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.23-655C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703213 | ||||||
| chr3:32703215
|
T | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.23-653T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703215 | ||||||
| chr3:32703219
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | NA18960.hp2 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-649T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703219 | ||||||
| chr3:32703466
|
C | T | 103 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(100): Show | 103 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.23-402C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703466 | ||||||
| chr3:32703579
|
A | G | 1 | a0003c0005t0001g0286 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.23-289A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703579 | ||||||
| chr3:32703623
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.23-245A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703623 | ||||||
| chr3:32703983
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.117+21G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32703983 | ||||||
| chr3:32704121
|
T | G | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.117+159T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704121 | ||||||
| chr3:32704140
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0053a0001c0001t0001g0058others(1): Show | 4 | HG00438.hp1 NA19007.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+178A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704140 | ||||||
| chr3:32704304
|
T | G | 103 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.117+342T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704304 | ||||||
| chr3:32704470
|
T | C | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-341T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704470 | ||||||
| chr3:32704545
|
A | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-266A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704545 | ||||||
| chr3:32704796
|
G | GT | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
splice_acceptor_variant&intron_variant | HIGH | c.118-3dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 32704796 | |||||
| chr3:32705030
|
A | G | 112 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(109): Show | 112 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.279+58A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705030 | ||||||
| chr3:32705164
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | NA18612.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.279+192T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705164 | ||||||
| chr3:32705267
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0242 | 2 | HG02080.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.279+295A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705267 | ||||||
| chr3:32705485
|
G | C | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.279+513G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705485 | ||||||
| chr3:32705566
|
T | C | 1 | a0001c0001t0001g0290 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.279+594T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705566 | ||||||
| chr3:32705709
|
A | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+737A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705709 | ||||||
| chr3:32705762
|
C | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | NA18960.hp2 NA18962.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+790C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705762 | ||||||
| chr3:32705783
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(51): Show | 54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.279+811T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705783 | ||||||
| chr3:32706152
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.279+1180G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706152 | ||||||
| chr3:32706248
|
A | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.279+1276A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706248 | ||||||
| chr3:32706546
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.279+1574T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706546 | ||||||
| chr3:32706628
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.279+1656A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706628 | ||||||
| chr3:32706803
|
C | G | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.279+1831C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706803 | ||||||
| chr3:32706925
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.280-1745T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706925 | ||||||
| chr3:32707100
|
A | G | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.280-1570A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707100 | ||||||
| chr3:32707275
|
CT | C | 6 | a0001c0001t0001g0224a0001c0001t0001g0239a0001c0001t0001g0242others(3): Show | 6 | HG00408.hp2 HG02080.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-1383delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr3 | 32707275 | |||||
| chr3:32707308
|
G | A | 2 | a0001c0001t0001g0178a0001c0003t0001g0145 | 2 | HG02083.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.280-1362G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707308 | ||||||
| chr3:32707422
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.280-1248G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707422 | ||||||
| chr3:32707570
|
G | A | 1 | a0001c0001t0003g0330 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280-1100G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707570 | ||||||
| chr3:32707583
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.280-1087C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707583 | ||||||
| chr3:32707812
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.280-858A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707812 | ||||||
| chr3:32708031
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.280-639A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708031 | ||||||
| chr3:32708037
|
G | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.280-633G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708037 | ||||||
| chr3:32708194
|
G | A | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.280-476G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708194 | ||||||
| chr3:32708275
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280-395T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708275 | ||||||
| chr3:32708289
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.280-381T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708289 | ||||||
| chr3:32708451
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.280-219T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708451 | ||||||
| chr3:32708489
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.280-181A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708489 | ||||||
| chr3:32708839
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.430+19C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32708839 | ||||||
| chr3:32708861
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.430+41A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32708861 | ||||||
| chr3:32709010
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430+190A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709010 | ||||||
| chr3:32709058
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.430+238T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709058 | ||||||
| chr3:32709113
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+293C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709113 | ||||||
| chr3:32709138
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.430+318A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709138 | ||||||
| chr3:32709229
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430+409G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709229 | ||||||
| chr3:32709317
|
G | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430+497G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709317 | ||||||
| chr3:32709548
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.430+728T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709548 | ||||||
| chr3:32709588
|
G | C | 1 | a0001c0001t0001g0282 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.430+768G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709588 | ||||||
| chr3:32709620
|
C | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+800C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709620 | ||||||
| chr3:32709697
|
AGT | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+879_430+880del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32709697 | |||||
| chr3:32709738
|
A | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+918A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709738 | ||||||
| chr3:32709865
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.430+1045T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709865 | ||||||
| chr3:32710079
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0066others(1): Show | 4 | NA18981.hp2 NA18989.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1259C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710079 | ||||||
| chr3:32710086
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.430+1266G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710086 | ||||||
| chr3:32710147
|
CA | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.430+1349delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32710147 | |||||
| chr3:32710147
|
CAA | C | 13 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0140others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+1348_430+1349d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32710147 | |||||
| chr3:32710147
|
CAAA | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.430+1347_430+1349d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32710147 | |||||
| chr3:32710147
|
CAAAA | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0338a0001c0001t0001g0341others(3): Show | 6 | HG01891.hp1 HG02132.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+1346_430+1349d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32710147 | |||||
| chr3:32710159
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.430+1339A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710159 | ||||||
| chr3:32710236
|
A | T | 1 | a0001c0001t0002g0322 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430+1416A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710236 | ||||||
| chr3:32710289
|
A | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+1469A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710289 | ||||||
| chr3:32710305
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.430+1485G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710305 | ||||||
| chr3:32710322
|
G | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0326 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.430+1502G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710322 | ||||||
| chr3:32710421
|
C | T | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+1601C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710421 | ||||||
| chr3:32710652
|
T | C | 102 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(99): Show | 102 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.430+1832T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710652 | ||||||
| chr3:32710688
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.430+1868G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710688 | ||||||
| chr3:32710779
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.430+1959G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710779 | ||||||
| chr3:32710780
|
G | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.430+1960G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710780 | ||||||
| chr3:32710870
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.430+2050G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710870 | ||||||
| chr3:32711277
|
G | A | 5 | a0001c0001t0001g0338a0001c0001t0001g0341a0001c0001t0001g0342others(2): Show | 5 | HG01891.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-1950G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711277 | ||||||
| chr3:32711617
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-1610T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711617 | ||||||
| chr3:32711704
|
G | C | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-1523G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711704 | ||||||
| chr3:32711862
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0060 | 2 | NA18985.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.431-1365G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711862 | ||||||
| chr3:32711881
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.431-1346T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711881 | ||||||
| chr3:32711934
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.431-1293A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711934 | ||||||
| chr3:32712032
|
CA | C | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.431-1194delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712032 | ||||||
| chr3:32712133
|
G | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.431-1094G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712133 | ||||||
| chr3:32712134
|
C | G | 97 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(94): Show | 97 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.431-1093C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712134 | ||||||
| chr3:32712163
|
G | GT | 172 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.431-1050dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32712163 | |||||
| chr3:32712163
|
G | GTT | 15 | a0001c0001t0001g0033a0001c0001t0001g0063a0001c0001t0001g0066others(12): Show | 15 | HG00597.hp2 HG00673.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.431-1051_431-1050d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32712163 | |||||
| chr3:32712163
|
G | T | 3 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0216 | 3 | HG00639.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.431-1064G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712163 | ||||||
| chr3:32712163
|
GTT | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.431-1051_431-1050d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32712163 | |||||
| chr3:32712167
|
T | G | 1 | a0001c0001t0001g0283 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.431-1060T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712167 | ||||||
| chr3:32712169
|
T | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.431-1058T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712169 | ||||||
| chr3:32712201
|
A | C | 1 | a0002c0002t0001g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431-1026A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712201 | ||||||
| chr3:32712379
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.431-848G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712379 | ||||||
| chr3:32712399
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.431-828T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712399 | ||||||
| chr3:32712424
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0326 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.431-803T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712424 | ||||||
| chr3:32712524
|
T | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-703T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712524 | ||||||
| chr3:32712550
|
A | G | 1 | a0001c0001t0001g0347 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.431-677A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712550 | ||||||
| chr3:32712618
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.431-609G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712618 | ||||||
| chr3:32712846
|
A | G | 1 | a0002c0002t0001g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.431-381A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712846 | ||||||
| chr3:32712866
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.431-361A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712866 | ||||||
| chr3:32712995
|
G | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0274others(1): Show | 4 | NA18954.hp2 NA18963.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-232G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712995 | ||||||
| chr3:32713052
|
G | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-175G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32713052 | ||||||
| chr3:32713124
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-103T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32713124 | ||||||
| chr3:32713162
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.431-65G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32713162 | ||||||
| chr3:32713165
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.431-62G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32713165 | ||||||
| chr3:32713744
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.573+375A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32713744 | ||||||
| chr3:32713824
|
A | AT | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.573+460dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32713824 | |||||
| chr3:32713830
|
G | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+461G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32713830 | ||||||
| chr3:32713897
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.573+528T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32713897 | ||||||
| chr3:32713958
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.573+589A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32713958 | ||||||
| chr3:32714044
|
C | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.573+675C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714044 | ||||||
| chr3:32714083
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.573+714A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714083 | ||||||
| chr3:32714237
|
C | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.573+868C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714237 | ||||||
| chr3:32714405
|
C | CA | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.573+1052dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32714405 | |||||
| chr3:32714405
|
CA | C | 10 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0062others(7): Show | 10 | HG01257.hp2 HG02155.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.573+1052delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32714405 | |||||
| chr3:32714461
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.573+1092C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714461 | ||||||
| chr3:32714535
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.573+1166C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714535 | ||||||
| chr3:32714554
|
C | CA | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.573+1191dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32714554 | |||||
| chr3:32714616
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.573+1247C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714616 | ||||||
| chr3:32714641
|
G | A | 5 | a0001c0001t0001g0235a0001c0001t0001g0249a0001c0001t0001g0293others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1272G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714641 | ||||||
| chr3:32714643
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.573+1274A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714643 | ||||||
| chr3:32714656
|
C | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.573+1287C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714656 | ||||||
| chr3:32714665
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.573+1296C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714665 | ||||||
| chr3:32714666
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0326 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.573+1297G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714666 | ||||||
| chr3:32714718
|
A | C | 1 | a0001c0001t0001g0299 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.573+1349A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714718 | ||||||
| chr3:32714895
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.574-1330C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714895 | ||||||
| chr3:32714926
|
C | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-1299C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714926 | ||||||
| chr3:32715291
|
G | A | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-934G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715291 | ||||||
| chr3:32715485
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.574-740A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715485 | ||||||
| chr3:32715546
|
A | T | 1 | a0001c0001t0002g0325 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.574-679A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715546 | ||||||
| chr3:32715572
|
G | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.574-653G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715572 | ||||||
| chr3:32715655
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.574-570C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715655 | ||||||
| chr3:32715856
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-369A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715856 | ||||||
| chr3:32715951
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.574-274A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715951 | ||||||
| chr3:32715954
|
TG | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-269delG | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32715954 | |||||
| chr3:32716049
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-176C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32716049 | ||||||
| chr3:32716345
|
CAT | C | 4 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+39_660+40delAT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 32716345 | |||||
| chr3:32716370
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.660+59A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716370 | ||||||
| chr3:32716405
|
A | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.660+94A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716405 | ||||||
| chr3:32716418
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.660+107C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716418 | ||||||
| chr3:32716674
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.660+363G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716674 | ||||||
| chr3:32716703
|
A | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0307 | 2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.660+392A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716703 | ||||||
| chr3:32716739
|
C | A | 1 | a0001c0001t0001g0347 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.661-415C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716739 | ||||||
| chr3:32716764
|
C | T | 97 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(94): Show | 97 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.661-390C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716764 | ||||||
| chr3:32716806
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.661-348A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716806 | ||||||
| chr3:32716886
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.661-268G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716886 | ||||||
| chr3:32716899
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.661-255C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716899 | ||||||
| chr3:32716965
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.661-189G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716965 | ||||||
| chr3:32716991
|
C | T | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.661-163C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716991 | ||||||
| chr3:32717269
|
TTG | T | 33 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(30): Show | 33 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.744+36_744+37delGT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32717269 | |||||
| chr3:32717271
|
G | A | 110 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(107): Show | 110 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.744+34G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717271 | ||||||
| chr3:32717403
|
A | AT | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.744+179dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32717403 | |||||
| chr3:32717460
|
A | T | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.744+223A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717460 | ||||||
| chr3:32717470
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.744+233T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717470 | ||||||
| chr3:32717514
|
CACTT | C | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+279_744+282del others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32717514 | |||||
| chr3:32717659
|
A | C | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+422A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717659 | ||||||
| chr3:32717660
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.744+423G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717660 | ||||||
| chr3:32717723
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.744+486G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717723 | ||||||
| chr3:32717891
|
T | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.744+654T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717891 | ||||||
| chr3:32718258
|
C | CT | 18 | a0001c0001t0001g0085a0001c0001t0001g0154a0001c0001t0001g0185others(15): Show | 18 | HG01071.hp2 HG01106.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.744+1043dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718258 | |||||
| chr3:32718258
|
CT | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(32): Show | 35 | HG00099.hp1 HG01099.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.744+1043delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718258 | |||||
| chr3:32718301
|
C | G | 9 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.744+1064C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718301 | ||||||
| chr3:32718435
|
T | C | 2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.744+1198T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718435 | ||||||
| chr3:32718440
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.744+1203C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718440 | ||||||
| chr3:32718444
|
C | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.744+1207C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718444 | ||||||
| chr3:32718509
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.744+1272G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718509 | ||||||
| chr3:32718515
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.744+1278C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718515 | ||||||
| chr3:32718539
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.744+1302G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718539 | ||||||
| chr3:32718583
|
C | CA | 184 | a0001c0001t0001g0055a0001c0001t0001g0079a0001c0001t0001g0082others(181): Show | 184 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.744+1367dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718583 | |||||
| chr3:32718583
|
C | CAA | 19 | a0001c0001t0001g0080a0001c0001t0001g0091a0001c0001t0001g0095others(16): Show | 19 | HG00735.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.744+1366_744+1367d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718583 | |||||
| chr3:32718583
|
CA | C | 18 | a0001c0001t0001g0054a0001c0001t0001g0338a0001c0001t0001g0339others(15): Show | 18 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.744+1367delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718583 | |||||
| chr3:32718833
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.745-1281G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718833 | ||||||
| chr3:32718904
|
C | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.745-1210C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718904 | ||||||
| chr3:32719204
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.745-910G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719204 | ||||||
| chr3:32719228
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.745-886A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719228 | ||||||
| chr3:32719244
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.745-870G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719244 | ||||||
| chr3:32719414
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.745-700C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719414 | ||||||
| chr3:32719429
|
A | C | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.745-685A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719429 | ||||||
| chr3:32719605
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.745-509A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719605 | ||||||
| chr3:32719642
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 91 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.745-472T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719642 | ||||||
| chr3:32719945
|
A | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.745-169A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719945 | ||||||
| chr3:32719989
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.745-125A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719989 | ||||||
| chr3:32719990
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00408.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.745-124T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719990 | ||||||
| chr3:32720101
|
A | G | 1 | a0002c0002t0001g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.745-13A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32720101 | ||||||
| chr3:32720257
|
CT | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.862+34delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720257 | |||||
| chr3:32720379
|
A | G | 5 | a0001c0001t0001g0338a0001c0001t0001g0341a0001c0001t0001g0342others(2): Show | 5 | HG01891.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.862+148A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720379 | ||||||
| chr3:32720512
|
A | AT | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(33): Show | 36 | HG01071.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.862+285dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720512 | |||||
| chr3:32720517
|
A | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.862+286A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720517 | ||||||
| chr3:32720550
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.862+319T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720550 | ||||||
| chr3:32720683
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.862+452T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720683 | ||||||
| chr3:32720727
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.862+496C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720727 | ||||||
| chr3:32720789
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.862+558T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720789 | ||||||
| chr3:32720803
|
T | C | 1 | a0001c0001t0001g0345 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.862+572T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720803 | ||||||
| chr3:32720822
|
G | GCCCTCCC others(1): Show |
15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+600_862+607dup others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720822 | |||||
| chr3:32720831
|
C | CCCTCCCT others(1): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0076 | 3 | NA18981.hp2 NA18989.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.862+627_862+634dup others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720831 | |||||
| chr3:32720843
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.862+612C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720843 | ||||||
| chr3:32720859
|
C | CCCTTCCT others(9): Show |
2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.862+634_862+635ins others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720859 | |||||
| chr3:32720859
|
C | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+628C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720859 | ||||||
| chr3:32720866
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.862+635C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720866 | ||||||
| chr3:32720867
|
T | C | 98 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.862+636T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720867 | ||||||
| chr3:32720874
|
T | C | 98 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.862+643T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720874 | ||||||
| chr3:32720877
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.862+646T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720877 | ||||||
| chr3:32720879
|
T | TCCCTC | 12 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(9): Show | 12 | HG02015.hp2 HG02132.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.862+649_862+650ins others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720879 | |||||
| chr3:32720880
|
C | CCCT | 8 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+649_862+650ins others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720880 | ||||||
| chr3:32720880
|
CT | C | 98 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.862+653delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720880 | |||||
| chr3:32720881
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+650T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720881 | ||||||
| chr3:32720882
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 106 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.862+651T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720882 | ||||||
| chr3:32720882
|
T | TCC | 12 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(9): Show | 12 | HG02015.hp2 HG02132.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.862+651_862+652ins others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720882 | ||||||
| chr3:32720886
|
C | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.862+655C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720886 | ||||||
| chr3:32720891
|
T | TTTCC | 22 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0082others(19): Show | 22 | HG01168.hp2 HG02083.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.862+701_862+704dup others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | |||||
| chr3:32720891
|
T | TTTCCTTC others(5): Show |
2 | a0001c0001t0001g0231a0001c0001t0002g0352 | 2 | HG01891.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.862+693_862+704dup others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | |||||
| chr3:32720891
|
TTTCC | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(27): Show | 30 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.862+701_862+704del others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | |||||
| chr3:32720891
|
TTTCCTTC others(1): Show |
T | 11 | a0001c0001t0001g0001a0001c0001t0001g0102a0001c0001t0001g0103others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.862+697_862+704del others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | |||||
| chr3:32720891
|
TTTCCTTC others(5): Show |
T | 17 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0098others(14): Show | 17 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.862+693_862+704del others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | |||||
| chr3:32720891
|
TTTCCTTC others(9): Show |
T | 3 | a0001c0001t0001g0339a0001c0001t0002g0209a0001c0001t0002g0322 | 3 | HG06807.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.862+689_862+704del others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | |||||
| chr3:32720891
|
TTTCCTTC others(13): Show |
T | 1 | a0001c0001t0001g0334 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.862+685_862+704del others(20): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | |||||
| chr3:32720893
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+662T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720893 | ||||||
| chr3:32720894
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+663C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720894 | ||||||
| chr3:32720895
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+664C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720895 | ||||||
| chr3:32720898
|
C | CT | 15 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(12): Show | 15 | HG00558.hp1 HG02015.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.862+667_862+668ins others(1): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720898 | ||||||
| chr3:32720899
|
C | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.862+668C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720899 | ||||||
| chr3:32720900
|
TTCC | T | 93 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(90): Show | 93 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.862+671_862+673del others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720900 | |||||
| chr3:32720900
|
TTCCTTCC others(4): Show |
T | 1 | a0001c0001t0001g0140 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.862+671_862+681del others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720900 | |||||
| chr3:32720902
|
C | CT | 8 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+671_862+672ins others(1): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720902 | ||||||
| chr3:32720903
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+672C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720903 | ||||||
| chr3:32720949
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.862+718T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720949 | ||||||
| chr3:32721003
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.862+772G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721003 | ||||||
| chr3:32721060
|
C | CGTT | 12 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(9): Show | 12 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.862+829_862+830ins others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721060 | ||||||
| chr3:32721060
|
C | CT | 111 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0088others(108): Show | 111 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.862+848dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721060 | |||||
| chr3:32721060
|
C | CTT | 18 | a0001c0001t0001g0082a0001c0001t0001g0193a0001c0001t0001g0204others(15): Show | 18 | HG00323.hp1 HG00741.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.862+847_862+848dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721060 | |||||
| chr3:32721060
|
CT | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.862+848delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721060 | |||||
| chr3:32721060
|
CTT | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0339others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+847_862+848del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721060 | |||||
| chr3:32721064
|
T | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0110 | 3 | HG00140.hp1 HG01175.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.862+833T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721064 | ||||||
| chr3:32721091
|
G | T | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.862+860G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721091 | ||||||
| chr3:32721133
|
C | T | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+902C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721133 | ||||||
| chr3:32721210
|
C | T | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.862+979C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721210 | ||||||
| chr3:32721351
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00408.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.862+1120C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721351 | ||||||
| chr3:32721390
|
AC | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.862+1160delC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721390 | ||||||
| chr3:32721394
|
T | C | 1 | a0001c0001t0003g0330 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.862+1163T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721394 | ||||||
| chr3:32721422
|
CTTTCATC others(18): Show |
C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.862+1195_862+1219d others(27): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721422 | |||||
| chr3:32721429
|
C | CT | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.862+1223dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721429 | |||||
| chr3:32721429
|
C | CTT | 36 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0065others(33): Show | 36 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.862+1222_862+1223d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721429 | |||||
| chr3:32721429
|
CT | C | 7 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(4): Show | 7 | HG01891.hp1 HG03130.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.862+1223delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721429 | |||||
| chr3:32721429
|
CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+1212_862+1223d others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721429 | |||||
| chr3:32721536
|
T | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+1305T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721536 | ||||||
| chr3:32721647
|
C | CT | 8 | a0001c0001t0001g0064a0001c0001t0001g0070a0001c0001t0001g0115others(5): Show | 8 | HG00140.hp2 HG01109.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+1433dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721647 | |||||
| chr3:32721763
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.862+1532C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721763 | ||||||
| chr3:32721771
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.862+1540C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721771 | ||||||
| chr3:32721898
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.862+1667C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721898 | ||||||
| chr3:32721959
|
T | TA | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.862+1729dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721959 | |||||
| chr3:32721994
|
A | G | 96 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(93): Show | 96 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.862+1763A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721994 | ||||||
| chr3:32722096
|
C | G | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.862+1865C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722096 | ||||||
| chr3:32722204
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.862+1973C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722204 | ||||||
| chr3:32722278
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0326 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.862+2047G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722278 | ||||||
| chr3:32722390
|
A | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.862+2159A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722390 | ||||||
| chr3:32722458
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.862+2227C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722458 | ||||||
| chr3:32722668
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.862+2437G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722668 | ||||||
| chr3:32722740
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.862+2509T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722740 | ||||||
| chr3:32722756
|
G | A | 5 | a0001c0001t0001g0237a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 5 | HG01099.hp1 HG01168.hp2 NA20752.hp2 others(2): Show |
intron_variant | MODIFIER | c.862+2525G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722756 | ||||||
| chr3:32723078
|
T | G | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.863-2372T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723078 | ||||||
| chr3:32723132
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-2318A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723132 | ||||||
| chr3:32723210
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.863-2240G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723210 | ||||||
| chr3:32723220
|
C | T | 98 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.863-2230C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723220 | ||||||
| chr3:32723387
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-2063G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723387 | ||||||
| chr3:32723625
|
AT | A | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.863-1821delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32723625 | |||||
| chr3:32723743
|
G | A | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.863-1707G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723743 | ||||||
| chr3:32723924
|
T | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-1526T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723924 | ||||||
| chr3:32723929
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.863-1521A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723929 | ||||||
| chr3:32724089
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.863-1361A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724089 | ||||||
| chr3:32724135
|
A | G | 97 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(94): Show | 97 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.863-1315A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724135 | ||||||
| chr3:32724171
|
A | G | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.863-1279A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724171 | ||||||
| chr3:32724213
|
A | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.863-1237A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724213 | ||||||
| chr3:32724231
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.863-1219T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724231 | ||||||
| chr3:32724239
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-1211G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724239 | ||||||
| chr3:32724243
|
C | CT | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.863-1189dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32724243 | |||||
| chr3:32724243
|
C | CTT | 8 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0067others(5): Show | 8 | HG01981.hp1 HG02559.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.863-1190_863-1189d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32724243 | |||||
| chr3:32724314
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.863-1136C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724314 | ||||||
| chr3:32724326
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.863-1124A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724326 | ||||||
| chr3:32724328
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.863-1122C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724328 | ||||||
| chr3:32724412
|
A | AT | 29 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0118others(26): Show | 29 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.863-1020dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32724412 | |||||
| chr3:32724436
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.863-1014G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724436 | ||||||
| chr3:32724514
|
G | A | 14 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.863-936G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724514 | ||||||
| chr3:32724574
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-876G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724574 | ||||||
| chr3:32724687
|
C | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-763C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724687 | ||||||
| chr3:32724797
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-653G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724797 | ||||||
| chr3:32724805
|
C | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-645C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724805 | ||||||
| chr3:32724839
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-611A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724839 | ||||||
| chr3:32724844
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.863-606C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724844 | ||||||
| chr3:32724848
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | NA18612.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.863-602C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724848 | ||||||
| chr3:32724869
|
CT | C | 114 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.863-577delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32724869 | |||||
| chr3:32725140
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.863-310G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725140 | ||||||
| chr3:32725150
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.863-300A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725150 | ||||||
| chr3:32725283
|
T | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863-167T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725283 | ||||||
| chr3:32725368
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-82G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725368 | ||||||
| chr3:32725384
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.863-66A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725384 | ||||||
| chr3:32725413
|
A | G | 114 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.863-37A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725413 | ||||||
| chr3:32725783
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1012+184G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32725783 | ||||||
| chr3:32725885
|
T | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1012+286T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32725885 | ||||||
| chr3:32725920
|
T | G | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+321T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32725920 | ||||||
| chr3:32725927
|
A | AGTTTT | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 64 | HG00639.hp1 HG01106.hp2 HG01168.hp1 others(61): Show |
intron_variant | MODIFIER | c.1012+360_1012+364d others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | |||||
| chr3:32725927
|
A | AGTTTTGT others(3): Show |
87 | a0001c0001t0001g0040a0001c0001t0001g0079a0001c0001t0001g0080others(84): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1012+355_1012+364d others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | |||||
| chr3:32725927
|
A | AGTTTTGT others(8): Show |
2 | a0001c0001t0001g0155a0001c0001t0001g0326 | 2 | HG00558.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1012+350_1012+364d others(17): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | |||||
| chr3:32725927
|
A | AGTTTTGT others(13): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0190 | 2 | NA18961.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1012+345_1012+364d others(22): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | |||||
| chr3:32725927
|
AGTTTT | A | 114 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(111): Show | 114 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1012+360_1012+364d others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | |||||
| chr3:32725927
|
AGTTTTGT others(3): Show |
A | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+355_1012+364d others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | |||||
| chr3:32725927
|
AGTTTTGT others(8): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1012+350_1012+364d others(17): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | |||||
| chr3:32726059
|
T | C | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012+460T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726059 | ||||||
| chr3:32726142
|
A | G | 1 | a0001c0001t0003g0330 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1012+543A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726142 | ||||||
| chr3:32726248
|
A | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1012+649A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726248 | ||||||
| chr3:32726418
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1012+819G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726418 | ||||||
| chr3:32726477
|
G | T | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1012+878G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726477 | ||||||
| chr3:32726578
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1012+979C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726578 | ||||||
| chr3:32726631
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1012+1032G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726631 | ||||||
| chr3:32726693
|
CCAT | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1013-974_1013-972d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726693 | ||||||
| chr3:32726694
|
C | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0156 | 2 | HG01346.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1013-974C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726694 | ||||||
| chr3:32726694
|
C | CATA | 16 | a0001c0001t0001g0078a0001c0001t0001g0090a0001c0001t0001g0094others(13): Show | 16 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1013-939_1013-937d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | |||||
| chr3:32726694
|
C | CATAATA | 3 | a0001c0001t0001g0103a0001c0001t0001g0142a0001c0001t0003g0327 | 3 | HG01243.hp1 HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1013-942_1013-937d others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | |||||
| chr3:32726694
|
CATA | C | 67 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(64): Show | 67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1013-939_1013-937d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | |||||
| chr3:32726694
|
CATAATA | C | 106 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(103): Show | 106 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1013-942_1013-937d others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | |||||
| chr3:32726694
|
CATAATAA others(2): Show |
C | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1013-945_1013-937d others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | |||||
| chr3:32726836
|
A | AT | 11 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0001g0344others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1013-807dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | |||||
| chr3:32726836
|
AT | A | 49 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 49 | HG00438.hp2 HG00733.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1013-807delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | |||||
| chr3:32726836
|
ATT | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1013-808_1013-807d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | |||||
| chr3:32726836
|
ATTT | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0054others(6): Show | 9 | HG01099.hp1 HG01167.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1013-809_1013-807d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | |||||
| chr3:32726836
|
ATTTTTTT | A | 19 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(16): Show | 19 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.1013-813_1013-807d others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | |||||
| chr3:32726880
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1013-788C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726880 | ||||||
| chr3:32726902
|
A | G | 103 | a0001c0001t0001g0070a0001c0001t0001g0079a0001c0001t0001g0080others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1013-766A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726902 | ||||||
| chr3:32726972
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1013-696G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726972 | ||||||
| chr3:32727005
|
C | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1013-663C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727005 | ||||||
| chr3:32727021
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1013-647A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727021 | ||||||
| chr3:32727291
|
A | G | 258 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0066others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1013-377A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727291 | ||||||
| chr3:32727375
|
G | A | 3 | a0002c0002t0001g0269a0002c0002t0001g0272a0002c0002t0001g0273 | 3 | HG01081.hp1 HG01361.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1013-293G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727375 | ||||||
| chr3:32727396
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1013-272C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727396 | ||||||
| chr3:32727406
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1013-262C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727406 | ||||||
| chr3:32727933
|
T | TA | 10 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0086others(7): Show | 10 | HG01175.hp2 HG01243.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215+79dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727933 | |||||
| chr3:32727933
|
TA | T | 10 | a0001c0001t0001g0039a0001c0001t0001g0108a0001c0001t0001g0248others(7): Show | 10 | HG01257.hp1 HG01891.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.1215+79delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727933 | |||||
| chr3:32727945
|
A | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1215+75A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32727945 | ||||||
| chr3:32727979
|
T | TTTTA | 5 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0166others(2): Show | 5 | HG02630.hp1 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+137_1215+140d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | |||||
| chr3:32727979
|
T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0338a0001c0001t0002g0025a0001c0001t0002g0026others(1): Show | 4 | HG01891.hp2 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+133_1215+140d others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | |||||
| chr3:32727979
|
T | TTTTATTT others(5): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0339 | 2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1215+129_1215+140d others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | |||||
| chr3:32727979
|
T | TTTTATTT others(9): Show |
12 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215+125_1215+140d others(18): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | |||||
| chr3:32727979
|
T | TTTTATTT others(13): Show |
16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.1215+121_1215+140d others(22): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | |||||
| chr3:32727979
|
T | TTTTATTT others(17): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG02015.hp2 NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1215+117_1215+140d others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | |||||
| chr3:32727979
|
TTTTA | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+137_1215+140d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | |||||
| chr3:32727979
|
TTTTATTT others(5): Show |
T | 139 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(136): Show | 139 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.1215+129_1215+140d others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | |||||
| chr3:32728018
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1215+148C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728018 | ||||||
| chr3:32728099
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1215+229C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728099 | ||||||
| chr3:32728117
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1215+247C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728117 | ||||||
| chr3:32728160
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1215+290C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728160 | ||||||
| chr3:32728230
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1215+360A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728230 | ||||||
| chr3:32728276
|
G | A | 94 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(91): Show | 94 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1215+406G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728276 | ||||||
| chr3:32728361
|
C | G | 1 | a0001c0001t0001g0324 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1215+491C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728361 | ||||||
| chr3:32728391
|
C | T | 1 | a0002c0002t0001g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1215+521C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728391 | ||||||
| chr3:32728762
|
A | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1215+892A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728762 | ||||||
| chr3:32728783
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1215+913T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728783 | ||||||
| chr3:32728829
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1215+959C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728829 | ||||||
| chr3:32728857
|
T | G | 3 | a0001c0001t0001g0252a0001c0001t0001g0296a0001c0001t0001g0332 | 3 | HG02132.hp1 NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1215+987T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728857 | ||||||
| chr3:32728866
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | NA18960.hp2 NA18962.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+996C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728866 | ||||||
| chr3:32728897
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1215+1027G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728897 | ||||||
| chr3:32729012
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1215+1142C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729012 | ||||||
| chr3:32729053
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1215+1183G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729053 | ||||||
| chr3:32729148
|
A | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1215+1278A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729148 | ||||||
| chr3:32729425
|
G | A | 12 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215+1555G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729425 | ||||||
| chr3:32729586
|
G | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(2): Show | 5 | HG02615.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+1716G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729586 | ||||||
| chr3:32729669
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1215+1799T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729669 | ||||||
| chr3:32729744
|
G | C | 4 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0354others(1): Show | 4 | HG01106.hp1 HG01109.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+1874G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729744 | ||||||
| chr3:32729760
|
C | CT | 18 | a0001c0001t0001g0232a0001c0001t0001g0323a0001c0001t0001g0339others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1215+1916dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | |||||
| chr3:32729760
|
CT | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1215+1916delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | |||||
| chr3:32729760
|
CTT | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1215+1915_1215+191 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | |||||
| chr3:32729760
|
CTTT | C | 9 | a0001c0001t0001g0204a0001c0001t0001g0227a0001c0001t0001g0250others(6): Show | 9 | HG01928.hp2 HG02015.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215+1914_1215+191 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | |||||
| chr3:32729760
|
CTTTTTTT others(7): Show |
C | 11 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1215+1903_1215+191 others(18): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | |||||
| chr3:32729771
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1215+1901T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729771 | ||||||
| chr3:32729808
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1215+1938G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729808 | ||||||
| chr3:32729877
|
TC | T | 4 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0215others(1): Show | 4 | HG00639.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+2009delC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729877 | |||||
| chr3:32729908
|
A | C | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1215+2038A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729908 | ||||||
| chr3:32729918
|
G | A | 133 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0089others(130): Show | 133 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.1215+2048G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729918 | ||||||
| chr3:32730064
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG00558.hp2 NA18949.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1215+2194G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730064 | ||||||
| chr3:32730335
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1215+2465G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730335 | ||||||
| chr3:32730350
|
G | A | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0050others(7): Show | 10 | NA18947.hp1 NA18972.hp2 NA18985.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215+2480G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730350 | ||||||
| chr3:32730381
|
G | GT | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1215+2520dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32730381 | |||||
| chr3:32730623
|
C | T | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1215+2753C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730623 | ||||||
| chr3:32730948
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1216-2475T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730948 | ||||||
| chr3:32730950
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1216-2473A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730950 | ||||||
| chr3:32731241
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1216-2182G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731241 | ||||||
| chr3:32731278
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1216-2145C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731278 | ||||||
| chr3:32731489
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1216-1934T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731489 | ||||||
| chr3:32731630
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-1793C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731630 | ||||||
| chr3:32731731
|
C | A | 1 | a0001c0001t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1216-1692C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731731 | ||||||
| chr3:32731815
|
A | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1216-1608A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731815 | ||||||
| chr3:32732081
|
A | G | 118 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1216-1342A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732081 | ||||||
| chr3:32732117
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1216-1306G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732117 | ||||||
| chr3:32732338
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG00558.hp2 NA18949.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1216-1085C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732338 | ||||||
| chr3:32732350
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | NA18945.hp1 NA18955.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-1073G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732350 | ||||||
| chr3:32732490
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1216-933G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732490 | ||||||
| chr3:32732606
|
G | GA | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1216-806dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32732606 | |||||
| chr3:32732626
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1216-797C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732626 | ||||||
| chr3:32732938
|
T | G | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1216-485T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732938 | ||||||
| chr3:32732980
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1216-443A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732980 | ||||||
| chr3:32733036
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1216-387A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733036 | ||||||
| chr3:32733191
|
C | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0156a0001c0001t0001g0197 | 3 | HG02970.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1216-232C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733191 | ||||||
| chr3:32733262
|
T | C | 144 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(141): Show | 144 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.1216-161T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733262 | ||||||
| chr3:32733290
|
A | G | 259 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1216-133A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733290 | ||||||
| chr3:32733398
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1216-25A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733398 | ||||||
| chr3:32733566
|
A | T | 1 | a0001c0001t0001g0052 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1337+22A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32733566 | ||||||
| chr3:32733593
|
CATA | C | 10 | a0001c0001t0001g0204a0001c0001t0001g0227a0001c0001t0001g0250others(7): Show | 10 | HG01928.hp2 HG02015.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337+52_1337+54del others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 32733593 | |||||
| chr3:32733675
|
A | T | 1 | a0001c0001t0001g0303 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1337+131A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32733675 | ||||||
| chr3:32734369
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1338-431T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32734369 | ||||||
| chr3:32734507
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1338-293G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32734507 | ||||||
| chr3:32734599
|
C | CAATCCAT others(6): Show |
1 | a0001c0001t0001g0301 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1338-200_1338-188d others(15): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 32734599 | |||||
| chr3:32734599
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1338-201C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32734599 | ||||||
| chr3:32734740
|
A | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1338-60A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32734740 | ||||||
| chr3:32735318
|
T | C | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1514+342T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735318 | ||||||
| chr3:32735320
|
T | G | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1514+344T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735320 | ||||||
| chr3:32735324
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1514+348G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735324 | ||||||
| chr3:32735330
|
G | GCGAGACT others(31): Show |
21 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(18): Show | 21 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.1514+354_1514+355i others(40): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735330 | ||||||
| chr3:32735330
|
G | GCGAGACT others(32): Show |
2 | a0001c0001t0001g0217a0001c0001t0001g0222 | 2 | HG03516.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1514+354_1514+355i others(41): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735330 | ||||||
| chr3:32735331
|
T | A | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1514+355T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735331 | ||||||
| chr3:32735369
|
T | C | 3 | a0001c0001t0001g0249a0001c0001t0001g0295a0001c0001t0001g0308 | 3 | HG01167.hp2 HG01169.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1514+393T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735369 | ||||||
| chr3:32735581
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1514+605C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735581 | ||||||
| chr3:32735589
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1514+613C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735589 | ||||||
| chr3:32735658
|
G | A | 14 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(11): Show | 14 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1514+682G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735658 | ||||||
| chr3:32735797
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1514+821A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735797 | ||||||
| chr3:32736025
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1514+1049A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736025 | ||||||
| chr3:32736082
|
T | TTTTG | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1514+1122_1514+112 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 32736082 | |||||
| chr3:32736142
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1514+1166G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736142 | ||||||
| chr3:32736160
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1514+1184A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736160 | ||||||
| chr3:32736166
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1514+1190A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736166 | ||||||
| chr3:32736204
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1515-1206A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736204 | ||||||
| chr3:32736207
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1515-1203C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736207 | ||||||
| chr3:32736339
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0326 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1515-1071G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736339 | ||||||
| chr3:32736415
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1515-995G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736415 | ||||||
| chr3:32736556
|
C | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1515-854C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736556 | ||||||
| chr3:32736676
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1515-734G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736676 | ||||||
| chr3:32736724
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1515-686A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736724 | ||||||
| chr3:32736831
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515-579C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736831 | ||||||
| chr3:32736915
|
G | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0203 | 2 | NA18979.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1515-495G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736915 | ||||||
| chr3:32737009
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515-401T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737009 | ||||||
| chr3:32737034
|
C | T | 3 | a0002c0002t0001g0269a0002c0002t0001g0272a0002c0002t0001g0273 | 3 | HG01081.hp1 HG01361.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1515-376C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737034 | ||||||
| chr3:32737104
|
G | A | 346 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(343): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1515-306G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737104 | ||||||
| chr3:32737221
|
G | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1515-189G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737221 | ||||||
| chr3:32737245
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515-165G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737245 | ||||||
| chr3:32737270
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1515-140G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737270 | ||||||
| chr3:32737283
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1515-127C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737283 | ||||||
| chr3:32737795
|
A | T | 144 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(141): Show | 144 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.1595+305A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32737795 | ||||||
| chr3:32737809
|
A | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1595+319A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32737809 | ||||||
| chr3:32737951
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+461T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32737951 | ||||||
| chr3:32738003
|
A | G | 4 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0066others(1): Show | 4 | NA18981.hp2 NA18989.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+513A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738003 | ||||||
| chr3:32738156
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+666G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738156 | ||||||
| chr3:32738191
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0222 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1595+701G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738191 | ||||||
| chr3:32738324
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+834A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738324 | ||||||
| chr3:32738336
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1595+846T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738336 | ||||||
| chr3:32738465
|
C | CT | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(9): Show | 12 | HG01891.hp2 HG01981.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1595+990dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32738465 | |||||
| chr3:32738465
|
CT | C | 53 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1595+990delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32738465 | |||||
| chr3:32738493
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00408.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1595+1003C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738493 | ||||||
| chr3:32738590
|
G | A | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1595+1100G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738590 | ||||||
| chr3:32738608
|
G | A | 11 | a0001c0001t0001g0210a0001c0001t0001g0217a0001c0001t0001g0218others(8): Show | 11 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1595+1118G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738608 | ||||||
| chr3:32738652
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1595+1162C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738652 | ||||||
| chr3:32738664
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+1174G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738664 | ||||||
| chr3:32738684
|
G | T | 1 | a0001c0001t0001g0302 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1595+1194G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738684 | ||||||
| chr3:32738695
|
G | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+1205G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738695 | ||||||
| chr3:32738757
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+1267C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738757 | ||||||
| chr3:32738785
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+1295G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738785 | ||||||
| chr3:32738905
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1595+1415T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738905 | ||||||
| chr3:32738951
|
G | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+1461G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738951 | ||||||
| chr3:32738954
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1595+1464G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738954 | ||||||
| chr3:32739125
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1595+1635C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739125 | ||||||
| chr3:32739201
|
C | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+1711C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739201 | ||||||
| chr3:32739239
|
C | G | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1595+1749C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739239 | ||||||
| chr3:32739350
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+1860T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739350 | ||||||
| chr3:32739404
|
A | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+1914A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739404 | ||||||
| chr3:32739519
|
C | CT | 8 | a0001c0001t0001g0082a0001c0001t0001g0237a0001c0001t0001g0240others(5): Show | 8 | HG01099.hp1 HG01168.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1595+2037dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32739519 | |||||
| chr3:32739519
|
CT | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+2037delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32739519 | |||||
| chr3:32739533
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+2043T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739533 | ||||||
| chr3:32739621
|
T | TA | 105 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(102): Show | 105 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1595+2138dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32739621 | |||||
| chr3:32739755
|
T | C | 20 | a0001c0001t0001g0210a0001c0001t0001g0217a0001c0001t0001g0218others(17): Show | 20 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.1595+2265T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739755 | ||||||
| chr3:32739777
|
T | G | 1 | a0001c0001t0001g0301 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1595+2287T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739777 | ||||||
| chr3:32739894
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1595+2404C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739894 | ||||||
| chr3:32740033
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+2543G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740033 | ||||||
| chr3:32740058
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+2568T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740058 | ||||||
| chr3:32740073
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1595+2583G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740073 | ||||||
| chr3:32740080
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1595+2590G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740080 | ||||||
| chr3:32740153
|
G | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+2663G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740153 | ||||||
| chr3:32740227
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1595+2737G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740227 | ||||||
| chr3:32740242
|
C | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+2752C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740242 | ||||||
| chr3:32740299
|
A | C | 122 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1595+2809A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740299 | ||||||
| chr3:32740304
|
C | A | 106 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(103): Show | 106 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1595+2814C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740304 | ||||||
| chr3:32740432
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+2942A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740432 | ||||||
| chr3:32740463
|
A | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+2973A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740463 | ||||||
| chr3:32740629
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+3139G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740629 | ||||||
| chr3:32740637
|
T | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1595+3147T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740637 | ||||||
| chr3:32740643
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1595+3153A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740643 | ||||||
| chr3:32740682
|
G | A | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1595+3192G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740682 | ||||||
| chr3:32740744
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1595+3254C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740744 | ||||||
| chr3:32740840
|
C | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+3350C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740840 | ||||||
| chr3:32740841
|
G | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+3351G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740841 | ||||||
| chr3:32740861
|
T | TA | 30 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(27): Show | 30 | HG01169.hp1 HG01243.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1595+3391dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32740861 | |||||
| chr3:32740861
|
TA | T | 118 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0052others(115): Show | 118 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.1595+3391delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32740861 | |||||
| chr3:32740861
|
TAA | T | 6 | a0001c0001t0001g0224a0001c0001t0001g0239a0001c0001t0001g0242others(3): Show | 6 | HG00408.hp2 HG01169.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595+3390_1595+339 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32740861 | |||||
| chr3:32741052
|
T | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1595+3562T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741052 | ||||||
| chr3:32741336
|
TATTCC | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1595+3853_1595+385 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741336 | |||||
| chr3:32741541
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+4051G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741541 | ||||||
| chr3:32741544
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4054C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741544 | ||||||
| chr3:32741716
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1595+4226C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741716 | ||||||
| chr3:32741756
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1595+4266G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741756 | ||||||
| chr3:32741768
|
C | CA | 22 | a0001c0001t0001g0039a0001c0001t0001g0067a0001c0001t0001g0078others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4293dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741768
|
C | CAAAAAAA | 8 | a0001c0001t0001g0338a0001c0001t0001g0345a0001c0001t0001g0347others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1595+4287_1595+429 others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741768
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1595+4284_1595+429 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741768
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+4283_1595+429 others(15): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741768
|
C | CAAAAAAA others(10): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0020others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1595+4293_1595+429 others(21): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741768
|
C | CAAAAAAA others(11): Show |
10 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(7): Show | 10 | HG02015.hp2 HG02602.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1595+4293_1595+429 others(22): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741768
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(1): Show | 4 | HG02132.hp2 NA18963.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+4293_1595+429 others(23): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741768
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0014 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1595+4293_1595+429 others(24): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741768
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0013 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1595+4293_1595+429 others(25): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | |||||
| chr3:32741852
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+4362G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741852 | ||||||
| chr3:32741857
|
A | C | 5 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1595+4367A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741857 | ||||||
| chr3:32741860
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+4370G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741860 | ||||||
| chr3:32741983
|
A | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+4493A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741983 | ||||||
| chr3:32741984
|
T | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+4494T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741984 | ||||||
| chr3:32741988
|
A | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1595+4498A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741988 | ||||||
| chr3:32741990
|
T | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4500T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741990 | ||||||
| chr3:32742088
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1595+4598T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742088 | ||||||
| chr3:32742139
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1595+4649A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742139 | ||||||
| chr3:32742196
|
C | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+4706C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742196 | ||||||
| chr3:32742301
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4811A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742301 | ||||||
| chr3:32742318
|
A | C | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0277others(3): Show | 6 | HG01074.hp2 HG01496.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1595+4828A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742318 | ||||||
| chr3:32742363
|
T | C | 4 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG00642.hp1 HG01517.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+4873T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742363 | ||||||
| chr3:32742393
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 91 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1595+4903C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742393 | ||||||
| chr3:32742483
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4993G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742483 | ||||||
| chr3:32742491
|
C | CA | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+5002dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32742491 | |||||
| chr3:32742550
|
T | C | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1595+5060T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742550 | ||||||
| chr3:32742655
|
C | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1595+5165C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742655 | ||||||
| chr3:32742984
|
C | CT | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(136): Show | 139 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.1595+5513dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32742984 | |||||
| chr3:32742984
|
CT | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0046others(3): Show | 6 | HG01074.hp1 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595+5513delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32742984 | |||||
| chr3:32743010
|
G | T | 11 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1595+5520G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743010 | ||||||
| chr3:32743019
|
C | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+5529C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743019 | ||||||
| chr3:32743025
|
T | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1595+5535T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743025 | ||||||
| chr3:32743026
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+5536C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743026 | ||||||
| chr3:32743140
|
C | T | 4 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0270others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+5650C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743140 | ||||||
| chr3:32743294
|
A | G | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+5804A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743294 | ||||||
| chr3:32743343
|
G | T | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+5853G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743343 | ||||||
| chr3:32743368
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+5878G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743368 | ||||||
| chr3:32743410
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+5920G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743410 | ||||||
| chr3:32743422
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0222 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1595+5932G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743422 | ||||||
| chr3:32743427
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1595+5937C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743427 | ||||||
| chr3:32743524
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+6034C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743524 | ||||||
| chr3:32743525
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+6035A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743525 | ||||||
| chr3:32743526
|
C | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+6036C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743526 | ||||||
| chr3:32743625
|
C | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1595+6135C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743625 | ||||||
| chr3:32743645
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1595+6155C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743645 | ||||||
| chr3:32743679
|
A | G | 5 | a0001c0001t0001g0237a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 5 | HG01099.hp1 HG01168.hp2 NA20752.hp2 others(2): Show |
intron_variant | MODIFIER | c.1595+6189A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743679 | ||||||
| chr3:32743726
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1595+6236A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743726 | ||||||
| chr3:32743752
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1595+6262G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743752 | ||||||
| chr3:32743789
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1595+6299A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743789 | ||||||
| chr3:32743806
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1595+6316A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743806 | ||||||
| chr3:32743857
|
T | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+6367T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743857 | ||||||
| chr3:32743863
|
T | G | 349 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(346): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+6373T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743863 | ||||||
| chr3:32743904
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+6414G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743904 | ||||||
| chr3:32743906
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG02004.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1595+6416C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743906 | ||||||
| chr3:32743938
|
G | GTA | 4 | a0001c0001t0001g0183a0001c0001t0001g0252a0001c0001t0001g0296others(1): Show | 4 | HG02132.hp1 NA18943.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+6458_1595+645 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32743938 | |||||
| chr3:32744036
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0287 | 2 | HG01258.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1595+6546A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744036 | ||||||
| chr3:32744284
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+6794G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744284 | ||||||
| chr3:32744379
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+6889A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744379 | ||||||
| chr3:32744556
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1595+7066A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744556 | ||||||
| chr3:32744571
|
G | A | 4 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0215others(1): Show | 4 | HG00639.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+7081G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744571 | ||||||
| chr3:32744771
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0167 | 2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1595+7281C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744771 | ||||||
| chr3:32744898
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1595+7408G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744898 | ||||||
| chr3:32745068
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1595+7578G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745068 | ||||||
| chr3:32745214
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1595+7724T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745214 | ||||||
| chr3:32745264
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+7774T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745264 | ||||||
| chr3:32745266
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+7776G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745266 | ||||||
| chr3:32745275
|
T | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+7785T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745275 | ||||||
| chr3:32745392
|
A | G | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1595+7902A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745392 | ||||||
| chr3:32745469
|
A | AGATAACA others(3): Show |
350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1595+7979_1595+798 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745469 | ||||||
| chr3:32745471
|
T | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1595+7981T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745471 | ||||||
| chr3:32745472
|
G | A | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1595+7982G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745472 | ||||||
| chr3:32745473
|
A | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1595+7983A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745473 | ||||||
| chr3:32745475
|
T | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1595+7985T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745475 | ||||||
| chr3:32745488
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+7998C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745488 | ||||||
| chr3:32745707
|
G | GA | 5 | a0001c0001t0001g0338a0001c0001t0001g0341a0001c0001t0001g0342others(2): Show | 5 | HG01891.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1595+8219dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32745707 | |||||
| chr3:32745830
|
CTG | C | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+8342_1595+834 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32745830 | |||||
| chr3:32746038
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0326 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1595+8548A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746038 | ||||||
| chr3:32746055
|
T | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1595+8565T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746055 | ||||||
| chr3:32746148
|
T | C | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1595+8658T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746148 | ||||||
| chr3:32746279
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1595+8789A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746279 | ||||||
| chr3:32746538
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1595+9048G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746538 | ||||||
| chr3:32746664
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+9174G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746664 | ||||||
| chr3:32746698
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+9208G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746698 | ||||||
| chr3:32746757
|
T | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+9267T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746757 | ||||||
| chr3:32746815
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1595+9325C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746815 | ||||||
| chr3:32746832
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+9342G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746832 | ||||||
| chr3:32746836
|
C | CA | 7 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0119others(4): Show | 7 | HG00735.hp2 HG00738.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1595+9367dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32746836 | |||||
| chr3:32746836
|
CA | C | 154 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(151): Show | 154 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1595+9367delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32746836 | |||||
| chr3:32746836
|
CAA | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0034others(32): Show | 35 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1595+9366_1595+936 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32746836 | |||||
| chr3:32746836
|
CAAAAA | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1595+9363_1595+936 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32746836 | |||||
| chr3:32746960
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1595+9470A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746960 | ||||||
| chr3:32747014
|
G | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1595+9524G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747014 | ||||||
| chr3:32747093
|
G | A | 4 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0215others(1): Show | 4 | HG00639.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+9603G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747093 | ||||||
| chr3:32747201
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1595+9711A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747201 | ||||||
| chr3:32747276
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1595+9786G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747276 | ||||||
| chr3:32747307
|
A | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+9817A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747307 | ||||||
| chr3:32747355
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+9865G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747355 | ||||||
| chr3:32747450
|
A | T | 1 | a0001c0001t0001g0347 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1595+9960A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747450 | ||||||
| chr3:32747451
|
T | A | 1 | a0001c0001t0001g0347 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1595+9961T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747451 | ||||||
| chr3:32747634
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+10144G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747634 | ||||||
| chr3:32747694
|
A | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0005g0031 | 3 | HG02572.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1595+10204A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747694 | ||||||
| chr3:32747731
|
C | G | 1 | a0001c0001t0001g0288 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1595+10241C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747731 | ||||||
| chr3:32747745
|
G | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+10255G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747745 | ||||||
| chr3:32747808
|
C | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1595+10318C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747808 | ||||||
| chr3:32747854
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+10364G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747854 | ||||||
| chr3:32747889
|
A | G | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1595+10399A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747889 | ||||||
| chr3:32747905
|
G | GCCAC | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+10416_1595+10 others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32747905 | |||||
| chr3:32747964
|
C | CA | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+10483dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32747964 | |||||
| chr3:32747990
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1595+10500C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747990 | ||||||
| chr3:32748027
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1595+10537A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748027 | ||||||
| chr3:32748422
|
T | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+10932T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748422 | ||||||
| chr3:32748461
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+10971A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748461 | ||||||
| chr3:32748485
|
A | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-10973A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748485 | ||||||
| chr3:32748605
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-10853C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748605 | ||||||
| chr3:32748637
|
C | T | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-10821C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748637 | ||||||
| chr3:32748669
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-10789C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748669 | ||||||
| chr3:32748907
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-10551C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748907 | ||||||
| chr3:32748914
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-10544C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748914 | ||||||
| chr3:32748923
|
G | T | 1 | a0001c0001t0001g0345 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1596-10535G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748923 | ||||||
| chr3:32748968
|
T | C | 107 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(104): Show | 107 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1596-10490T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748968 | ||||||
| chr3:32749008
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-10450G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749008 | ||||||
| chr3:32749192
|
G | C | 1 | a0001c0001t0001g0251 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1596-10266G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749192 | ||||||
| chr3:32749216
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1596-10242G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749216 | ||||||
| chr3:32749261
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596-10197T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749261 | ||||||
| chr3:32749278
|
C | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-10180C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749278 | ||||||
| chr3:32749405
|
A | AT | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-10032dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | |||||
| chr3:32749405
|
A | ATT | 14 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596-10033_1596-10 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | |||||
| chr3:32749405
|
A | ATTT | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(19): Show | 22 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1596-10034_1596-10 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | |||||
| chr3:32749405
|
AT | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(268): Show | 271 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1596-10032delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | |||||
| chr3:32749405
|
ATT | A | 15 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0047others(12): Show | 15 | HG00558.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-10033_1596-10 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | |||||
| chr3:32749446
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1596-10012A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749446 | ||||||
| chr3:32749479
|
G | A | 11 | a0001c0001t0001g0210a0001c0001t0001g0217a0001c0001t0001g0218others(8): Show | 11 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596-9979G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749479 | ||||||
| chr3:32749645
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-9813G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749645 | ||||||
| chr3:32749843
|
G | C | 11 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596-9615G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749843 | ||||||
| chr3:32749994
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-9464A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749994 | ||||||
| chr3:32750091
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1596-9367T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750091 | ||||||
| chr3:32750235
|
C | A | 1 | a0001c0001t0001g0005 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1596-9223C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750235 | ||||||
| chr3:32750240
|
A | T | 1 | a0001c0001t0001g0005 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1596-9218A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750240 | ||||||
| chr3:32750384
|
A | T | 5 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-9074A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750384 | ||||||
| chr3:32750424
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1596-9034C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750424 | ||||||
| chr3:32750467
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1596-8991G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750467 | ||||||
| chr3:32750580
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1596-8878T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750580 | ||||||
| chr3:32750712
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1596-8746C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750712 | ||||||
| chr3:32750738
|
G | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1596-8720G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750738 | ||||||
| chr3:32750757
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-8701G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750757 | ||||||
| chr3:32750768
|
T | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0134 | 2 | HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1596-8690T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750768 | ||||||
| chr3:32750786
|
G | A | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-8672G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750786 | ||||||
| chr3:32750839
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0275 | 2 | HG00738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1596-8619C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750839 | ||||||
| chr3:32750858
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1596-8600A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750858 | ||||||
| chr3:32750900
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1596-8558T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750900 | ||||||
| chr3:32750910
|
C | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG01168.hp1 HG01169.hp1 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.1596-8548C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750910 | ||||||
| chr3:32751056
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1596-8402G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751056 | ||||||
| chr3:32751101
|
GA | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-8348delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32751101 | |||||
| chr3:32751111
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0088 | 2 | NA18951.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1596-8347T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751111 | ||||||
| chr3:32751133
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0298 | 2 | HG00733.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1596-8325C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751133 | ||||||
| chr3:32751164
|
A | G | 6 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0043others(3): Show | 6 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596-8294A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751164 | ||||||
| chr3:32751230
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-8228A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751230 | ||||||
| chr3:32751274
|
A | AT | 9 | a0001c0001t0001g0102a0001c0001t0001g0119a0001c0001t0001g0267others(6): Show | 9 | HG00140.hp1 HG01981.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596-8172dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32751274 | |||||
| chr3:32751294
|
CAG | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-8161_1596-816 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32751294 | |||||
| chr3:32751311
|
G | A | 1 | a0002c0002t0001g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596-8147G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751311 | ||||||
| chr3:32751341
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1596-8117A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751341 | ||||||
| chr3:32751456
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1596-8002A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751456 | ||||||
| chr3:32751776
|
T | C | 7 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(4): Show | 7 | HG00735.hp1 HG01071.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596-7682T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751776 | ||||||
| chr3:32751816
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1596-7642G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751816 | ||||||
| chr3:32751978
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0310 | 2 | HG00741.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1596-7480T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751978 | ||||||
| chr3:32752035
|
T | C | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596-7423T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752035 | ||||||
| chr3:32752086
|
CG | C | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-7369delG | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32752086 | |||||
| chr3:32752506
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-6952G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752506 | ||||||
| chr3:32752561
|
A | G | 111 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(108): Show | 111 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1596-6897A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752561 | ||||||
| chr3:32752591
|
A | G | 15 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-6867A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752591 | ||||||
| chr3:32752814
|
A | T | 1 | a0001c0001t0001g0301 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1596-6644A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752814 | ||||||
| chr3:32752841
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-6617C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752841 | ||||||
| chr3:32752978
|
C | T | 1 | a0002c0002t0001g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596-6480C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752978 | ||||||
| chr3:32753047
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1596-6411A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753047 | ||||||
| chr3:32753106
|
T | C | 105 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(102): Show | 105 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1596-6352T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753106 | ||||||
| chr3:32753142
|
C | T | 10 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0345others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596-6316C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753142 | ||||||
| chr3:32753290
|
C | A | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-6168C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753290 | ||||||
| chr3:32753314
|
C | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0280 | 3 | HG02004.hp1 HG02109.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1596-6144C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753314 | ||||||
| chr3:32753539
|
A | C | 9 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596-5919A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753539 | ||||||
| chr3:32753667
|
G | A | 1 | a0001c0001t0003g0330 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1596-5791G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753667 | ||||||
| chr3:32753725
|
C | T | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-5733C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753725 | ||||||
| chr3:32753873
|
CTGA | C | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596-5580_1596-557 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32753873 | |||||
| chr3:32753918
|
T | TCA | 18 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0326others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596-5523_1596-552 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32753918 | |||||
| chr3:32753918
|
T | TCACA | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1596-5525_1596-552 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32753918 | |||||
| chr3:32754083
|
A | C | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-5375A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754083 | ||||||
| chr3:32754086
|
G | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0307 | 2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1596-5372G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754086 | ||||||
| chr3:32754108
|
A | G | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1596-5350A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754108 | ||||||
| chr3:32754159
|
G | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596-5299G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754159 | ||||||
| chr3:32754222
|
A | G | 1 | a0001c0001t0001g0345 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1596-5236A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754222 | ||||||
| chr3:32754260
|
G | A | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-5198G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754260 | ||||||
| chr3:32754274
|
G | A | 142 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(139): Show | 142 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.1596-5184G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754274 | ||||||
| chr3:32754321
|
C | T | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-5137C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754321 | ||||||
| chr3:32754392
|
G | A | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-5066G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754392 | ||||||
| chr3:32754406
|
G | A | 8 | a0001c0001t0001g0228a0001c0001t0001g0236a0001c0001t0001g0253others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596-5052G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754406 | ||||||
| chr3:32754414
|
T | G | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596-5044T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754414 | ||||||
| chr3:32754464
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-4994A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754464 | ||||||
| chr3:32754472
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0050others(2): Show | 5 | NA18972.hp2 NA18985.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596-4986G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754472 | ||||||
| chr3:32754476
|
C | CA | 45 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(42): Show | 45 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1596-4968dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754476 | |||||
| chr3:32754476
|
C | CAA | 8 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0043others(5): Show | 8 | HG00741.hp2 HG02572.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-4969_1596-496 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754476 | |||||
| chr3:32754476
|
CAA | C | 10 | a0001c0001t0001g0107a0001c0001t0001g0339a0001c0001t0001g0345others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596-4969_1596-496 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754476 | |||||
| chr3:32754476
|
CAAA | C | 12 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596-4970_1596-496 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754476 | |||||
| chr3:32754485
|
A | ATAT | 8 | a0001c0001t0001g0121a0001c0001t0001g0245a0001c0001t0001g0249others(5): Show | 8 | HG01361.hp2 HG01433.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-4973_1596-497 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754485 | ||||||
| chr3:32754487
|
A | AAT | 12 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0217others(9): Show | 12 | HG01515.hp1 HG01517.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596-4970_1596-496 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754487 | |||||
| chr3:32754487
|
A | ATAT | 62 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0091others(59): Show | 62 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1596-4971_1596-497 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754487 | ||||||
| chr3:32754487
|
A | ATATAT | 5 | a0001c0001t0001g0188a0001c0001t0001g0228a0001c0001t0001g0238others(2): Show | 5 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-4971_1596-497 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754487 | ||||||
| chr3:32754487
|
A | ATATATAT | 7 | a0001c0001t0001g0250a0001c0001t0001g0261a0001c0001t0001g0282others(4): Show | 7 | NA18945.hp2 NA18950.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596-4971_1596-497 others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754487 | ||||||
| chr3:32754487
|
A | T | 12 | a0001c0001t0001g0101a0001c0001t0001g0104a0001c0001t0001g0121others(9): Show | 12 | HG01257.hp2 HG01361.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596-4971A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754487 | ||||||
| chr3:32754489
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(34): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(36): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0080 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(27): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(26): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0131a0001c0001t0001g0150 | 3 | HG01943.hp1 HG02027.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(37): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0001g0333 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(43): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0173 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(20): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0195 | 2 | HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(24): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0194 | 2 | HG01358.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0172a0001c0001t0001g0177 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(23): Show |
3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0198 | 3 | NA18946.hp1 NA18974.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(34): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0331 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(40): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(25): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0170 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(29): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(20): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0120 | 2 | HG02135.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(31): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0001g0191 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(37): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(39): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(15): Show |
5 | a0001c0001t0001g0085a0001c0001t0001g0123a0001c0001t0001g0133others(2): Show | 5 | HG00099.hp2 HG01975.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(28): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0200 | 3 | NA18967.hp2 NA18982.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(32): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(36): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(27): Show |
4 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0190others(1): Show | 4 | HG00673.hp1 NA18961.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(38): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0135a0001c0001t0001g0193 | 2 | HG02300.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(40): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(31): Show |
3 | a0001c0001t0001g0125a0001c0001t0001g0174a0001c0001t0001g0175 | 3 | NA18945.hp1 NA18972.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(42): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(33): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0168 | 2 | HG02155.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(44): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0159 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(46): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAT others(22): Show |
1 | a0001c0001t0001g0169 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(33): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAT others(24): Show |
1 | a0001c0001t0001g0132 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(35): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAT others(26): Show |
1 | a0001c0001t0001g0140 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(37): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAAAT others(32): Show |
2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(43): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(13): Show |
1 | a0001c0001t0001g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(24): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(15): Show |
8 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG02809.hp1 HG02970.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(17): Show |
1 | a0001c0001t0001g0156 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(28): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(19): Show |
1 | a0001c0001t0001g0196 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(21): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0176a0001c0001t0001g0337 | 3 | HG01081.hp2 HG02559.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(32): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(23): Show |
3 | a0001c0001t0001g0166a0001c0001t0001g0182a0001c0001t0001g0202 | 3 | HG00438.hp2 HG02630.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(34): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(25): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG03669.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(36): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(27): Show |
6 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0001g0149others(3): Show | 6 | HG01433.hp2 NA18979.hp2 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(38): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAAATA others(33): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0158 | 2 | HG00323.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(44): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAATAT others(20): Show |
2 | a0001c0001t0001g0178a0001c0003t0001g0145 | 2 | HG02083.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(31): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAATAT others(24): Show |
1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(35): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAAATAT others(26): Show |
1 | a0001c0001t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(37): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAATATA others(1): Show |
17 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(14): Show | 17 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAATATA others(3): Show |
3 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0216 | 3 | HG00639.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(24): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAATATA others(15): Show |
1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAAATATA others(19): Show |
1 | a0001c0001t0001g0141 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAATATAT others(22): Show |
1 | a0001c0001t0001g0163 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(33): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AAATATAT others(34): Show |
1 | a0001c0001t0001g0134 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(45): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AATATATA others(19): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0129 | 2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1596-4966_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | AATATATA others(21): Show |
1 | a0001c0001t0003g0327 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596-4966_1596-496 others(32): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | |||||
| chr3:32754489
|
A | ATAT | 24 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0105others(21): Show | 24 | HG00738.hp1 HG01071.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596-4969_1596-496 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754489 | ||||||
| chr3:32754489
|
A | ATATAT | 7 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(4): Show | 7 | HG00733.hp2 HG01069.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596-4969_1596-496 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754489 | ||||||
| chr3:32754489
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1596-4969_1596-496 others(33): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754489 | ||||||
| chr3:32754489
|
A | T | 114 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1596-4969A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754489 | ||||||
| chr3:32754490
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0119 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(38): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754490 | ||||||
| chr3:32754491
|
T | A | 42 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1596-4967T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754491 | ||||||
| chr3:32754491
|
TAC | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-4965_1596-496 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754491 | |||||
| chr3:32754493
|
C | T | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1596-4965C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754493 | ||||||
| chr3:32754495
|
T | A | 1 | a0001c0001t0001g0184 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596-4963T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754495 | ||||||
| chr3:32754497
|
T | A | 1 | a0001c0001t0001g0184 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596-4961T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754497 | ||||||
| chr3:32754506
|
A | T | 13 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(10): Show | 13 | HG01081.hp1 HG01361.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596-4952A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754506 | ||||||
| chr3:32754518
|
C | CT | 151 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1596-4921dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754518 | |||||
| chr3:32754518
|
C | CTT | 17 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0063others(14): Show | 17 | HG00673.hp1 HG01358.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.1596-4922_1596-492 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754518 | |||||
| chr3:32754518
|
CT | C | 17 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0342others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1596-4921delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754518 | |||||
| chr3:32754518
|
CTTTTTT | C | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1596-4926_1596-492 others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754518 | |||||
| chr3:32754565
|
G | A | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-4893G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754565 | ||||||
| chr3:32754644
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1596-4814T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754644 | ||||||
| chr3:32754673
|
T | C | 351 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1596-4785T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754673 | ||||||
| chr3:32754690
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0303 | 2 | HG02148.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1596-4768T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754690 | ||||||
| chr3:32754698
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596-4760T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754698 | ||||||
| chr3:32754710
|
C | G | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-4748C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754710 | ||||||
| chr3:32754710
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0110 | 2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1596-4748C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754710 | ||||||
| chr3:32754752
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1596-4706T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754752 | ||||||
| chr3:32754846
|
C | T | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-4612C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754846 | ||||||
| chr3:32754897
|
C | CA | 17 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0092others(14): Show | 17 | HG01074.hp2 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-4547dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754897 | |||||
| chr3:32754897
|
C | CAAA | 9 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0347others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596-4549_1596-454 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754897 | |||||
| chr3:32754897
|
C | CAAAA | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596-4550_1596-454 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754897 | |||||
| chr3:32754968
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1596-4490C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754968 | ||||||
| chr3:32754969
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1596-4489G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754969 | ||||||
| chr3:32755034
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1596-4424G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755034 | ||||||
| chr3:32755126
|
G | A | 98 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1596-4332G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755126 | ||||||
| chr3:32755171
|
G | A | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596-4287G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755171 | ||||||
| chr3:32755248
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-4210A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755248 | ||||||
| chr3:32755295
|
A | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-4163A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755295 | ||||||
| chr3:32755319
|
C | CT | 13 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0065others(10): Show | 13 | HG00438.hp2 HG01106.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596-4123dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755319 | |||||
| chr3:32755319
|
C | CTTT | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(17): Show | 20 | HG01168.hp1 HG01169.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.1596-4125_1596-412 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755319 | |||||
| chr3:32755319
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0121 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1596-4132_1596-412 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755319 | |||||
| chr3:32755325
|
T | C | 20 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1596-4133T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755325 | ||||||
| chr3:32755341
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-4117A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755341 | ||||||
| chr3:32755544
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1596-3914A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755544 | ||||||
| chr3:32755587
|
A | T | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-3871A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755587 | ||||||
| chr3:32755757
|
C | CTT | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-3688_1596-368 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755757 | |||||
| chr3:32755757
|
CT | C | 117 | a0001c0001t0001g0039a0001c0001t0001g0078a0001c0001t0001g0079others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1596-3687delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755757 | |||||
| chr3:32755803
|
G | C | 1 | a0001c0001t0001g0336 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1596-3655G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755803 | ||||||
| chr3:32755849
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0005g0031 | 3 | HG02572.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1596-3609A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755849 | ||||||
| chr3:32755851
|
TG | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-3603delG | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755851 | |||||
| chr3:32756038
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1596-3420G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756038 | ||||||
| chr3:32756313
|
G | A | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-3145G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756313 | ||||||
| chr3:32756315
|
C | A | 98 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1596-3143C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756315 | ||||||
| chr3:32756332
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1596-3126T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756332 | ||||||
| chr3:32756382
|
G | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0268a0001c0001t0001g0307 | 3 | HG01243.hp2 HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1596-3076G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756382 | ||||||
| chr3:32756577
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-2881A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756577 | ||||||
| chr3:32756621
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1596-2837C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756621 | ||||||
| chr3:32756697
|
T | C | 19 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0114others(16): Show | 19 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596-2761T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756697 | ||||||
| chr3:32756879
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596-2579C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756879 | ||||||
| chr3:32756904
|
T | TGAGA | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-2554_1596-255 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756904 | ||||||
| chr3:32756921
|
A | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-2537A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756921 | ||||||
| chr3:32756979
|
A | G | 351 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1596-2479A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756979 | ||||||
| chr3:32757030
|
G | T | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596-2428G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757030 | ||||||
| chr3:32757048
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596-2410G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757048 | ||||||
| chr3:32757100
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-2358C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757100 | ||||||
| chr3:32757110
|
G | GA | 18 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0001g0119others(15): Show | 18 | HG01515.hp1 HG01517.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596-2332dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757110 | |||||
| chr3:32757142
|
A | G | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-2316A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757142 | ||||||
| chr3:32757170
|
A | ATT | 68 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0090others(65): Show | 68 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1596-2263_1596-226 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | |||||
| chr3:32757170
|
A | ATTT | 138 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1596-2264_1596-226 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | |||||
| chr3:32757170
|
A | ATTTT | 85 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0036others(82): Show | 85 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1596-2265_1596-226 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | |||||
| chr3:32757170
|
A | ATTTTT | 17 | a0001c0001t0001g0048a0001c0001t0001g0066a0001c0001t0001g0069others(14): Show | 17 | HG01517.hp1 HG01934.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-2266_1596-226 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | |||||
| chr3:32757170
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0002g0212a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG02630.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1596-2271_1596-226 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | |||||
| chr3:32757170
|
ATTTTTT | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(15): Show | 18 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596-2267_1596-226 others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | |||||
| chr3:32757203
|
G | A | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-2255G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757203 | ||||||
| chr3:32757365
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1596-2093G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757365 | ||||||
| chr3:32757398
|
C | T | 14 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(11): Show | 14 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596-2060C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757398 | ||||||
| chr3:32757443
|
T | C | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-2015T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757443 | ||||||
| chr3:32757469
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1596-1989G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757469 | ||||||
| chr3:32757479
|
A | G | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596-1979A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757479 | ||||||
| chr3:32757508
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-1950C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757508 | ||||||
| chr3:32757861
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1596-1597C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757861 | ||||||
| chr3:32757914
|
C | G | 1 | a0001c0001t0001g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1596-1544C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757914 | ||||||
| chr3:32757940
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-1518A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757940 | ||||||
| chr3:32758042
|
C | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-1416C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758042 | ||||||
| chr3:32758214
|
A | G | 23 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(20): Show | 23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596-1244A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758214 | ||||||
| chr3:32758347
|
C | G | 3 | a0001c0001t0001g0345a0001c0001t0001g0347a0004c0004t0001g0346 | 3 | HG01106.hp1 HG01109.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1596-1111C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758347 | ||||||
| chr3:32758626
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-832G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758626 | ||||||
| chr3:32758796
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1596-662C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758796 | ||||||
| chr3:32758811
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1596-647G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758811 | ||||||
| chr3:32758830
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-628C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758830 | ||||||
| chr3:32759045
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(51): Show | 54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1596-413A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759045 | ||||||
| chr3:32759130
|
A | AGTGT | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-307_1596-304d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32759130 | |||||
| chr3:32759130
|
AGT | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0078others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1596-305_1596-304d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32759130 | |||||
| chr3:32759130
|
AGTGTGTG others(1): Show |
A | 4 | a0001c0001t0001g0224a0001c0001t0001g0239a0001c0001t0001g0242others(1): Show | 4 | HG00408.hp2 HG02080.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-311_1596-304d others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32759130 | |||||
| chr3:32759131
|
G | T | 1 | a0001c0001t0001g0141 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1596-327G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759131 | ||||||
| chr3:32759132
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1596-326T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759132 | ||||||
| chr3:32759133
|
G | T | 1 | a0001c0001t0003g0327 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596-325G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759133 | ||||||
| chr3:32759134
|
T | A | 1 | a0001c0001t0003g0327 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596-324T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759134 | ||||||
| chr3:32759170
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596-288T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759170 | ||||||
| chr3:32759170
|
T | TATAC | 8 | a0001c0001t0001g0081a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG02647.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-270_1596-267d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32759170 | |||||
| chr3:32759173
|
AC | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-284delC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759173 | ||||||
| chr3:32759174
|
C | T | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-284C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759174 | ||||||
| chr3:32759247
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1596-211A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759247 | ||||||
| chr3:32759266
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1596-192G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759266 | ||||||
| chr3:32759681
|
A | G | 120 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1709+110A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32759681 | ||||||
| chr3:32759702
|
GAACGTTT others(3): Show |
G | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1709+135_1709+144d others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32759702 | |||||
| chr3:32759899
|
G | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0001g0231others(1): Show | 4 | HG02080.hp2 NA18953.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1709+328G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32759899 | ||||||
| chr3:32760008
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1709+437C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760008 | ||||||
| chr3:32760062
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0156a0001c0001t0001g0197 | 3 | HG02970.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1709+491A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760062 | ||||||
| chr3:32760070
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1709+499T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760070 | ||||||
| chr3:32760107
|
A | G | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1709+536A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760107 | ||||||
| chr3:32760128
|
G | GCCA | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1709+557_1709+558i others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760128 | ||||||
| chr3:32760130
|
T | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1709+559T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760130 | ||||||
| chr3:32760131
|
C | A | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1709+560C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760131 | ||||||
| chr3:32760133
|
CT | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1709+563delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760133 | ||||||
| chr3:32760179
|
C | CA | 10 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0340others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1709+622dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32760179 | |||||
| chr3:32760179
|
CA | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0030others(4): Show | 7 | HG00140.hp1 HG00408.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1709+622delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32760179 | |||||
| chr3:32760252
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1709+681T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760252 | ||||||
| chr3:32760270
|
C | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(51): Show | 54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1709+699C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760270 | ||||||
| chr3:32760305
|
C | T | 1 | a0001c0001t0003g0327 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1709+734C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760305 | ||||||
| chr3:32760473
|
A | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1709+902A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760473 | ||||||
| chr3:32760576
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1709+1005G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760576 | ||||||
| chr3:32760609
|
G | C | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1709+1038G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760609 | ||||||
| chr3:32760638
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1709+1067T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760638 | ||||||
| chr3:32760669
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1709+1098G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760669 | ||||||
| chr3:32760898
|
C | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1709+1327C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760898 | ||||||
| chr3:32760903
|
C | G | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1709+1332C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760903 | ||||||
| chr3:32761072
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1709+1501T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761072 | ||||||
| chr3:32761088
|
C | T | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1709+1517C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761088 | ||||||
| chr3:32761145
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1709+1574T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761145 | ||||||
| chr3:32761184
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0126a0001c0001t0001g0166 | 3 | HG02630.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1710-1549T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761184 | ||||||
| chr3:32761198
|
C | T | 103 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1710-1535C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761198 | ||||||
| chr3:32761518
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1710-1215G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761518 | ||||||
| chr3:32761590
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1710-1143C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761590 | ||||||
| chr3:32761604
|
G | GGAGTGCA others(39): Show |
1 | a0001c0001t0001g0080 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1710-1127_1710-108 others(50): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32761604 | |||||
| chr3:32761660
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1710-1073A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761660 | ||||||
| chr3:32761682
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1710-1051C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761682 | ||||||
| chr3:32761726
|
CT | C | 23 | a0001c0001t0001g0024a0001c0001t0001g0098a0001c0001t0001g0099others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1710-991delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32761726 | |||||
| chr3:32761726
|
CTT | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1710-992_1710-991d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32761726 | |||||
| chr3:32761758
|
A | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1710-975A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761758 | ||||||
| chr3:32761780
|
G | A | 103 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(100): Show | 103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1710-953G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761780 | ||||||
| chr3:32761791
|
CT | C | 10 | a0001c0001t0001g0204a0001c0001t0001g0227a0001c0001t0001g0250others(7): Show | 10 | HG01928.hp2 HG02015.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1710-937delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32761791 | |||||
| chr3:32761818
|
G | T | 105 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(102): Show | 105 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.1710-915G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761818 | ||||||
| chr3:32761829
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1710-904A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761829 | ||||||
| chr3:32761876
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0265 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1710-857G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761876 | ||||||
| chr3:32761899
|
A | G | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1710-834A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761899 | ||||||
| chr3:32761901
|
T | C | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1710-832T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761901 | ||||||
| chr3:32761933
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0197 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1710-800C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761933 | ||||||
| chr3:32762018
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1710-715A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32762018 | ||||||
| chr3:32762166
|
T | TA | 7 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0119others(4): Show | 7 | HG02809.hp2 HG04184.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1710-551dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32762166 | |||||
| chr3:32762239
|
G | A | 259 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1710-494G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32762239 | ||||||
| chr3:32762259
|
C | T | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1710-474C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32762259 | ||||||
| chr3:32762644
|
ATAATAAC others(16): Show |
A | 1 | a0001c0001t0001g0347 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1710-86_1710-64del others(23): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32762644 | |||||
| chr3:32762693
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1710-40C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32762693 | ||||||
| chr3:32763029
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1840+166G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763029 | ||||||
| chr3:32763157
|
G | C | 32 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.1840+294G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763157 | ||||||
| chr3:32763270
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1840+407A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763270 | ||||||
| chr3:32763338
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1840+475G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763338 | ||||||
| chr3:32763380
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1840+517G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763380 | ||||||
| chr3:32763456
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0320 | 2 | HG01928.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1840+593G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763456 | ||||||
| chr3:32763480
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1840+617G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763480 | ||||||
| chr3:32763506
|
A | G | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1840+643A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763506 | ||||||
| chr3:32763705
|
C | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1841-750C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763705 | ||||||
| chr3:32763714
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1841-741A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763714 | ||||||
| chr3:32763984
|
G | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1841-471G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763984 | ||||||
| chr3:32764058
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1841-397A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764058 | ||||||
| chr3:32764103
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0265 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1841-352G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764103 | ||||||
| chr3:32764138
|
A | C | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1841-317A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764138 | ||||||
| chr3:32764269
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG00558.hp2 NA18949.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1841-186G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764269 | ||||||
| chr3:32764336
|
C | CA | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1841-105dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 32764336 | |||||
| chr3:32764336
|
C | CAA | 13 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1841-106_1841-105d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 32764336 | |||||
| chr3:32764351
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1841-104G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764351 | ||||||
| chr3:32764351
|
G | T | 35 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(32): Show | 35 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1841-104G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764351 | ||||||
| chr3:32764815
|
T | A | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2004+6T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32764815 | ||||||
| chr3:32765018
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.2004+209A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765018 | ||||||
| chr3:32765028
|
A | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.2004+219A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765028 | ||||||
| chr3:32765036
|
T | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004+227T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765036 | ||||||
| chr3:32765037
|
T | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004+228T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765037 | ||||||
| chr3:32765243
|
G | A | 5 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004+434G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765243 | ||||||
| chr3:32765254
|
GTTGCAGT others(1308): Show |
G | 259 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2004+463_2004+1777 others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32765254 | |||||
| chr3:32765317
|
C | CA | 14 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.2004+521dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32765317 | |||||
| chr3:32765518
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2004+709G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765518 | ||||||
| chr3:32765646
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2004+837C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765646 | ||||||
| chr3:32765657
|
C | CA | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(18): Show | 21 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.2004+858dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32765657 | |||||
| chr3:32765658
|
A | C | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2004+849A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765658 | ||||||
| chr3:32765818
|
G | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.2004+1009G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765818 | ||||||
| chr3:32766003
|
AT | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG00733.hp1 HG01169.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2004+1213delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32766003 | |||||
| chr3:32766003
|
ATT | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0339a0001c0001t0001g0340others(10): Show | 13 | HG01071.hp2 HG01106.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2004+1212_2004+121 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32766003 | |||||
| chr3:32766024
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2004+1215A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766024 | ||||||
| chr3:32766027
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2004+1218C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766027 | ||||||
| chr3:32766035
|
C | T | 20 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.2004+1226C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766035 | ||||||
| chr3:32766088
|
C | G | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2004+1279C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766088 | ||||||
| chr3:32766118
|
G | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.2004+1309G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766118 | ||||||
| chr3:32766186
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 91 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2004+1377A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766186 | ||||||
| chr3:32766529
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2004+1720C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766529 | ||||||
| chr3:32766588
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.2004+1779G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766588 | ||||||
| chr3:32766608
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2004+1799G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766608 | ||||||
| chr3:32766622
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.2004+1813G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766622 | ||||||
| chr3:32766632
|
C | CA | 20 | a0001c0001t0001g0058a0001c0001t0001g0086a0001c0001t0001g0119others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.2004+1840dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32766632 | |||||
| chr3:32766677
|
G | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.2004+1868G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766677 | ||||||
| chr3:32766678
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.2004+1869C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766678 | ||||||
| chr3:32766796
|
T | C | 10 | a0001c0001t0001g0204a0001c0001t0001g0227a0001c0001t0001g0250others(7): Show | 10 | HG01928.hp2 HG02015.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004+1987T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766796 | ||||||
| chr3:32766824
|
A | T | 1 | a0001c0001t0001g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2004+2015A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766824 | ||||||
| chr3:32767028
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | NA18960.hp2 NA18962.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+2219G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767028 | ||||||
| chr3:32767316
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2004+2507C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767316 | ||||||
| chr3:32767377
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2005-2510G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767377 | ||||||
| chr3:32767427
|
G | T | 12 | a0001c0001t0001g0140a0001c0001t0001g0146a0001c0001t0001g0151others(9): Show | 12 | NA18943.hp2 NA18946.hp1 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.2005-2460G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767427 | ||||||
| chr3:32767442
|
G | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.2005-2445G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767442 | ||||||
| chr3:32767506
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2005-2381C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767506 | ||||||
| chr3:32767519
|
C | CA | 164 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2005-2350dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32767519 | |||||
| chr3:32767519
|
C | CAA | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.2005-2351_2005-235 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32767519 | |||||
| chr3:32767519
|
C | CAAA | 8 | a0001c0001t0001g0082a0001c0001t0001g0093a0001c0001t0001g0233others(5): Show | 8 | HG01258.hp1 HG01891.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.2005-2352_2005-235 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32767519 | |||||
| chr3:32767555
|
A | G | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005-2332A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767555 | ||||||
| chr3:32767616
|
G | A | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005-2271G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767616 | ||||||
| chr3:32767815
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2005-2072C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767815 | ||||||
| chr3:32767878
|
T | C | 1 | a0001c0001t0002g0322 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2005-2009T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767878 | ||||||
| chr3:32767903
|
G | A | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2005-1984G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767903 | ||||||
| chr3:32768320
|
A | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.2005-1567A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768320 | ||||||
| chr3:32768342
|
GA | G | 15 | a0001c0001t0001g0326a0001c0001t0001g0338a0001c0001t0001g0339others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2005-1544delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768342 | ||||||
| chr3:32768537
|
C | T | 8 | a0001c0001t0001g0081a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG02647.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005-1350C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768537 | ||||||
| chr3:32768583
|
C | CA | 54 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(51): Show | 54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2005-1292dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32768583 | |||||
| chr3:32768583
|
CA | C | 135 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(132): Show | 135 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.2005-1292delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32768583 | |||||
| chr3:32768616
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0316 | 2 | NA18953.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2005-1271C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768616 | ||||||
| chr3:32768654
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2005-1233A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768654 | ||||||
| chr3:32769073
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0110 | 2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2005-814T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769073 | ||||||
| chr3:32769162
|
G | A | 8 | a0002c0002t0001g0214a0002c0002t0001g0229a0002c0002t0001g0230others(5): Show | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005-725G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769162 | ||||||
| chr3:32769167
|
G | C | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2005-720G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769167 | ||||||
| chr3:32769179
|
C | A | 1 | a0001c0001t0003g0330 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2005-708C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769179 | ||||||
| chr3:32769427
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2005-460G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769427 | ||||||
| chr3:32769710
|
T | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(37): Show | 40 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.2005-177T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769710 | ||||||
| chr3:32769777
|
C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0326a0001c0001t0001g0338others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2005-110C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769777 | ||||||
| chr3:32769810
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2005-77G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769810 | ||||||
| chr3:32770067
|
A | AC | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | NA18961.hp2 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2080+107dupC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 32770067 | |||||
| chr3:32770194
|
G | T | 1 | a0001c0001t0001g0337 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2080+232G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770194 | ||||||
| chr3:32770317
|
AT | A | 63 | a0001c0001t0001g0087a0001c0001t0001g0103a0001c0001t0001g0107others(60): Show | 63 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.2080+381delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 32770317 | |||||
| chr3:32770317
|
ATT | A | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0027others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2080+380_2080+381d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 32770317 | |||||
| chr3:32770317
|
ATTT | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2080+379_2080+381d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 32770317 | |||||
| chr3:32770319
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2080+357T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770319 | ||||||
| chr3:32770388
|
C | T | 2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2080+426C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770388 | ||||||
| chr3:32770418
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2080+456C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770418 | ||||||
| chr3:32770537
|
C | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0326a0001c0001t0001g0338others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2080+575C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770537 | ||||||
| chr3:32770547
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.2080+585G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770547 | ||||||
| chr3:32770678
|
C | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.2080+716C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770678 | ||||||
| chr3:32770859
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.2080+897A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770859 | ||||||
| chr3:32770901
|
A | G | 17 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.2080+939A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770901 | ||||||
| chr3:32770964
|
C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0326a0001c0001t0001g0338others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2080+1002C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770964 | ||||||
| chr3:32770998
|
C | A | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2080+1036C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770998 | ||||||
| chr3:32771199
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2080+1237C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771199 | ||||||
| chr3:32771248
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2080+1286G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771248 | ||||||
| chr3:32771344
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2080+1382T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771344 | ||||||
| chr3:32771470
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2080+1508G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771470 | ||||||
| chr3:32771559
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2080+1597C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771559 | ||||||
| chr3:32771621
|
C | A | 1 | a0001c0001t0001g0338 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2080+1659C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771621 | ||||||
| chr3:32771625
|
T | C | 104 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(101): Show | 104 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2080+1663T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771625 | ||||||
| chr3:32771705
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2080+1743C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771705 | ||||||
| chr3:32771762
|
C | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2081-1695C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771762 | ||||||
| chr3:32771793
|
C | A | 63 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0084others(60): Show | 63 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2081-1664C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771793 | ||||||
| chr3:32771961
|
C | T | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2081-1496C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771961 | ||||||
| chr3:32772078
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.2081-1379C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772078 | ||||||
| chr3:32772091
|
A | C | 1 | a0001c0001t0001g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2081-1366A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772091 | ||||||
| chr3:32772096
|
A | C | 26 | a0001c0001t0001g0081a0001c0001t0001g0210a0001c0001t0001g0213others(23): Show | 26 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.2081-1361A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772096 | ||||||
| chr3:32772105
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2081-1352C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772105 | ||||||
| chr3:32772140
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2081-1317G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772140 | ||||||
| chr3:32772219
|
A | G | 3 | a0001c0001t0001g0255a0001c0001t0001g0260a0001c0001t0001g0262 | 3 | NA20752.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2081-1238A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772219 | ||||||
| chr3:32772230
|
G | C | 1 | a0001c0001t0001g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2081-1227G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772230 | ||||||
| chr3:32772292
|
T | C | 8 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2081-1165T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772292 | ||||||
| chr3:32772344
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(27): Show | 30 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.2081-1113G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772344 | ||||||
| chr3:32772438
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0352 | 3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2081-1019A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772438 | ||||||
| chr3:32772446
|
A | G | 1 | a0001c0001t0001g0353 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2081-1011A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772446 | ||||||
| chr3:32772474
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2081-983G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772474 | ||||||
| chr3:32772641
|
G | C | 1 | a0002c0002t0001g0272 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2081-816G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772641 | ||||||
| chr3:32772651
|
C | T | 7 | a0001c0001t0001g0345a0001c0001t0001g0347a0001c0001t0001g0348others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2081-806C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772651 | ||||||
| chr3:32772657
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2081-800A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772657 | ||||||
| chr3:32772704
|
A | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(27): Show | 30 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.2081-753A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772704 | ||||||
| chr3:32772966
|
A | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-491A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772966 | ||||||
| chr3:32772969
|
A | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-488A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772969 | ||||||
| chr3:32772970
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-487G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772970 | ||||||
| chr3:32772971
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-486C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772971 | ||||||
| chr3:32772972
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-485C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772972 | ||||||
| chr3:32773011
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2081-446A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773011 | ||||||
| chr3:32773038
|
G | T | 6 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0097others(3): Show | 6 | HG00099.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.2081-419G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773038 | ||||||
| chr3:32773056
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0109a0001c0001t0001g0120others(3): Show | 6 | HG00558.hp1 HG00673.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.2081-401G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773056 | ||||||
| chr3:32773207
|
A | G | 56 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(53): Show | 56 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.2081-250A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773207 | ||||||
| chr3:32773371
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2081-86A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773371 |